Addressing the reuse of lithium ion batteries (LIBs) extracted from used battery packs is an option for addressing environmental concerns. To guarantee their safety, the development of non-destructive analysis to identify LIBs exposed to over-discharge is mandatory. In this study, over-discharge-induced degradation in graphite/nickel cobalt aluminum oxide (NCA) lithium ion cells was investigated using differential voltage analysis (DVA) and electrochemical impedance spectroscopy (EIS). Two-stage cell capacity decay was solely observed in the deep over-discharge cycling at a lower cutoff voltage (LCV) of 1.00 V; in the first stage, the capacity gradually decreased similar to that at LCV >= 2.50 V, and then decreased steeply. In the over-discharge cycling, the DVA results confirmed that the electrode balancing between the anode and cathode contribute to increasing the cell capacity, whereas the cathode capacity decreased as cycling progressed, suggesting that electrode degradation induced by over-discharge is difficult to assess using the cell capacities. EIS analysis revealed that the charge-transfer resistance and interfacial capacitance of the NCA cathode changed markedly in the first stage under over-discharge. This study reports a meticulous characterization of over-discharge of LIBs using non-destructive electrochemical analysis and introduces a critical aspect for their detection before serious cell deterioration.

A low-resistance polypyrrole (PPy) film that can achieve high rates (rates of >1C) while suppressing polysulfide dissolution is developed in this study. To achieve high-rate characteristic in a sulfur cathode with high sulfur loading, a three-dimensional (3D) aluminum foam current collector is used and the Li+ concentration of the PPy film is enhanced by a glyme-Li equimolar complex as the polymerization electrolyte. A PPy-sulfur/ketjenblack (S/KB) 3D aluminum foam laminated cell with a sulfur loading of 5 mg cm(-2) is prepared. Consequently, a high discharge capacity of 794 mAh g(-1)-sulfur at 3.0C is achieved using 1 M lithium bis-(trifluoromethylsulfonyl)imide (LiTFSI) with dimethoxyethane (DME) and 1,3-dioxolane (DOL), (DME/DOL = 1/1 vol.) as the electrolyte and Li foil as the anode. In the cycling test, PPy-S/KB 3D Al foam cathode achieved a significant improvement in discharge capacity retention compared to bare S/KB 3D Al foam cathode without PPy coating. Moreover, almost no polysulfide dissolution is confirmed from the ultraviolet-visible spectrum of the electrolyte after the cycle evaluation. Here, we prepare a 3D structure S/KB cathode that can support high rates while suppressing sulfur dissolution by PPy coating, and reveal its potential for lithium-sulfur battery application.

In this study, the high-rate performance of high sulfur-loaded cathodes have been demonstrated using a novel battery that comprises of a 3 dimensional aluminum foam (current collector), sulfur (active material), acetylene black (conductive additive), and polypyrrole (PPy) coating. Consequently, a stacked laminated cell was prepared, which comprised of two 70 x 70 mm(2) PPy-sulfur/ketjen black sheets (sulfur loading = 4.3 mg/cm(2)), 1 M lithium bis-(trifluoromethylsulfonyl)imide (LiTFSI) with dimethoxyethane (DME) and 1,3-dioxolane (DOL), (DME/DOL = 1/1 vol%), and three Li foils as the cathodes, electrolyte, and anodes, respectively. The 1 M LiTFSI DME/DOL electrolyte, which is suitable for high rate, is applicable because the PPy coating suppresses dissolution of polysulfide into the electrolyte. The discharge capacities were 462 mAh (1075 mAh/g sulfur) at 0.4C (267 mA) and 251 mAh (583 mAh/g-sulfur) at 3.8C (2670 mA). An enhanced conductive path was formed in the cathode by the 3D Al foam and AB, which considerably improved the high-rate performance. This demonstration is particularly significant from the viewpoint of commercializing the high-power output and high-energy-density Li-S batteries for industrial applications such as small mobile device and drone power source. (c) 2020 Elsevier B.V. All rights reserved.

Lithium-ion capacitors (LICs) are energy storage devices that bridge the gap between electric double-layer capacitors and lithium-ion batteries (LIBs). A typical LIC cell is composed of a capacitor-type positive electrode and a battery-type negative electrode. The most common negative electrode material, graphite, suffers from low rate capability and cyclability due to the sluggish kinetics of the Li+ intercalation/de-intercalation process. In this work, metal chloride-pillared graphite, which has recently attracted attention as high-rate LIB anodes, is applied as the negative electrode for LICs for the first time to overcome this drawback. It is shown that AlCl3-graphite intercalation compounds (AlCl3-GICs) with a wide interlayer spacing benefit faster Li+ diffusion. The low molecular weight and conversion reaction of the AlCl3 pillar further enhance the specific capacity per mass. An optimized LIC cell composed of an AlCl3-GIC negative electrode and activated carbon as the positive electrode exhibited higher energy and power densities compared to LICs using graphite as the negative electrode, and displayed stable cycling performance with 85% capacity retention after 10 000 charge/discharge cycles. The AlCl3-GICs synthesized in this work displayed improved electrochemical performances and have the potential to replace the graphite electrode in conventional LICs.

Lithium-ion capacitors (LICs) operate by two mechanisms, namely a double-layer mechanism based on a capacitor-like positive electrode and the intercalation mechanism of a battery-like negative electrode. Hence, well-designed reaction kinetics between the positive electrode and negative electrode are essential for optimizing LIC full-cell configurations. In this study, we investigated the influences of fluoroethylene carbonate (FEC) or vinylene carbonate (VC) as electrolyte additives on full-cell performance of LICs. We confirmed that the internal resistance of graphite increased with the use of FEC, which degraded the cyclability of the LIC full-cell. Conversely, LICs consisting of the VC additive had good cyclability over 4000 cycles owing to the solid electrolyte interphase (SEI) containing polymeric species. This detailed investigation into the function of SEI compounds derived from VC additives and their effect on cyclability will provide new insights into optimization of LIC full-cell configurations with appropriate electrolyte additives.

Field effect transistor (FET) biosensors are capable of detecting various biomolecules, although challenges remain in the detection of uncharged molecules. In this study, the detection of uncharged cortisol was demonstrated by interfacial design using a technique to immobilize target-bound aptamers. The target-bound aptamers, which formed a higher-order structure than target-unbound aptamers, expanded the distance between adjacent aptamers and reduced the steric hindrance to the conformational change. The density-controlled aptamers efficiently induced their conformational changes with the cortisol binding, which resulted in the improvement of the sensitivity of FET biosensors. (C) The Author(s) 2020. Published by ECSJ.

In order to establish the universality of the excess heat production in electrochemical reaction, under a high magnetic field, as one of the most fundamental electrochemical reactions, the case of ferricyanide-ferrocyanide redox reaction was examined, where ionic vacancies with ± 1 unit charge were collided by means of magnetohydrodynamic (MHD) flow. As a result, from the pair annihilation of the vacancies with opposite signs, beyond 7 T, excess heat production up to 25 kJ·mol-1 in average at 15 T was observed, which was attributed to the liberation of the solvation energy stored in a pair of the vacancy cores with a 0.32 nm radius, i.e., 112 kJ·mol-1. Difference between the observed and expected energies comes from the small collision efficiency of 0.22 due to small radius of the vacancy core. Ionic vacancy initially created as a by-product of electrode reaction is unstable in solution phase, stabilized by releasing solvation energy. Ionic vacancy utilizes the energy to enlarge the core and stores the energy in it. As a result, solvated ionic vacancy consists of a polarized free space of the enlarged core surrounded by oppositely charged ionic cloud. The accuracy and precision of the measured values were ascertained by in situ standard additive method.

Secretory immunoglobulin A (s-IgA), found in biological fluids, is useful for monitoring condition on mental health to prevent depression. In this study, the non-invasive detection of s-IgA in human sweat was demonstrated using field effect transistor (FFT) bioscnsors modified with a plant lectin, jacalin, as a receptor. The s-IgA molecules were detected with greater sensitivity using the jacalin-immobilized FET biosensors as compared to the sensitivity shown by Fabimmobilized FET bioscnsors. Jacalin, which is a small lectin tetramcr, has four glycan-binding sites and can capture a large number of s-IgA molecules within the charge-detectable region in terms of Dcbye length. Moreover, the jacalin-immobilized FET bioscnsor could detect s-IgA at concentrations ranging from 0.1 mu g/ml. to 100 mu g/mL Additionally, by using a filtration process to eliminate the interference of other components found in human sweat, our FET sensing system could specifically and quantitatively detect s-IgA. Therefore, our results show the utility of this device in monitoring mental stress.

Coulombic efficiency (CE) has been widely used in battery research as a quantifiable indicator for the reversibility of batteries. While CE helps to predict the lifespan of a lithium-ion battery, the prediction is not necessarily accurate in a rechargeable lithium metal battery. Here, we discuss the fundamental definition of CE and unravel its true meaning in lithium-ion batteries and a few representative configurations of lithium metal batteries. Through examining the similarities and differences of CE in lithium-ion batteries and lithium metal batteries, we establish a CE measuring protocol with the aim of developing high-energy long-lasting practical lithium metal batteries. The understanding of CE and the CE protocol are broadly applicable in other rechargeable metal batteries including Zn, Mg and Na batteries.

Lithium sulfur batteries (LSBs) are regarded as promising electrochemical energy storage devices owing to their higher theoretical capacity than commercial cathode materials. Herein, we report a simple method for preparing a modified sulfur/Ketjenblack (S/KB) cathode using polymer composite poly(3,4-ethylenedioxythiophene)-poly (styrenesulfonate) (PEDOT:PSS), which displays ionic and electron conductivity and can suppress polysulfide dissolution during the charge-discharge process. The S/KB + PEDOT:PSS cathode displayed higher electrochemical performance than the S/KB cathode. The effectiveness of suppressing polysulfide dissolution was determined visually and by UV-visible spectroscopy. The findings demonstrate the multi-functionality of PEDOT:PSS as an efficient electron conductive additive for S/KB cathode in high-performance LSBs.

Prediction of degradation in lithium-ion batteries is critical to ensure battery safety. In this study, we report for the first time that electrochemical impedance spectroscopy (EIS) predicts serious capacity fade in lithium-ion batteries, which results from charge-discharge cycling under overcharge conditions. A nickel cobalt aluminum oxide (NCA) lithium-ion cell shows a two-stage capacity fade in the overcharge condition with an upper cutoff voltage (UCV) of 4.4 V. The capacity gradually decreases as cycling progresses (first stage), and then decreases steeply in the later cycles (second stage). Such a two-stage capacity fade is not observed when cell cycling in the appropriate voltage range (UCV <= 4.2 V). In the first stage, the cell capacities cycled at UCVs of 4.2 V and 4.4 V are approximately identical, with an inductively coupled plasma atomic emission spectrometry analysis confirming overcharge-induced deposition of Ni and Co on the anode surface. EIS analysis is used to model these deposited metals as enhanced impedance signals that represent the charge transfer resistance and interfacial capacitance of the anode in the first stage. This allows the advance prediction of overcharge-induced serious capacity decay in lithium-ion batteries to prevent cell destruction.

Electrochemical impedance spectroscopy has been widely used to understand the chemistry and physics of battery systems. This review covers electrochemical impedance spectroscopy used for the interpretation of impedance data of lithium-ion batteries (LIBs) from advanced equivalent circuit models to the mathematical model, which is developed by John Newman. In addition, as a method to realize an energy-sustainable society using diagnostics based on the combination of LIBs and electrochemical impedance spectroscopy, on-board diagnostics of battery packs are achieved based on an input signal generated by a power controller in a battery management system instead of the conventionally used frequency response analyzer. The diagnostic system is applicable to energy management systems which are installed in homes, buildings, and communities, accumulating the impedance data on state of health of LIBs. Finally, a future possibility regarding the diagnostics of battery packs coupled with the machine learning of impedance data is introduced.

A Lithium-ion capacitor (LIC) is composed of an electrochemical capacitor-like cathode and battery-like anode which store charge based on non-faradaic and faradaic processes, respectively. As an anode material for LIC, graphite is widely used because of its physical and electrochemical advantages. In the LIC system, stable cyclability at the high rate conditions is essential for bridging the gap between lithium-ion batteries and supercapacitors. However, there have been reported that the low working potential of graphite (close to 0.05 V vs Li/Li+) causes Li plating on the graphite surface and non-unity coulombic efficiency at high current charge/discharge results in degradation of cycle performance. To overcome this issue, stacked reduced graphene oxide-tin (SrGO-Sn) composite by co-reduction of graphene oxide and Sn2+ are studied in this work. The LIC consisting of SrGO-Sn anode shows good long-term cyclability with a remarkable capacity retention of 85, 77, and 60% at 10,000, 50,000, and 100,000th cycle and coulombic efficiency of 98% after 120,000 cycles. We believe that this study presents a new approach to the design of the high-performance LIC using an alternative to conventional graphite-based anode materials. (c) 2020 The Electrochemical Society ("ECS"). Published on behalf of ECS by IOP Publishing Limited.

Lithium-ion capacitors (LICs) have been attracting research interest over the past years as promising electrochemical energy devices because they show higher energy densities than supercapacitors and higher power densities than batteries. In this study, we synthesized an Sn-Ni alloy by electrodeposition and applied it as an anode for LICs. To optimize the full-cell configuration, we controlled the mass balancing between the loading amounts of active materials in the cathode and anode with different mass ratios of 16:1, 8:1, and 4:1. In addition, the Sn-Ni alloy was investigated using electrochemical impedance spectroscopy under different depth of discharge (DOD) levels. The LICs assembled with a mass ratio of 4:1 between the cathode and anode exhibited good cyclability, rate performance, energy, and power density. This study not only improved the cycle performance of LICs full cell by mass balancing, but also revealed the relationship between the electrochemical characteristics of LICs and DOD levels of the Sn-Ni anode.

Tin-nickel (Sn-Ni) alloy is a promising candidate as an anode for the lithium-ion capacitor (LIC) because it is superior in volumetric energy density compared with that of the graphite anode. However, its cycle durability requires improvement, even with a higher utilization ratio of the anode. The effect of lithium salts, LiPF6 and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) is investigated for usage in the LIC in severe conditions (utilization ratio of the anode: 20%). The LIC with LiTFSI delivered its initial capacity up to similar to 400 cycles, which is 4 times longer than the LIC with LiPF6. The reason for the capacity decay in the LiPF6 system is attributed to the narrowing of the potential range of the activated carbon cathode due to a widening potential range of the Sn-Ni alloy anode during operation. This widening is attributed to the loss of the active material due to peeling-off from the substrate. However, when LiTFSI is used, no such decay is observed. It is suggested that a polymer-like solid electrolyte interphase derived from TFSI- may suppress the loss of the active material. This finding can encourage the development of an Sn-based anode for LICs in combination with a mild operating condition and electrolyte additives. (C) The Electrochemical Society of Japan, All rights reserved.

Lithium sulfide (Li2S) is considered to be a promising cathode material for safer energy storage cells due to its compatibility with Li metal-free anodes. However, challenges remain regarding the insulating nature of Li2S, which leads to poor electrochemical performance, currently making Li2S electrodes far from practical in real-world applications. Herein we present a chemical method to synthesize Li2S nanoflake wrapped carbon material, Ketjenblack (LS@KB) composite, which can be coated on different current collectors without the addition of a binder. The high contact area between KB nanoparticles and Li2S nanoflakes effectively improves the cathode's conductivity, which contributes to a high Li2S weight ratio (83%). In addition, we prove that the well wrapped LS@KB structure enhances the physical confinement of polysulfides, leading to improved cyclability. As a result, the synthesized LS@KB cathode delivers stable cyclability (1000 cycles) with a fading rate of 0.03% per cycle at 0.5 C-rate. This room temperature fabrication strategy conquers the major drawbacks existing in Li2S fabrication, such as high temperature, hazardous gas release, complex and high-cost production process, making it a promising cathode material for light and safe portable electronic devices. (C) 2020 The Electrochemical Society ("ECS"). Published on behalf of ECS by IOP Publishing Limited.

A solvate ionic liquid (SIL) of highly concentrated 4.0 M lithium nitrate (LiNO3) in a dimethylsulfoxide solution is introduced for lithium-oxygen batteries. As a redox mediator (RM), highly concentrated LiNO3 in the SIL works more effectively than the lower concentrated one to decompose lithium peroxide (Li2O2) on the cathode with an extremely low charging voltage of 3.6 V. In addition, X-ray photoelectron spectroscopy analysis confirms that side products during discharging and charging are markedly restricted in the SIL. The low solubility of Li2O2 intermediate (LiO2) in the SIL may be an important reason for the restriction of side products. (C) The Author(s) 2019. Published by ECS.

Lithium-ion capacitors (LIC) constructed by combining a supercapacitor-like cathode and battery-like anode are expected to bridge a gap between low power density from lithium-ion batteries (LIB) and low energy density from the supercapacitors. In this study, we synthesize the Sn-Ni alloy by electrodeposition in the aqueous solution as an anode for LIC. The lower volume expansion rate of Sn-86 than pure Sn anode can be confirmed by in-operando investigation using an optically transparent cell during the 1st charging process. This is attribute to the co-deposited Ni can act as a buffer matrix to restrain volume expansion. For the full-cell test, the pre-lithiation condition of Sn-Ni was investigated with different depth of discharge levels. As a result, a LIC consisting of activated carbon (AC) cathode and Sn-86 exhibits a good cyclability for 3000 cycles with a capacity retention of 80% and coulombic efficiency of 98% at 3000th cycle. The Sn-Ni//AC LIC shows improved volumetric energy and power density than graphite//AC LIC. This study presents a new possibility of Sn-Ni alloy as an anode for the improved electrochemical performance of LIC. (C) 2019 The Electrochemical Society.

The silicon-based composite prepared by electrodeposition exhibits outstanding electrochemical performances for several thousand cycles because the co-deposited oxygen and carbon could act as buffer materials to reduce internal stress during charge-discharge cycling. However, it is not easy to increase the loading amount of active materials due to low structural stability at a high passing charge over 15 C cm(-2) for electrodeposition, leading the low areal capacity of Si-O-C composite as an anode. In this study, we propose a new way to enhance the structural stability of silicon-based anode by an electrochemical co-deposition technique using tin as supporting material, namely Sn-Si-O-C composite. The co-deposited tin has a whisker-shaped structure, and it prevents the exfoliation of activated material during electrodeposition. Besides, tin whisker can act as an electron pathway, resulting in improved electrochemical performance including high rate performance. The enhanced electrical conductivity is investigated by electrochemical impedance analysis. The improved electrochemical performance of Sn-Si-O-C composite indicates the high potential as an electrode material for high-performance lithium-ion batteries.

In this work, we present a powdered Si-O-C composite, namely pSi-O-C composite, synthesized by electrodeposition harvesting method. This new type of the Si-O-C composite shows impressive results, such as outstanding cyclability with a good discharge capacity of 616 mAh g(-1) which reached 10,000 cycles, and a remarkable coulombic efficiency of 99% at the 10,000th cycle. Furthermore, the pSi-O-C composite demonstrates the highest amounts of loaded silicon compared to different types of Si-O-C composite deposited on a Cu and CNTs/Cu substrate. (C) 2019 Elsevier B.V. All rights reserved.

Pandemic influenza, triggered by the mutation of a highly pathogenic avian influenza virus (IFV), has caused considerable damage to public health. In order to identify such pandemic IFVs, antibodies that specifically recognize viral surface proteins have been widely used. However, since the analysis of a newly discovered virus is time consuming, this delays the availability of suitable detection antibodies, making this approach unsuitable for the early identification of pandemic IFVs. Here we propose a label-free semiconductor-based biosensor functionalized with sialic-acid-containing glycans for the rapid identification of the pandemic IFVs present in biological fluids. Specific glycans are able to recognize wild-type human and avian IFVs, suggesting that they are useful in discovering pandemic IFVs at the early stages of an outbreak. We successfully demonstrated that a dual-channel integrated FET biosensing system, which were modified with 6'-sialyllactose and 3'-sialyllactose for each gate area, can directly and specifically detect human H1N1 and avian H5N1 IFV particles, respectively, present in nasal mucus. Furthermore, to examine the possibility of identifying pandemic IFVs, the signal attributed to the detection of Newcastle disease virus (NDV) particles, which was selected as a prime model of a pandemic IFV, was clearly observed from both sensing gates. Our findings suggest that the proposed glycan-immobilized sensing system could be useful in identifying new pandemic IFVs at the source of an outbreak.

Here we report an 'injection' strategy to introduce transportable Li-ion in the metallic Li free sulfur-graphite (S-G) pouch type full cell, which could alleviate the safety issues from Li dendrites. A novel process with organo-lithium reagent is used to reduce S to Li2S rapidly during assembling the pouch type full cell. The sublimation property of the side product enables the in-situ injection in the pouch type cell, which will not introduce impurities. In addition, this 'injection' strategy avoids the drawbacks from the instability of the Li2S to moisture, which could largely reduce the production cost and improve the practical energy density of the cell. The injected Li2S-G battery shows quite stable cyclability with a capacity of 640 mAh g(-1) at 0.1 C rate. This in-situ 'injection' method provides an effective and practical way to produce Li metal free sulfur Li-ion battery with alleviated safety issues.

Li-ion capacitors (LIC) which bridge the advantages of supercapacitors and Li-ion batteries have attracted a great deal of attention as a promising energy storage device. In this study, we synthesize the Si-O-C by electrodeposition at low levels of electricity below 2.0 C cm(-2) as an anode for LIC. The deposited Si amounts are controlled by charge density during electrodeposition from 0.3 to 1.0 C cm(-2). The material and electrochemical characteristics of Si-O-C fabricated at a charge density of 1.0 C cm(-2) are studied. The LIC consisting of Si-O-C anode shows an encouraging 95% retention of the initial capacity after 1000 cycles. In addition, the LIC shows a capacity retention ratio of 94% at 140 C-rate. This study reveals the potential prospect to use Si-O-C fabricated by electrodeposition as an anode for a high-rate capability for LIC. (C) The Author(s) 2019. Published by ECS.

Herein, we synthesized the structural stabilized Si-O-C composite using carbon nanotubes (CNTs). The SiO-C/CNTs is employed and tested as an anode for lithium-ion batteries (LIBs) assembled with the LiCoO2 cathode. Through the usage of CNTs, it is possible to improve the cyclability and capacity retention ratio by enhanced structural stability. The enhanced electrochemical performance of LiCoO2//Si-O-C full-cell with CNTs indicates the high potential as a way to produce the high-performance LIBs. (C) 2019 Elsevier B.V. All rights reserved.

In order to obtain highly ordered L1(0)-FePt nanoparticles for hard disk drive applications, the L1(0)-phase transformation of chemically synthesized FePt nanoparticles deposited on a naturally oxidized Si substrate was investigated using rapid thermal annealing. The heating and cooling rates during annealing were changed logarithmically with a constant annealing temperature (800 degrees C) and holding time (10 min). Almost completely ordered L1(0)-FePt nanoparticles were confirmed by grazing incidence X-ray diffraction measurements, irrespective of the heating and cooling rates, and the amount of the silicide changed in response to both. Nearly pure L1(0)-FePt was obtained when rapid heating (more than 780 K/min) and rapid cooling (more than 290 K/min) were applied. L1(0)-FePt degraded into Fe3Si and PtSi when the cooling rate was lower than 7.8 K/min. Rapid heating as well as rapid cooling of FePt nanoparticles can provide a facile route for the high-throughput production of L1(0)-FePt-based high-density magnetic recording media. (c) 2019 The Electrochemical Society.

The thermal runaway of a lithium ion battery (LIB) during a nail-penetration test was investigated using an LIB internal short circuit observation system equipped with an X-ray scanner (LiSC scanner). Using high-speed moving images and high-precision voltage measurements, the layer-by-layer internal short circuit caused by the nail was clearly observed during nail motion. Following this motion, gas generation outside the cell, which is well-known in thermal runaway, was observed. The main causes of smoke are speculated to be the boiling of the electrolyte and/or decomposition of the active materials owing to heating by the short circuit current. The initial behavior of the short circuit before gas generation was clearly observed. Therefore, gas generation, which is well-known to indicate an internal short circuit of the cell, and the electrical behavior of the short circuit during the nail-penetration test were observed separately. This LiSC scanner allowed us to analyze the details of the internal short circuit of the cell, and it is expected to lead to significant advancements in the safety of LIBs. (c) The Author(s) 2019. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited.

We describe a facile and simple solid-state thermolysis route for the preparation of Co, Ni, and Fe phosphide nanoparticles embedded in amorphous carbon using an organometallic complex. This was achieved by using a suitable organometallic complex in a single step synthetic route without using any solvent or catalyst. The advantage of using such precursor was to offer a source for metal, phosphorus and carbon without using any additional sources. The morphology of products was characterized by transmission electron microscopy, scanning electron microscopy and nature of carbon was analyzed using the Raman microscope and X-ray diffraction. The electrocatalytic oxygen evolution reaction (OER) activity and stability of the metal phosphide nanostructure was evaluated using the rotating disk electrode technique. The CoP, NiP and FeP exhibit the OER overpotential of 370, 380 and 550 mV at 10 mA cm(-2), respectively in 0.1 M KOH electrolyte. Among prepared phosphide catalysts, cobalt phosphide shows a lowest Tafel slope indicate favorable kinetics for the OER activity than nickel and iron phosphide catalysts. (C) 2018 Elsevier Ltd. All rights reserved.

Lithium-ion batteries are required to have high-power density, that is to reduce impedance, for use in electric vehicles. This paper focuses on interfacial resistance between the cathode layer (CL) and the current collector (CC) observed at high frequencies, which is generally attributed to a resistance of surface film like SEI. To investigate the interfacial resistance systematically, different interfaces between the CL and the CC were prepared by controlling the press rate for the cathode preparation, or by introducing a carbon under-coating layer (CUL), followed by electrochemical impedance spectroscopy (EIS). The interfacial resistance between the CL and the CC prepared with an insufficient press rate or without a CUL was extremely high for the entire cathode. From the cathode cross-sectional observation, it was observed that this high interfacial resistance was caused by low contact rate at the interface. Using a pouch-type symmetric cell, EIS revealed that the interfacial resistance is attributed to electric resistance, that is, contact resistance at the interface. Also, the other resistances were attributed to be the ionic resistance of the electrolyte and pores in the cathode, and the charge transfer resistance of the cathode. Furthermore, the effectiveness of the CUL was shown to decrease the cathode impedance.

A system using a high-speed and high-precision X-ray inspection system for testing internal short circuits in lithium-ion batteries (LIBs) was firstly developed for the safety test on LIBs. X-ray transmission moving images of the anode and cathode were obtained in the layered LIB structure. The nail-penetration test was chosen to test for the presence of an internal short circuit. This system would allow direct observation of smoke generation inside outside the battery, ballooning of the pouch, as well as changing layered structures of electrodes in real time. Since the results of a conventional nail-penetration test are indicated only by smoke generation, fire, or explosion, this new system allows electrode changes in the pouch to be observed for the first time. This system is expected to lead to great developments in the safety of LIBs.

Among the recent advancements in lithium-oxygen (Li-O-2) chemistries, redox mediators (RMs) have been revealed to play a significant role in decreasing overpotential on charging and in improving cycling performance. However, an intrinsic problem is redox shuttle of RMs, which leads to degraded RM utilization and induces the accumulation of discharge products on the cathode surface; this remains a significant issue in the current battery cell configuration (Li anode/separator/cathode). To address this detrimental problem, herein we propose a novel Li-O-2 cell incorporating a freestanding electropolymerized polypyrrole (PPy) film for the restriction of the redox-shuttle phenomenon of lithium iodide (Li anode/separator/PPy film/cathode). In this study, a PPy film, which is prepared through oxidative electropolymerization using an ionic liquid of 1-methyl-1-butylpyrrolidinium mixed with pyrrole and lithium bis(trifluoromethanesulfonyl) imide, is introduced between the cathode and the separator. From the charge-discharge voltage profile, it is confirmed that the PPy film suppresses the diffusion of the oxidized I-3(-) to the Li anode, while allowing Li ion transport. Secondary scanning electron microscope measurements confirm that the chemical reactions between I-3(-) and Li2O2 are facilitated by the presence of the PPy film because I-3(-) remains near the cathode surface during the charging process. As a result, the cycling performance in the Li-O-2 cells with PPy film exhibits a cycling life four times as long as that of the Li-O-2 cells without PPy film. (C) 2018 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license.

As amyloid-β peptide 1–42 (Aβ42) was found to be an emerging and important biomarker for Alzheimer's disease, the detection of this peptide in biological samples such as human serum (HS) has become very important for evaluating the potential disease state and determining the appropriate treatment. In this study, we developed an electrical analysis strategy based on a field effect transistor (FET) biosensor as a simple and reliable technique for confirming the presence of Aβ42 aggregates (fibrils) in biological samples. By utilizing Congo red immobilized on the FET gate surface as a biorecognition element, we observed remarkable sensitivity and specificity for detecting Aβ42 fibrils. Furthermore, we optimized the procedure to minimize the interference of abundant human serum albumin for the detection system using HS samples. The optimized system of Congo red-immobilized FET enables measurement of Aβ42 fibrils in the 100-pM level in HS samples, which is lower than its clinical concentration. The FET device can be applied as a biosensing system for mass and routine screening of peptide biomarkers related to Alzheimer's disease.

Recent statistics show that the incidence and mortality of cancer are on the rise. Among all types of cancer, lung cancer and liver cancer arc the most prevalent. We have many biomarkers for these two cancers, among which the cytokeratin fragment 21-1 (CYFRA 21-1) and a-fetoprotein (AFP) are the most common and widely used. Among the various detection methods, the field effect transistor (FET) biosensor is one of the most attractive approaches, providing a label-free, fast, and low-cost electrical detection of biomarkers with high specificity and sensitivity. In previous work, we applied biomarkers for a single cancer type. With the detection of CYFRA 21-1 and neuron-specific enolase (NSE), lung cancer was differentiated in the early stages. Compared with the early work, the biomarkers for the two cancer types, CYFRA 21-1 for lung cancer and AFP for liver cancer, were prepared in this work. The detection of CYFRA 21 1 and AFP in human serum was achieved at the same time with the limits of detection of 1 and 10 ng mL(-1), while the cut-off values were 4 and 10 ng mL(-1). The method featured short analytical time, small sample volume, and low cost. With its good selectivity and appropriate sensitivity, clinical application will become popular in the future.

In recent years, food safety concerning food allergy has received increasing attention globally. A simple and sensitive detection method should be developed to measure trace amounts of allergens in foods. Here, we propose a label-free field effect transistor (FET)-based biosensing system for the detection of a buckwheat allergenic protein, BWp16, by surfactant-induced signal amplification. BWp16 could be detected by coupling with an anionic surfactant, sodium dodecyl sulfate (SDS), as this coupling enhanced the net charge of the protein, enough to be detected by FET biosensors. A significant response was observed when the allergen was coupled with SDS, while the responses were decreased or unchanged when it was coupled with a cationic or non-ionic surfactant, suggesting that the SDS coupling maintains the antibody recognition ability of the target allergen, and it would be useful to enhance the sensor responses. The fluorescence spectroscopic measurement revealed that the SDS molecules were successfully coupled with target allergenic protein BWp16, resulting in an increase in its net charge. Furthermore, we demonstrated that the FET biosensor enables specific detection of the allergen in food at the desired concentration levels for food safety analysis, suggesting that it could be used as an alternative food allergen analyzer, both industrially and domestically. (C) 2017 The Authors. Published by Elsevier B.V.

With the objective of finding an avenue for development of magnetic hyperthermia as an effective mesothelioma treatment, the influence of heating by magnetite nanoparticles (MNPs) with a diameter of ~40nm, which were incorporated into cells and then subjected to AC magnetic field, on induction of cell death was investigated in all three histological subtypes of human mesothelioma cells (i.e., epithelioid NCI-H28, sarcomatoid NCI-H2052, and biphasic MSTO-211H cells). Cellular uptake of MNPs was observed in all cell types, but the amount of MNPs incorporated per cell into MSTO-211H cells was smaller than in NCI-H28 and NCI-H2052 cells. On the other hand, cell death induced by cellular uptake of MNPs was observed specifically in MSTO-211H cells. Hence, when cells are heated by intracellular MNPs under AC magnetic field, a high degree of cell mortality in NCI-H28 and NCI-H2052 cells is induced by the temperature increase derived from the high amount of intracellular MNPs, but the combination of intracellular heating and cell-type-specific toxicity of MNPs induced high rates of cell death in MSTO-211H cells even at a lower temperature. Almost all of the heated cells were dead after 24-h incubation at 37°C in all histological subtypes. Additionally, higher mortalities were observed in all three types of mesothelioma cells after MNPs-heating, as compared to the heating with a thermostatic bath. Herein, the significance of cellular uptake of MNPs for effectively inducing cell death in mesothelioma has been demonstrated in vitro.

The controlled design of biosensors based on the photo-electrochemical technique with high selectivity, sensitivity, and rapid response for monitoring of mono-bioactive molecules, particularly dopamine (DA) levels in neuronal cells is highly necessary for clinical diagnosis. Hierarchical carbon-, nitrogen-doped (CN) nickel oxide spear thistle (ST) flowers associated in single-heads (S), and symmetric and asymmetric-double heads (D and A, respectively) that are tightly connected through a micrometric dipole-like rod or trunk were fabricated by using a simple synthetic protocol. The CN-ST flower heads were decorated with dense nano-tubular like hedgehog needle skins in vertical alignments. These designated architectures are key features for creating biosensor surface electrodes for photo-electrochemical, ultrasensitive screening of mono-bioactive molecules. The exceptional electrode designs produced numerous catalytically active sites, large surface area, and high electron-transfer mobility. The active coating of carbon-nitrogen nanospheres significantly enhanced the photo-electrocatalytic activity of the prepared biosensor electrodes and prevented leakage of photocatalytic activity under long-term exposure to irradiation. Among all photo-electrochemical assays, the biosensors showed significant sensitivity and selectivity for DA in the presence of interfering molecules such as ascorbic acid (AA), uric acid (UA), adrenaline (A), and noradrenaline (NA). The photo-electrochemical property of the CN-SST-{110} crystal surface electrode showed significant sensing performance for DA in terms of unimpeded diffusion pathways, a wide concentration-detection range, and a low detection limit, even in the presence of potentially interfering molecules compared with other electrode-modified CN-DST-{111} and CN-AST-{101} crystal surfaces. Furthermore, the CN-SST photo-biosensor electrode shows potential in the selective and sensitive determination of DA in real samples, such as human serum and secreted DA from living cells. This finding indicates that the hierarchical ST biosensor may enable analytical discrimination and monitoring of DA and can be employed for clinical diagnosis application.

This work reports a new chemical pre-lithiation method to fabricate lithium sulfide (Li2S) cathode. This pre-lithiation process is taken place simply by dropping the organolithium reagent lithium naphthalenide (Li(+)Naph(-)) on the prepared sulfur cathode. It is the first time realizing the room temperature chemical pre-lithaition reaction attributed by the 3D nanostructured carbon nanotube (CNT) current collector. It is confirmed that the Li2S cathode fabricated at room temperature showing higher capacity and lower hysteresis than the Li2S cathode fabricated at high temperature pre-lithiation. The prelithiated Li2S cathode at room temperature shows stable cycling performance with a 600 mAh g(-1), capacity after 100 cycles at 0.1 C-rate and high capacity of 500 mAh g(-1) at 2 C-rate. This simple on -site prelithiation method at room temperature is demonstrated to be applicable for the in-situ pre-lithiation in a Li metal free battery. (C) 2017 The Authors. Published by Elsevier B.V.

The concept of unobtrusive physiological balance sensing system implementing biosensors is discussed. Biosensors connected with a data system are expected to play a significant role when we extend the sensing objects from body to mind and spirit. Here, we describe the unobtrusive monitoring system using field effect transistor-type sensors and wireless communication devices. Substances subject to the survey of our research will include small ions, immunoglobulins, and hormones. (C) 2017 Wiley Periodicals, Inc.

Electrochemical impedance measurements of lithium ion batteries (LIBs) in energy storage systems (ESS) were performed. Square-current electrochemical impedance spectroscopy (SC-EIS), which is a simple and cost-effective approach to measure impedance, was chosen to investigate a large-scale LIB system. Harmonics calculated by Fourier transform from a square waveform were used to determine the impedance. On the basis of a simple electrochemical reaction involving the ferri/ferro-cyanide redox couple and the LIB, the accuracy of the impedance measurement was found to depend on both the signal-to-noise ratio of the power spectra of the harmonics as well as the attenuation rate of the "measured value of impedance" and the "theoretical spectra value" from Fourier series. The accuracy was improved by adjusting the input waveform to be close to an ideal square waveform from Fourier series. The accuracy was further improved by the combined use of a simple moving average and an overall average. The impedance from a degraded square waveform generated by a cost-effective power controller was able to be determined by increasing the measurement time, which aided averaging. By designing the input signal to be close to an ideal square waveform from Fourier series, kilowatt-class LIB modules/cubicles in an ESS was able to be measured. Moreover, a degraded LIB module in an ESS was able to be detected using EIS, which highlights the utility of this technique for in situ impedance measurements of large-scale LIB systems. (C) 2017 Elsevier Ltd. All rights reserved.

The cycle durability of electrodeposited Si-O-C composite anodes in glyme-based ionic liquid electrolytes, known as Li(G3)TESI or Li(G4)TFSI (triglyme: G3 and tetraglyme: G4), which is one of the most promising electrolytes for sulfur cathode, was improved for use in lithium secondary batteries by using additives, fluoroethylene carbonate (FEC) or vinylene carbonate (VC). We revealed an importance of the activation process and the effects of additives in the Si-O-C composite anode. The capacity of the Si-O-C composite anode decreased with charge-discharge cycles in electrolytes without additives. Meanwhile, although the capacity retention in electrolytes with additives was improved by 10-20%, their initial capacity was smaller than those without additives. To solve the contradiction, an activation process, in which the Si-O-C composite anode was charged and discharged in electrolytes without additives, was introduced before charge-discharge cycles in electrolytes with additives. Owing to the optimized activation process, the initial capacity in electrolytes with additives showed as high as 1100-1300 mAh(-1) as those without additives with better capacity retention. Therefore, the necessity to adequately generate an activation reaction and to form SEI derived from additives for the Si-O-C composite anode to have better charge-discharge performance was demonstrated. (C) 2017 Elsevier Ltd. All rights reserved.

Mid to low frequency impedance for a cathode in a lithium ion battery (LIB), which is affected by lithiumion diffusion into active materials, was investigated. We had earlier suggested that charge-transfer and diffusion impedances are attributed to a particle size distribution for a commercially available LIB, and we designed an equivalent circuit in which two series circuits of charge-transfer resistance and Warburg impedance were connected in parallel. Here, to validate the design of the equivalent circuit, the secondary-particle size distribution of the LiNi1/3Mn1/3Co1/3O2 cathode in a lab-made LIB, in which the secondary-particles were controlled into wide and narrow distribution by sieving, was investigated by electrochemical impedance spectroscopy. The equivalent circuit was designed in which series circuits of charge-transfer resistance and Warburg impedance were connected in parallel. Dependency of impedance response on the number of parallels of the series circuits was evaluated for the cathodes using different secondary-particle size distributions of the active material. Additionally, the tendency of change in the charge-transfer resistance and the limiting capacitance was discussed from the standpoint of secondary-particle size distribution. The results confirm the effectiveness of the designed equivalent circuit which reflects the secondary-particle size distribution of cathode active materials. (C) 2017 Elsevier Ltd. All rights reserved.

An increased penetration of wind energy into the power system will lead to instability of local voltage and global frequency in Japan. Power flow simulation is a powerful tool for understanding the electrical behavior in the power system caused by wind energy; however, plausible and various wind power profiles are required to perform a meaningful simulation to evaluate the effect of wind generators. This paper proposes a procedure of generating synthetic wind power profiles that involve the plausible short-term fluctuation for a power flow simulation based on the spatial kriging method and the bootstrap method. (C) 2016 American Society of Civil Engineers.

Lithium metal free sulfur battery paired by lithium sulfide (Li2S) is a hot point in recent years because of its potential for relatively high capacity and its safety advantage. Due to the insulating nature and high sensitivity to moisture of Li2S, it calls for new way to introduce Li ion into S cathode besides the method of directly using the Li2S powder for the battery pre-lithiation. Herein, we proposed a pre-lithiation method to lithiate the polypyrrole (PPy)/S/Ketjenblack (KB) electrode into PPy/Li2S/KB cathode at room temperature. By this process, the fully lithiated PPy/Li2S/KB cathode showed facilitated charge transfer than the original PPy/S/KB cathode, leading to better cycling performance at high C-rates and disappearance of over potential phenomenon. In this work, the ion-selective PPy layer has been introduced on the cathode surface by an electrodeposition method, which can suppress the polysulfide dissolution from the cathode source. The lithium metal free full battery coupled by the prepared Li2S/KB cathode and graphite anode exhibited excellent cycling performance. Hence, we believe this comprehensive fabrication approach of Li2S cathode will pave a way for the application of new type lithium metal free secondary battery. (C) 2016 Elsevier B.V. All rights reserved.

Degradation of lithium-ion battery (LIB) was evaluated by using liquid chromatography-quadruple time of flight mass spectroscopy (LC-QToF/MS). Lab-made LIBs were degraded by storing at their states of charge of 50% at 25 or 60 degrees C for three months. The degradation of the LIB was accelerated at 60 degrees C compared with that at 25 degrees C. The electrochemical impedance spectroscopy analysis suggested that the remarkable degradation occurred for solid electrolyte interphase (SEI): it was implied that on one hand, the composition of the SEI for the LIB degraded at 25 degrees C did not vary, on the other hand, that at 60 degrees C varied. For LC-QToF/MS analysis, although decomposed products derived from the electrolyte solution were detected from the electrolyte in the LIB degraded at both 25 and 60 degrees C, those decomposed products were almost the same. Whereas, the difference between decomposed products at 25 and 60 degrees C was confirmed for the interphases between electrodes and electrolyte. The characteristic decomposed products at 60 degrees C was a product with more than C35 and more than 500 m/z of mass number. This product should be one of the reason of capacity degradation due to the internal resistance increase. Thus, a possibility of LC-QToF/MS was demonstrated. (C) The Electrochemical Society of Japan, All rights reserved.

A high areal capacity lithium-sulfur battery making use of mass produced aluminum metal foam as a current collector was investigated. A sulfur/Ketjenblack (KB) composite was filled and deposited into the aluminum foam current collector via a predetermined filling procedure, resulting in high sulfur loading. The value for this loading was found to be 17.7 mg sulfur/cm(2) by using carboxymethyl cellulose and styrene butadiene rubber (CMC + SBR) as a binder. An operating single-layer pouch-type cell with an S/KB+CMC+SBR on Al foam cathode was created as a result of this synthesis and found to possess an unprecedentedly high areal capacity of 21.9 mAh/cm(2). On the basis of the achieved areal capacity, the energy density of a theoretical lithium-sulfur battery was estimated with the assumption of an electrolyte/sulfur ratio of 2.7 mu L/mg. This was calculated upon 100% of the pore volume in the S/KB-CMC + SBR on Al foam cathodes and polyolefin separator, along with the inclusion of the weights of the tabs for the current lead and pouch film packaging in the case of a seven-layer pouch-type battery. With this calculation, it was determined that the creation of a lithium-sulfur battery with an energy density of greater than 200 Wh/kg is plausible. (C) The Author(s) 2016. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. All rights reserved.

To enlarge the areal capacity of Si-O-C composites as an anode for high energy Li secondary batteries, 3D-structured carbon paper is used as a current collector for electrodeposition of Si-O-C composites. For higher surface affinity between organic solvents with carbon paper, surface treatment of carbon paper is carried out using a sulfuric acid-hydrogen peroxide mixture (SPM) solution. The higher deposited Si amounts and areal capacity are obtained by SPM treatment of carbon paper due to its enhanced surface affinity between carbon paper and electrolytes during Si-O-C electrodeposition. In addition, two kinds of organic solvents, propylene carbonate (PC) and ethylene carbonate/diethyl carbonate (EC/DEC), are employed to investigate their suitability for the electrodeposition of Si-O-C composites. As a result, it is confirmed that the Si-O-C composites synthesized by EC/DEC solvents show more stable cycle abilities than in the case of using PC solvents at a high charge current density of 1.0 mA cm(-2). This is due to the exfoliation of carbon paper by PC, resulting in fast capacity fading during charge/discharge cycle. Nevertheless, it is confirmed that the use of carbon paper as a substrate for Si-O-C electrodeposition is an effective way to increase deposited Si amounts and discharge areal capacity. (C) 2017 The Electrochemical Society. All rights reserved.

Lithium nitrate (LiNO3) is a potential option for the lithium salt in lithium-oxygen (Li-O-2) batteries because it reduces the charging overpotential on carbon-based cathodes and protects the lithium metal anode from side reactions. However, the cycling stability of an electrolyte containing LiNO3 in the presence of cathode catalysts has not yet been studied. In this paper, we report an improvement in the cycling performance of sigma-MnO2 cathodes in Li-O-2 batteries using LiNO3 in comparison with that of batteries using lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) in DMSO- based electrolytes. A > 50% improvement in cycling performance is obtained from the electrolyte with LiNO3 versus that with LiTFSI. While the charge-discharge voltage profiles of the two electrolytes are identical to each other, the electrolyte containing LiNO3 produces less side products such as C-F group compounds, Li2SO3, and Li2SO4 on the cathode surface. This may be due to the electrochemically stable behavior of LiNO3 and the preventive effect of NO3- on solvent decomposition, which stabilizes reactive species of superoxide radicals in the electrolyte. (C) 2017 The Electrochemical Society. All rights reserved.

In this study, we report the preparation of carbon nanotubes (CNTs) anchor layer on a Cu substrate (CNTs/Cu) by using electrophoretic deposition technique. The CNTs anchor layer increases adhesion strength between Si-O-C composites and Cu substrate, as a result, it is possible to improve deposited Si amounts and areal capacity. The electrodeposited Si-O-C composites on CNTs/Cu (Si-O-C/CNTs/Cu) show homogenously coated surface morphology without cracks even large passing charge for electrodeposition of 15 C cm(-2), resulting in 0.21 mg cm(-2) of deposited Si amounts. On the other hand, Si-O-C composites deposited on as-received Cu substrate (Si-O-C/Cu) begin to peel off from substrate at 8 C cm(-2) of passing charge, resulting in 0.13 mg cm(-2) of deposited Si amounts, and decrease down to 0.10 mg cm(-2) at 15 C cm(-2) of passing charge. As a results, the improved Si amounts deposited on CNTs/Cu substrate achieve higher areal capacity, delivering 0.24 mA h cm(-2), which attains increase in 84.6% in comparison to Si-O-C/Cu, which has areal capacity of 0.13 mA g cm(-2) at 8 C cm(-2) of passing charge. Moreover, the Si-O-C/CNTs/Cu shows improved anode performances including discharge capacity and C-rate performance of the Si-O-C composites than Si-O-C/Cu without CNTs anchor layer. (C) 2016 Elsevier B.V. All rights reserved.

To evaluate the efficiency with which intra-and extracellular magnetite nanoparticles (MNPs) induce cell death under an alternating magnetic field (AMF), we comparatively investigated two systems consisting of MCF-7 human breast cancer cells and MNPs: one is a "simply-added" system, which is essentially a simple mixture of cells and extracellular MNPs, and the other is a "pre-cultivated" system that contains both intra-and extracellular MNPs. We also evaluated the effect of heating by thermostatic water bath (WB) on cell death in both systems. The degree of cell death was greater under heating with MNPs subjected to AMF than in the WB-heating in both systems. At higher doses of MNPs, the degree of cell death was greater in the "pre-cultivated" system than in the "simply-added" system using both heating methods. The cellular uptake of MNPs induced slight cell damage and caused a high degree of cell death at higher temperatures. A significant decrease in cell viability was observed in the presence of internalized MNPs under the AMF and was suggested to be a result of the combined effect of intracellular heating and cellular damage by MNPs.

The poor electrical conductivity of Si-based anode materials is a critical challenge for the development of high-performance Li secondary batteries. We propose a new approach for enhancing the electrical conductivity of an electrodeposited Si-O-C composite anode via self-incorporation of nano Cu metal (n-Cu) using a facile and inexpensive electrochemical synthetic method. The Si-O-C composite with n-Cu (Cu/Si-O-C composite) shows stable cycle performance with a fairly high specific capacity. Since Cu precursor ions for the electrodeposition of n-Cu are directly dissolved from a Cu substrate used as the current collector for the anode, electrical conducting additives that causes increase in the weight and volume of the electrode are not unnecessarily supplemented. In the synthesis process, the n-Cu metal and Si-O-C composite are electrodeposited simultaneously. The n-Cu/Si-O-C composite anode results in improved electrochemical performance, including enhancement of areal and specific capacity; coulombic efficiency; and rate capability. Electrochemical impedance spectroscopy suggests that such improvements in performance are due to the enhanced electrical conductivity resulting from the conductive network of the incorporated n-Cu. Moreover, the electrical conductive properties of the incorporated n-Cu suppress electrochemical degradation of the n-Cu/Si-O-C composite anode. (C) 2016 Elsevier Ltd. All rights reserved.

Correction for 'Stimuli-responsive magnetic nanoparticles for tumor-targeted bimodal imaging and photodynamic/hyperthermia combination therapy' by Kyoung Sub Kim, et al., Nanoscale, 2016, DOI: 10.1039/c6nr02273a.

A robust and applicable strategy of signal amplification for field effect transistor (FET) biosensor is of scientifically and technologically importance to detect wide range of target molecules, particularly for the molecules of low charge density, and to configure highly sensitive analysis. In this communication, we demonstrate a simple technique to modify the net charge of target protein based on the concept of protein conjugation for the detection of prion, which is infectious and transmissible protein in neurodegenerative disorders. The increases of prion net charge after chemical modification generate signal amplification and have remarkably enhanced the sensitivity of FET biosensor below than femtomolar (fM) level. Thus, we suggest that such strategy is promising technique for achieving a highly sensitive detection at very low concentration that is useful for early determination of protein biomarkers. (C) 2016 Elsevier B.V. All rights reserved.

Despite magnetic nanoparticles having shown great potential in cancer treatment, tremendous challenges related to diagnostic sensitivity and treatment efficacy for clinical application remain. Herein, we designed optimized multifunctional magnetite nanoparticles (AHP@MNPs), composed of Fe3O4 nanoparticles and photosensitizer conjugated hyaluronic acid (AHP), to achieve enhanced tumor diagnosis and therapy. Fe3O4 nanoparticles (MNPs) were synthesized by a facile hydrolysis method. MNPs have higher biocompatibility, controllable particle sizes, and desirable magnetic properties. The fabricated AHP@MNPs have enhanced water solubility (average size: 108.13 ± 1.08 nm), heat generation properties, and singlet oxygen generation properties upon magnetic and laser irradiation. The AHP@MNPs can target tumors via CD44 receptor-mediated endocytosis, which have enhanced tumor therapeutic effects through photodynamic/hyperthermia-combined treatment without any drugs. We successfully detected tumors implanted in mice via magnetic resonance imaging and optical imaging. Furthermore, we demonstrated the photodynamic/hyperthermia-combined therapeutic efficacy of AHP@MNPs with synergistically enhanced efficacy against cancer.

The electrodeposition-annealing route to fabricating thin film of the promising photocatalyst material anatase-titanium dioxide (anatase-TiO2) has been studied. The sample was deposited with a solution of N,N-dimethylformamide containing titanium compound by controlled-potential technique. SEM image showed the annealed sample at 600 degrees C for 1 h under air provided a continuous film with a thickness of ca. 350 nm. In this sample, X-ray photoelectron spectrumcorresponding to the Ti 2p peak assigned to a chemical bond of TiO2 and X-ray diffraction peaks assigned to the anatase phase were observed, respectively. Electrochemical oxidation in sodium sulfate solution on this annealed film was enhanced in the presence of UV light radiation. These results confirm the successful synthesis of photocatalytic anatase-TiO2 film by the electrodeposition and annealing process. (C) 2016 Elsevier B.V. All rights reserved.

Stable charge-discharge cycling behavior for a lithium metal anode in a dimethylsulfoxide (DMSO)-based electrolyte is strongly desired of lithium-oxygen batteries, because the Li anode is rapidly exhausted as a result of side reactions during cycling in the DMSO solution. Herein, we report a novel electrolyte design for enhancing the cycling performance of Li anodes by using a highly concentrated DMSO-based electrolyte with a specific Li salt. Lithium nitrate (LiNO3), which forms an inorganic compound (Li2O) instead of a soluble product (Li2S) on a lithium surface, exhibits a >20% higher coulombic efficiency than lithium bis(trifluoromethanesulfonyl)imide, lithium bis(fluorosulfonyl)imide, and lithium perchlorate, regardless of the loading current density. Moreover, the stable cycling of Li anodes in DMSO-based electrolytes depends critically on the salt concentration. The highly concentrated electrolyte 4.0 M LiNO3/DMSO displays enhanced and stable cycling performance comparable to that of carbonate -based electrolytes, which had not previously been achieved. We suppose this enhancement is due to the absence of free DMSO solvent in the electrolyte and the promotion of the desolvation of Li ions on the solid electrolyte interphase surface, both being consequences of the unique structure of the electrolyte. (C) 2015 Elsevier B.V. All rights reserved.

The lifetimes of ionic vacancies created in ferricyanide-ferrocyanide redox reaction have been first measured by means of cyclotron magnetohydrodynamic electrode, which is composed of coaxial cylinders partly exposed as electrodes and placed vertically in an electrolytic solution under a vertical magnetic field, so that induced Lorentz force makes ionic vacancies circulate together with the solution along the circumferences. At low magnetic fields, due to low velocities, ionic vacancies once created become extinct on the way of returning, whereas at high magnetic fields, in enhanced velocities, they can come back to their initial birthplaces. Detecting the difference between these two states, we can measure the lifetime of ionic vacancy. As a result, the lifetimes of ionic vacancies created in the oxidation and reduction are the same, and the intrinsic lifetime is 1.25 s, and the formation time of nanobubble from the collision of ionic vacancies is 6.5 ms.

Electrochemical impedance spectroscopy (EIS) using an equivalent circuit is a powerful tool in the diagnosis of lithium-ion batteries (LIBs). However, LIBs have been increasingly used in applications requiring power higher than that used for conventional LIBs for portable electric devices. Considering this demand for LIBs, the ionic resistances in the electrodes, which raise a reaction distribution under high-power operation, are important. This consequently means EIS analysis should include ionic resistances in the electrodes in equivalent circuits. Additionally, the impedance response of LIBs are too complicated to be analyzed in detail because the impedance response consists of overlapping elemental processes such as chemical reactions and ion migration. This paper therefore presents an analysis of impedance responses, which are independently obtained by a micro reference electrode, by using a transmission line model (TLM) that possesses the ability to count the ionic resistances in the electrodes. Similar to the conventional Randles equivalent circuit, the equivalent circuit with TLM could fit the impedance responses simulated by the equivalent circuit with measured responses. This paper discusses the potential of EIS using an equivalent circuit coupled with a TLM for diagnosis of LIBs in power applications. (C) The Author(s) 2015 Published by ECS. All rights reserved.

To provide a bit-patterned perpendicular magnetic recording medium consisting of an array of FePt magnetic nanoparticles, the effect of the total dispersant concentrations of oleylamine and oleic acid in a FePt-nanoparticle/toluene coating solution on a self-assembled nanoparticle array with a long-range periodicity on a flat SiO2/Si substrate and two patterned substrates, respectively, was examined. At a surfactant concentration greater than 0.8 vol%, FePt nanoparticles with an average size of 4.4 nm were arrayed in a two-dimensional and hexagonal-close-packed ordered array with 8.3-nm pitches on the flat surface. Self-assembled nanoparticles were arrayed on the bottom surface of the patterned trench, the array exhibited a hexagonal-close-packed structure. Furthermore the line defects in the arrays are caused by the waviness of the trench walls, and the surface roughness. (C) 2016 The Electrochemical Society. All rights reserved.

A novel polypyrrole (PPy) film was investigated to determine the optimal conditions for operation in a Li/S battery. The PPy film was prepared by oxidative electropolymerization to improve the Li/S battery performance, as reported in our previous paper. In such a system, the PPy film was coated directly on the S/Ketjenblack cathode to solve the problem of polysulfide dissolution. The optimum PPy film preparation conditions to prevent polysulfide dissolution and to promote Li+ permeability were determined by varying the PPy polymerization bath composition and polymerization potential. As a result, the inclusion of 1.0 M lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) in the polymerization bath (0.1 M pyrrole in 1-methyl-1-butylpyrrolidinium bis(trifluoromethanesulfonyl) imide) was found to be the most important factor for producing a PPy film with a high Li+ transport number (t(Li+) approximate to 1). A polymerization potential of 4.5 V versus Li/Li+ was shown to be optimum for the promotion of Li+ permeability. The mechanism by which the PPy film prevents polysulfide dissolution and increases Li+ permeability is discussed by analyzing the SEM, CV, XPS, and C-13 solid-state NMR data. (C) The Author(s) 2016. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/),which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. All rights reserved.

Static degradation of LiCoO2 cathodes is a problem that hinders accurate analysis using our developed separable symmetric cell. Therefore, in this study we investigate the static degradation of LiCoO2 cathodes in separable symmetric cells by electrochemical impedance spectroscopy (EIS) and inductively coupled plasma analyses. EIS measurements of LiCoO2 cathodes are conducted in various electrolytes, with different anions and with or without HF and/or H2O. This allows us to determine the static degradation of LiCoO2 cathodes relative to their increase of charge transfer resistance. The increase of the charge transfer resistance of the LiCoO2 cathodes is attributed to cobalt dissolution from the active material of LiCoO2. Cobalt dissolution from LiCoO2 is revealed to occur even at low potential in the presence of HF, which is generated from LiPF6 and H2O. The results indicate that avoidance of HF generation is important for the analysis of lithium-ion battery electrodes by using the separable cell. These findings reveal the condition to achieve accurate analysis by EIS using the separable cell.

A biosensing system is commercialized based on a concept of physiological balance for healthcare. The addition of low-cost biochemical sensors to the sensing system would help with scientific prescriptions based on contemporary medicine. As a candidate for a low-cost and robust chemical sensor platform, the ion-sensitive field-effect transistor (ISFET) has long been examined. After reviewing past ISFET research, our two approaches for new business trials are discussed. One approach is based on the progressiveness of technology that relies on a public finance with existing big companies. Another approach is a lean startup based on a customer development model for entrepreneurs.

Novel three-dimensional hierarchical heterostructures composed of two-dimensional SnS2 nanoflakes and zero-dimensional SnO2 nanoparticles were fabricated via a one-step hydrothermal method. Size of the heterostructures was ca. 2 mu m in diameter, and individual SnS2 nanoflakes with thickness of ca. 150 nm were connected to central core of the heterostructures. The SnO2 nanoparticles in a diameter of ca. 5 nm uniformly covered entire surface of the SnS2 nanoflakes. Moreover, both of these structures were highly crystalline. Meanwhile, amorphous carbon was formed within the heterostructures. The SnS2/SnO2/C hierarchical heterostructures had a high initial specific reversible capacity of 1065.7 mAh g(-1), stable cycling stability of 638 mAh g(-1) after 30 cycles, and superior rate capability of 550.8 mAh g(-1) at 1C rate. These SnS2/SnO2/C hierarchical heterostructures showed better performance than individual SnS2 and SnO2 nanomaterials, and the performance was even higher than the graphene-SnS2 and graphene-SnO2 nanohybrid materials. This is attributed to a synergistic effect of high surface area, which is provided by the unique SnS2 internal nanoflake layered structures decorated with ultra-fine SnO2 nanoparticles, and an effective beneficial buffer matrix to accommodate the large volume change upon cycling, which is caused by the side-products such as Li2S or Li2O. The SnS2 nanoflake was deduced to play a similar role as graphene material, since both possess 2D conducting layer structures. The uniform carbon dispersion within the structures also stabilizes the structures and improves electrical conductivity of the hierarchical heterostructures. (C) 2015 Elsevier Ltd. All rights reserved.

To compare heat generation under an AC magnetic field for inducing cancer cell death, CoFe2O4 and Fe3O4 nanoparticles with a diameter of similar to 10 nm were synthesized by hydrolysis in an aqueous solution containing the metal chlorides iron(III) chloride and cobalt(II) or iron(II) chloride, with spermine or N,N'-bis(3-aminopropyl)butane-1,4-diamine, as a base and a protective reagent. Both CoFe2O4 and Fe3O4 nanoparticles were incorporated into human breast cancer MCF-7 cells; the nanoparticles exhibited little toxicity on the cells. When the cells containing nanoparticles were subjected to an AC magnetic field, MCF-7 cell death was induced by heat generated from similar to 10-nm CoFe2O4 nanoparticles but not from similar to 10-nm Fe3O4 nanoparticles. An increase in coercivity derived from the substitution of Fe2+ with Co2+ facilitated the ability of the nanoparticles to induce cell death in human breast cancer cells under an AC magnetic field. (C) 2015 Elsevier Ltd. All rights reserved.

A facile and scalable method is proposed to prepare microscale Li2S-C composite from Li2SO4 through carbon-thermal reduction, followed by a carbon coating process. Multi-solvent recrystallization was utilized to reduce the particle size of Li2SO4 to 2 mu m. This fine-grain Li2SO4 helps to shorten the particle size of reduction product from 10 mu mto 3 mu m. Using fine Li2SO4 also brings the benefit of greatly reducing the over potential during the initial charge process and increasing the kinetics for Li2S materials. Finally, the microscale Li2S-C composite prepared from fine Li2SO4 enables a stable capacity of 350 mAh g(-1) at 0.2 C, higher than that obtained using a cathode prepared from commercial Li2SO4. (C) 2015 Elsevier Ltd. All rights reserved.

We have developed a field effect transistor (FET) sensor to sensitively detect copper ions (Cu(2+)) in a human serum (HS) sample for promising health-care diagnosis. By utilizing a Cu(2+)-binding prion protein that was immobilized on the FET gate surface, such an FET sensor can provide a simple, label free and highly selective performance, even in HS samples. We demonstrated the sensitivity of the sensor at the nanomolar level, 0-100 nM, which is very useful for the detection range of Cu(2+) deficiency in practical applications.

The effect of the solid electrolyte interphase (SEI) on a Li anode on the charge-discharge cycling performance in 1 M LiTFSI/dimethylsulfoxide electrolyte solution is examined by using charge-discharge cycling. The chemical structure of the surface and interior of the SEI strongly affects the cycling performance of the anode. The observed coulombic efficiency is low (<45%) when organic compounds such as lithium alkyl carbonates and polycarbonate form predominantly on the surface and interior. However, when inorganic compounds such as Li2CO3, Li2O, and LiF form instead, the coulombic efficiency increases to >85%. This enhanced efficiency remains constant regardless of the O-2 content and despite <1000 ppm concentration of the contaminant H2O in the electrolyte. Thus, the lithium surface should be protected by inorganic compounds prior to cycling to prevent it from undergoing side reactions with the electrolyte during cycling in the electrolyte. (C) 2015 Elsevier B.V. All rights reserved.

To realize electrochemical impedance spectroscopy (EIS) using a simple measurement system, application of a square potential/current waveform to the input signals of EIS was investigated. The impedance of a simple redox reaction of [Fe(CN)(6)](4-)/[Fe(CN)(6)](3-) solution was measured by the potentio-EIS using a square waveform as the input signal, which was generated by a potentiostat system without a frequency response analyzer (FRA). A steady impedance response in the frequency range of 40 Hz-3.5 kHz was obtained, and the impedance was obtained by the potentiostat system with an FRA. The errors-the differences between the impedance measured by EIS with a square potential waveform and that of conventional EIS-were sufficiently low to allow impedance analysis. The impedance of a lithium-ion battery (LIB) was measured by galvano-EIS using a square waveform input signal generated by a power controller. A steady impedance response in the frequency range of 5 Hz-2.5 kHz was obtained, and the errors were sufficiently low to allow impedance analysis. It was demonstrated that both square potential-EIS (SP-EIS) and square current-EIS (SC-EIS) have great potential as simple systems for measuring impedance. Moreover, it was demonstrated that SC-EIS has potential as a simple measurement system for analyzing the state of an LIB. Thus, the potential of the SP/SC-EIS methodology was confirmed for electrochemical systems. (C) 2015 Published by Elsevier Ltd.

Nanoparticle uptake and cell death following addition of magnetite nanoparticles (MNPs) with a diameter of ∼10 nm were evaluated in three histological types of human mesothelioma cells, NCI-H28 (epithelioid), NCI-H2052 (sarcomatoid), and MSTO-211H (biphasic) cells, and human breast cancer MCF-7 cells. Dose-dependent cell death was observed in MSTO-211H cells but not in MCF-7 cells, although cellular uptake of MNPs was observed in both cell types. Mesothelioma NCI-H28 and NCI-H2052 cells showed behavior more similar to that of breast cancer MCF-7 cells than that of mesothelioma MSTO-211H cells. DNA fragmentation and microarray analyses suggested that MNPs induced transforming growth factor β2 related apoptosis in MSTO-211H cells. On the other hand, the viability of human mesothelioma cells containing MNPs with a diameter of ∼40 nm was investigated after exposure to an alternating magnetic field. Temperature increase under the alternating magnetic field and high rates of cell death were observed in all three histological types of human mesothelioma.

We report micrometre-thick porous Si-Cu anodes that are rapidly co-deposited on Cu current collectors in 1 mm. This rapid deposition is realized by heating Si and Cu powders to similar to 2000 degrees C and elevating their vapour pressures, while the porous and amorphous anode structure is realized by keeping the substrates at 100 degrees C. The films spontaneously form a 2-4.5-mu m-thick composition gradient that changes from a Cu-rich region at the bottom to a Si-rich region at the top of the film, because of the higher vapour pressure for Cu than Si. A small addition of 5 wt% Cu to the Si source enhances the cycle performance of the film remarkably in a half-cell test, yielding a gravimetric capacity of 1250 mAh g(film)(-1), a volumetric capacity of 1956 mAh cm(film)(-3), and an areal capacity of 0.96 mAh cm(anode)(-2) at the 100th cycle. However, excess addition of Cu causes partial Si crystallization in the films, which results in poorer cycle performance. While further improvement is needed, this rapid vapour deposition method yields Si-Cu films with compositional gradients on Cu current collectors in 1 min using inexpensive and safe Si and Cu powder sources, and is attractive for practical Si-based anode fabrication. (C) 2015 Elsevier B.V. All rights reserved.

Detection of tumor markers is important for cancer diagnosis. Field effect transistor (FET) has been recognized as a powerful technique for label-free, sensitive, real-time, and multifunctional biosensing. Here, we developed FET biosensors that allow the label-free detection of cytokeratin fragment 21-1 (CYFRA 21-1) and neuron-specific enolase (NSE), useful tumor markers for lung cancer type differentiation. It was found that the FET biosensor was capable of quantitatively detecting these tumor markers in both phosphate-buffered saline and human serum. Additionally, we developed a multianalyte FET biosensor for the selective multiplexed detection of CYFRA 21-1 and NSE at the same time, by integrating two antibody types on the same chip, providing a step towards the realization of sensor arrays. The multianalyte FET biosensor, as described herein, will help for lung cancer differential diagnosis with advantages of simple and rapid detection procedures, low sample consumption, and low cost. (C) 2015 Elsevier B.V. All rights reserved.

Simple and accurate detection of prion proteins in biological samples is of utmost importance in recent years. In this study, we developed a label-free electrical detection-based field effect transistor (FET) biosensor using thiamine as a probe molecule for a non-invasive and specific test of human prion protein detection. We found that thiamine-immobilized FETs can be used to observe the prion protein oligomer, and might be a significant test for the early diagnosis of prion-related diseases. The thiamine-immobilized FET was also demonstrated for the detection of prion proteins in blood serum without any complex pre-treatments. Furthermore, we designed a dual-ligand binding approach by the addition of metal ions as a second ligand to bind with the adsorbed prion protein on the thiamine-immobilized surface. When the prion attached to metal ions, the additional positive charge was induced on the gate surface of the FET. This approach was capable of amplifying the magnitude of the FET response and of enhancing the sensitivity of the FET biosensor. Detection of prion proteins has achieved the required concentration for clinical diagnosis in blood serum, which is less than 2 nM. In summary, this FET biosensor was successfully applied to prion detection and proved useful as a simple, fast, sensitive and low-cost method towards a mass-scale and routine blood screening-based test.

The electrodeposited Sn-O-C composite anode cycling with LiClO4 delivered stable cycle performances showing discharge capacity of 473 mA h g Risri with 95% of coulombic efficiency at 100th cycle. However, the anode showed poor cycle performances with LiPF6 delivering discharge capacity of 69 mA h g(-1) of sn at 100th cycle with 70% of coulombic efficiency. Electrochemical investigation performed by cyclic voltammetry and differential capacity plots revealed that the Sn-O-C composite cycling with LiPF86 suffered from retarded phase transition reaction between Li and Sn during charge/discharge process. X-ray photoelectron spectroscopy declared the existence of fluorinated-Sn and LiF. Moreover, energy dispersive X-ray spectroscopy found increase in their amount with repeated cycles. The morphologies of the Sn-O-C composite cycled with LiPF6 showed aggregated particles containing the chemical state of fluorinated-Sn and LiF on its surface. Furthermore, the significant pulverization and aggregation of the active material were observed from the Sn-O-C composite cycled by LiPF6 rather than that of LiClO4, which was probably promoted by the generated HF strongly corroding metallic component. (C) 2014 Elsevier B.V. All rights reserved.

Lithium-ion batteries (LIBs) are generally constructed by lithium-including positive electrode materials, such as LiCoO2, and lithium-free negative electrode materials, such as graphite. Recently, lithium-free positive electrode materials, such as sulfur, are gathering great attention from their very high capacities, thereby significantly increasing the energy density of LIBs. Though the lithium-free materials need to be combined with lithium-containing negative electrode materials, the latter has not been well developed yet. In this work, the feasibility of Li-rich Li-Si alloy is examined as a lithium-containing negative electrode material. Li-rich Li-Si alloy is prepared by the melt-solidification of Li and Si metals with the composition of Li21Si5. By repeating delithiation/lithiation cycles, Li-Si particles turn into porous structure, whereas the original particle size remains unchanged. Since Li-Si is free from severe constriction/expansion upon delithiation/lithiation, it shows much better cyclability than Si. The feasibility of the Li-Si alloy is further examined by constructing a full-cell together with a lithium-free positive electrode. Though Li-Si alloy is too active to be mixed with binder polymers, the coating with carbon-black powder by physical mixing is found to prevent the undesirable reactions of Li-Si alloy with binder polymers, and thus enables the construction of a more practical electrochemical cell.

In order to solve the problem of polysulfide dissolution into the electrolyte on sulfur-based cathodes, we propose a novel method of modifying the S cathode by coating it with a polypyrrole (PPy) film, which is prepared by oxidative electropolymerization using a solution consisting of, 1-methyl-1-butylpyrrolidinium bis(trifluoromethanesulfonyl)imide, lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and pyrrole. The PPy film demonstrates a high Li+ transport number. The film also exhibits a superior ability to inhibit polysulfide dissolution into the electrolyte during the charge discharge cycles. Furthermore, the charge discharge properties of the coated cathode is evaluated using an electrolyte consisting of 1.0 M LiTFSI in a mixture of 1,2-dimethoxyethane (DME) and 1,3-dioxolane (DOL), which is known to easily dissolve polysulfides. Because of the surface modification with the PPy film, the cathode exhibits excellent specific capacities of 823 and 354 mAh g(-1) at C-rates of 0.1 and 1.0 C, respectively, with high coulombic efficiency. Thus, the strategy of coating the S cathode with PPy is successful in inhibiting the polysulfides dissolution even in electrolytes known to easily dissolve polysulfides, besides allowing high C-rate operation. Further, the modification of the S cathode allows the selection of a suitable electrolyte based on the anode, rather than being limited by the cathode. (C) 2014 Elsevier B.V. All rights reserved.

Electroless deposition (ELD) is a well-known method for preparing thin films of metals and their alloys. It is a highly selective method allowing additive patterning of isolated and embedded structures on insulating substrates, e.g. glass, plastic or ceramic. It is a relatively low temperature (less than the boiling point of the electrolyte) and low cost process compared to other physical and chemical vapor deposition methods. ELD features uniform and normally conformal deposition (additives may affect its conformality) with low defect density and some unique material properties. In the last 30 years electroless plating of metals (e.g. copper, gold, nickel, cobalt, palladium, iron, silver, etc.) and their alloys, was demonstrated for micro system applications: microelectronics, micro electro mechanics, micro electro optics and microfluidics, micro fuel cells, micro batteries etc. Electroless plating was also demonstrated on nano structures, both artificial and natural. In this paper we present a short tribute to the recent advances in electroless plating in the last 30 years. Those advances and innovations are due to the work of many scientists and engineers on a time span started in the 19th century. The progress in electroless plating followed the need and the trend for better metallization technologies for complex structures with critical dimensions that had been shrinking continuously in the last few decades. (C) 2014 Elsevier B.V. All rights reserved.

The electrode surfaces of degraded lithium-ion batteries (LIB) were analyzed by liquid chromatography-quadrupole time of flight mass spectrometry (LC-QTOF/MS). The solid-electrolyte interphase (SET) layer influences the performance of LIBs. Therefore, we conducted a study aimed at clarifying the deterioration mechanism of LIBs by examining the components in the SET before and after degradation due to cycling. We believe that the change in the mass transfer characteristics at the electrode interface influenced by SET deterioration can be clarified via Lc-QTOF/MS, which would allow elucidation of the deterioration mechanism. The analysis results showed that the degradation products contain multiple components, including polymers of carbonate compounds and phosphate esters, which are formed via electrochemical and chemical reactions, resulting in remarkably reduced capacity. The results suggest that LC-QTOF/MS is a valuable technique for the degradation analysis of LIBs. (C) The Author(s) 2015. Published by ECS. All rights reserved.

Electrochemical impedance spectroscopy (EIS) can be utilized to characterize battery features, because it allows the dynamics of each elemental process of the battery reaction to be sensitively and separately determined without destruction of the cell. In addition, EIS is expected to be utilized for premonitory diagnosis of onboard batteries in electric vehicles. Here; an overview of the recent diagnosis technologies for determining the health of commercial lithium-ion batteries (LIB) using EIS is provided. We describe equivalent circuit design techniques while explaining and investigating physical and chemical phenomena for a wide range of measured impedance spectra, which are obtained using commercial LIBs.. Attention is then focused on separation of the frequency responses of each electrode with or without a reference electrode, symmetric cell, and temperature control. Additionally, a square-current EIS (SC-EIS) technique, which we have proposed, is introduced for monitoring of large-scale LIB systems as a promising future technique. (C) 2015 The Electrochemical Society. All rights reserved.

A novel 3D porous Si-O-C/Ni thick film anode is successfully prepared by electrodeposition of porous Ni on Cu substrate and galvanostatical electrodeposition of Si-O-C composite on porous Ni substrate. The 3D porous Si-O-C/Ni thick film is electrochemically activated at a current density of 50 mu A cm(-2) for the first cycle and 200 mu A cm(-2) (0.5 C) for the subsequent cycles, it displays superior electrochemical performance with discharge capacity of 706.3 mAh g(-1) of Si after 100 cycles. The properties of this thick film is analyzed by field emission scanning electron microscopy (FESEM) and scanning transmission electron microscopy with energy dispersive X-ray analyzer (STEM-EDX). The results show that Si-O-C composite not only covers the surface area of porous Ni but also attaches to the highly porous dendritic walls, along with the porous structure of Ni which provides proper accommodation for the volume change of silicon during the lithiation/delithiation processes, are believed to result in the high capacity and excellent cyclability. (C) 2014 Elsevier B.V. All rights reserved.

Nitrogen-doped/undoped thermally reduced graphene oxide (N-rGO) decorated with CoMn2O4 (CMO) nanoparticles were synthesized using a simple one-step hydrothermal method. The activity and stability of this hybrid catalyst were evaluated by preparing air electrodes with both primary and rechargeable zinc-air batteries that consume ambient air. Further, we investigated the relationship between the physical properties and the electrochemical results for hybrid electrodes at various cycles using X-ray diffraction, scanning electron microscopy, galvanodynamic charge-discharging and electrochemical impedance spectroscopy. The structural, morphological and electrocatalytic performances confirm that CMO/N-rGO is a promising material for safe, reliable, and long-lasting air cathodes for both primary and rechargeable zinc-air batteries that consume air under ambient condition.

The effects of a small amount of H2O with and without CO2 in an electrolyte of I M LiPF6/ethylene carbonate and diethyl carbonate on the cycling life of a Li metal anode is investigated in this paper using charge discharge cycling. A low cycling performance, which is less than 55%, is observed with the electrolyte with trace H2O but without CO2; however, when the trace H2O is accompanied by CO2, performance drastically improves and coulombic efficiency reaches a maximum of 88.9%. In the presence of CO2, the cycling performance is found to be strongly affected by the H2O content in the electrolyte, and increases with an increase in H2O content of up to 35 ppm. From an X-ray photoelectron spectroscopy analysis, trace H2O is found to affect the compounds of the solid electrolyte interphase (SEI) on the lithium surface and produces an Li2CO3 and LW layer on the upper part of the SEI, both known to be good passivation layers for preventing side reactions during charge discharge cycling. (c) 2014 Elsevier B.V. All rights reserved.

Ionic vacancies created in copper electrodeposition have been first observed by converting to microbubbles via. nanobubbles. Since the copper deposition potential was much more positive than hydrogen evolution one, the microbubbles were ascribed not to hydrogen bubbles but to the ionic vacancies. Then, the evolution times of the microbubbles at an overpotential of -300 mV were examined under various magnetic flux densities. (C) The Electrochemical Society of Japan, All rights reserved.

The nitrogen-doped carbon nanocapsules (NCNCs) were explored as catalyst support for oxygen reduction reaction (ORR) in acid electrolyte. The deposition of Pt particles on NCNCs support was characterized using various physico-chemical techniques, such as scanning electron microscope, transmission electron microscope, X-ray diffraction, and X-ray photoelectron spectroscopy. The high resolution transmission electron microscopy reveals that Pt particles are uniformly dispersed onto the NCNCs and particles size of about 2.2 nm was observed. The electrochemical ORR activities of the Pt supported on NCNCs catalysts were studied and compared with a commercial catalyst. Pt/NCNC showed enhanced ORR activity and better stability than a commercial Pt/C catalyst. The enhanced performance of Pt supported NCNCs can be attributed to the better dispersion and utilization of Pt nanoparticles. (C) 2014 Elsevier Ltd. All rights reserved.

In this paper, we report a lithium-ion battery employing a lithium sulfide cathode and a silicon-based anode. The high capacity of the silicon anode and the high efficiency and cycling rate of the lithium sulfide cathode allowed optimal full cell balance. We show in fact that the battery operates with a very stable capacity of about 280 mAh g(-1) at an average voltage of 1.4 V. To the best of our knowledge, this battery is one of the rare examples of lithium-metal-free sulfur battery. Considering the high theoretical capacity of the employed electrodes, we believe that the battery here reported may be of potential interest as high-energy, safe, and low-cost power source for electric vehicles.

The impedance behaviors of Si-O-C composite film electrodeposited on Cu microcones-arrayed current collector have been investigated to understand the electrochemical process kinetics that influences the cycling performance when used as a highly-durable anode in a lithium battery. The impedance was measured by using impedance spectroscopy in equilibrium conditions at various depths of discharge and during several hundred charge-discharge cycles. The measured impedance was interpreted with an equivalent circuit composed of solid electrolyte interphase (SEI) film, charge transfer and solid state diffusion. The impedance analysis shows that the change of charge transfer resistance is the main contribution to the total resistance Change during discharge, but an abrupt augmentation of diffusive resistance at high depth of discharge is also observed which cannot be explained very well by the presented model. The impedance evolution of this electrode during charge-discharge cycles suggests that the slow growth of the SEI film as well as the increase of the electrode density are responsible for the capacity fading after long term cycling. (C) 2014 Elsevier B.V. All rights reserved.

Symmetric cells were prepared with a newly designed separable cell module, which enabled ca. 70 mm by 70 mm electrode sheets to be used for a pouch type 5 Ah class Li-ion battery (LIB). Impedance analysis of the LIB as a full cell state was successfully performed with electrochemical parameters obtained by an impedance analysis of symmetric cells of anodes and cathodes obtained from the operated Li-ion batteries. While the charge transfer resistance of the cathode was found to increase after reassembling the cells symmetrically, other electrochemical parameters were found not to change when comparing the values obtained for full cells with symmetric cells. Eelectrodes degraded by charge/discharge cycling of the battery were also investigated, and the parameter change caused by the degradation was confirmed. (C) 2014 Elsevier Ltd. All rights reserved.

A carbon-coated Li2S was prepared through an adsorption and successive annealing process by using poly(vinylpyrrolidone) (PVP) and acetylene black (AB) as carbon source with Li2S powder. The coating layer was composed of amorphous carbon and embedded AB particles. The carbon coating was found to effectively alleviate the dissolution of polysulfide and the discharge capacity at the first 15 cycles was 800 mA h g(-1) with gradual fading afterward.

We propose, as an alternative to conventional spectroscopic assays, a simple method for discriminating fibrous amyloid proteins by using a label-free semiconductor-based biosensor. The highly sensitive assay is expected to be useful for accelerating amyloid related research.

In this paper, we report the effects of chemical treatment of indium tin oxide (ITO) surface on its surface chemistry such as chemical composition and surface roughness and on its usage as an electrode with monolayer modification. Atomic force microscopy, angel-resolved X-ray photoelectron spectroscopy, and Kelvin probe force microscopy have been used to investigate the morphology and the chemical properties of commercial thin ITO films after several treatments commonly used prior to the formation of organic layer on the surface. The amount of spike present on the surface of as-received ITO substrates was significantly reduced by etching with KOH whereas the roughness of ITO increased with HCI etching. We demonstrated that the successive treatment of ITO electrode with HCI and KOH affects the surface characteristics such as roughness and work function, contributing to the potentiometric detection of tiyptophan. (C) 2014 Elsevier B.V. All rights reserved.

Detection of tumor markers is important for cancer diagnosis. Field-effect transistors (FETs) are a promising method for the label-free detection of trace amounts of biomolecules. However, detection of electrically charged proteins using antibody-immobilized FETs is limited by ionic screening by the large probe molecules adsorbed to the transistor gate surface, reducing sensor responsiveness. Here, we investigated the effect of probe molecule size on the detection of a tumor marker, α-fetoprotein (AFP) using a FET biosensor. We demonstrated that the small receptor antigen binding fragment (Fab), immobilized on a sensing surface as small as 2-3 nm, offers a higher degree of sensitivity and a wider concentration range (100 pg/mL-1 μg/mL) for the FET detection of AFP in buffer solution, compared to the whole antibody. Therefore, the use of a small Fab probe molecule instead of a whole antibody is shown to be effective for improving the sensitivity of AFP detection in FET biosensors. Furthermore, we also demonstrated that a Fab-immobilized FET subjected to a blocking treatment, to avoid non-specific interactions, could sensitively and selectively detect AFP in human serum.

We fabricated dye-sensitized solar cells (DSSCs) with synthetic quartz nanoparticle (SQNP)-supported Pt/fluorine doped tin oxide counter electrodes to utilize an adsorptive capacity of synthetic quartz. The amperage of I-3(-) reduction was 1.6 times higher with SQNP than that without SQNP. SQNP also improved the photocurrent density-voltage characteristics and the incident photon to current conversion efficiency spectra in the visible region. These suggest that SQNP enhances the I-3(-) reduction activity on the counter electrode and the electron transfer to the photoanode. The SQNP-supported counter electrode is expected to be useful to raise the efficiency of a DSSC. (C) The Electrochemical Society of Japan, All rights reserved.

Silicon is one of the most promising materials for lithium secondary battery anodes. However, silicon anodes have a critical drawback to their practical application, which is capacity degradation due to pulverization of the active material by the large volume change of silicon during charge-discharge cycles. This paper reviews recent studies on silicon-based anodes that have attempted to overcome this poor cycle durability through structural control such as through thin films, porous structures, core-shell structures, and by alloying with other metals, and by application of proper binders. Among them, binder-free Si-O-C composite films prepared by electrodeposition exhibit outstanding cycle durability. The origin of this excellent durability is discussed in depth from the standpoint of chemical and morphological changes. Consequently, the combination of active materials such as Si and Li2Si2O5 and inactive materials such as L(i)2O, Li2CO3, and organic compounds is suggested to result in outstanding properties as a lithium secondary battery anode.

Sn-O-C composites were electrodeposited using organic carbonate solvents and their electrochemical mechanism was thoroughly investigated to achieve desired anode performances, such as high capacity and cycle durability for lithium secondary batteries. Cyclic voltammetry study clarified the multiple stages of electrochemical mechanism during the Sn-O-C composite deposition process. It was revealed that Sn deposition, decomposition of organic electrolytes, and reaction between Li+ and deposited Sn were consecutively carried out. X-ray photoelectron spectroscopy and field emission scanning electron microscopy were performed to characterize how each stage contributes to the formation of the Sn-O-C composite. The results showed increase in metallic Sn composition and dense coating with fine particle sizes with a higher overpotential stage. Afterward, different Sn-O-C composite anodes were prepared by varying charge quantities passing through each deposition stage and their electrochemical performances as anode materials were investigated. Discharge capacities were obtained from the lowest value of 33 mAh g of Sn-1 to the highest value of 429 mAh g of Sn-1 at the 100th cycle by varying deposition conditions. Consequently, it was suggested that anode performance was significantly influenced by an electrodeposition process consisting of three consecutive stages with different overpotential regions and reactions of Li ion with deposited Sn. (C) 2014 The Electrochemical Society. All rights reserved.

Electrodeposition was conducted from an organic carbonate solvent via the potentiostatic technique through three consecutive steps in order to synthesise Sn-O-C composite, which delivered a discharge capacity of 596 mA h g of Sn-1 after 50 cycles. However, the composite anode suffered from a significantly low initial discharge capacity, delivering a discharge capacity of 79 mA h g of Sn-1 until the 5th cycle. It was deduced that the improbably low initial capacity was induced by the deposition of Li-rich compounds, which were formed by electrolyte decomposition accompanied by the reduction product of supporting electrolyte salts during the electrodeposition process, on the surface layer. In order to improve the poor initial capacity, we modified the chemical composition of the surface layer by means of implementing the agitation of the electrolyte during the deposition process. This gave rise to varying the diffusion-layer thickness during the deposition process due to the enhancement of convection by movement of the electrolyte itself. As a result, we achieved improvement of the initial discharge capacity, delivering 572 mA h g of Sn-1 at the 1st cycle and 586 mA h g of Sn-1 at the 50th cycle. It was revealed that the surface layer was composed of a decomposition product of the organic carbonate solvent. Furthermore, a smaller particle size of the Sn-O-C composite was obtained via electrolyte agitation, giving rise to homogeneous shell formation on the Sn compound core. Herein, we thoroughly examined the influence of varying diffusion-layer thickness during the deposition process on the properties of the Sn-O-C composites from an electrochemical standpoint.

A common understanding of polymer electrolyte fuel cells (PEFCs) is important to promote the development of PEFCs. This understanding is crucial because complicated phenomena such as chemical reactions, ion transport, and gas diffusion occur during the operation of PEFCs. Electrochemical impedance spectroscopy (EIS), which can separate reactions into elementary processes, is a powerful tool for the analysis of PEFCs without requiring disassembly of the cell. In this study, the effect of flooding in the cathode catalyst layer of PEFCs was analyzed by EIS using the transmission line model (TLM) to determine the distribution of catalytic reactions in the primary and secondary pores. The analysis was conducted by varying experimental conditions such as the relative humidity of the gases supplied into the anode and cathode, the flow rate, and the partial pressure of oxygen in the gas mixture supplied to the cathode channel. The EIS analysis suggests that the resistance to the catalytic reaction in the primary pores drastically increased with the current density. The results suggest that the flooding preferentially occurred in the primary pores, resulting in the reduction of active sites by generated water. The EIS method is a powerful tool for developing membrane electrode assemblies (MEAs) with effective porosity and tortuosity for gas diffusion and ionic transportation, and furthermore, it is a useful tool for judging the process of MEA preparation. (C) 2013 Elsevier Ltd. All rights reserved.

First of all, we express our deepest sympathies for the passing of Professor Su-Moon Park. In the present paper, an electrochemical impedance spectroscopy (EIS), which Professor Su-Moon Park also used frequently for the investigation of electroconducting polymer, is introduced as a recent evaluation tool for a commercially available lithium-ion battery (LIB). The paper surveys how to design equivalent circuits while explaining physical and chemical phenomena in the LIB and how to get more accurate impedance spectra with varying the measuring temperatures. Additionally, a square current EIS (SC-EIS) technique, which we have suggested, is introduced for the larger LIB system as a promising technique for the future.

The structure of the highly durable silicon-based anode prepared by electrodeposition was investigated for volume change and chemical structure. With repeated charge-discharge cycles, the volume change resulting from the anode film thickness decreased, and, after 100 cycles, essentially no difference was observed between the charged and discharged states. The buffering effect of the volume change was considered to be achieved by the formation of Li2O, Li2CO3, and lithium silicates such as Li4SiO4, whose existence were supported by STEM, EELS, and XPS analyses. From the structural analyses, the main reactions related to the capacity of the silicon-based anode were considered to be the formation of LixSi and Li2Si2O5. LixSi and Li2Si2O5 can be delithiated into Si and SiO2, respectively. (C) 2013 Elsevier Ltd. All rights reserved.

The Sn-O-C composite anode for the Li secondary battery was synthesized by electrodeposition using an organic carbonate solvent. The composite of Sn with organic/inorganic compounds was prepared by the simultaneous reaction of the reduction of Sn2+ ions and electrolysis of the mixture of ethylene carbonate and propylene carbonate. The galvanostatic potential transients for the electrodeposition of the Sn-O-C composite indicate that multiple steps of reactions corresponding to the electrochemical reduction of the tin precursor and the decomposition of organic solvents are involved. The morphology, crystalline structure and chemical composition of the as-deposited Sn-O-C composite anode were characterized to elucidate the mechanism of the synthesis of the buffering matrix enduring volume expansion.The electrochemical behavior of the Sn-O-C composite anode was investigated by cyclic voltammetry and galvanostatical charge/discharged tests. The discharge capacity of 465 mAh (g of Sn)(-1) was obtained at the 100th cycle showing 80% of the capacity retention after the 100th cycle. The discharge capacity was stable after the 50th cycle, where the phase transformation of the Sn element from Sn to Li0.4Sn at the discharged state was found. (C) 2013 Elsevier B.V. All rights reserved.

Allergy diagnosis, conducted to determine whether a specific syndrome is attributable to allergy, plays a significant role in the overall health examination. In this paper we report that the detection of allergy-associated protein, immunoglobulin E (IgE), was achieved by using field effect transistors (FETs) immobilized with an antigen as a receptor, which is smaller in size than the conventional receptor (antibody). The antigen-immobilized FETs exhibit a higher response to IgE than the antibody-immobilized FETs, suggesting that the smaller receptor not only makes the more effective use of the charge-detectable region for the PET-based detection in terms of Debye length, but also provides more recognition sites for target molecules and greater ability to block nonspecific adsorption of non-related proteins because of the closely-packed immobilized receptors. In addition, the application of the antigen to FET biosensor gives an advantage in the identification of the specific allergen. These results show that the small receptor of antigen is more effective than the antibody in the allergy detection using PET biosensors. (C) 2013 Elsevier Ltd. All rights reserved.

Influenza virus, through cell invasion and propagation with the interaction between hemagglutinin (HA) present on its surface and glycans on the host cell, causes a rapidly spreading infection throughout the world. In the present investigation, we succeeded for the first time in the attomolar-level sensing and discrimination of influenza A viral HA molecules H1 and H5 by using a glycan-immobilized field effect transistor (FET) biosensor. The small ligand glycans immobilized on the FET device, which make effective use of the charge-detectable region for FET-based detection in terms of Debye length, gave an advantage in the highly sensitive detection of the proteins. Two kinds of trisaccharides receptors terminating in sialic acid-α2,6-galactose (6'-sialyllactose) and in sialic acid-α2,3-galactose (3'-sialyllactose) were conjugated directly with the SiO2 surface of FET devices by a simple glycoblotting method using the self-assembled monolayer (SAM) of aminooxy terminated silane-coupling reagent, 3-aminooxypropyltriethoxysilane. Furthermore, it was demonstrated that the FETs with densely immobilized glycans, which possess the high capture ability by achieving the glycoside cluster effect, clearly distinguish HA molecules between their subtypes H1 (human) and H5 (avian) at the attomolar level, while the conventional method based on HA antibodies achieves only picomolar-level detection. Our findings indicate that the glycan-immobilized FET is a promising device to detect various pathogenic bacteria and viruses through glycan-protein interaction found ubiquitously in many infectious diseases.

Hybrids possessing both oligomeric ethylene oxide chains and Ti-O-P networks were prepared from TiCl4 and organodiphosphonic acid [(HO)(2)OP(C2H4O)(3)C2H4PO(OH)(2)] via a nonhydrolytic sol gel process and subsequently treated with a LiClO4 solution. The P/Ti ratio was fixed at 2 and the ethylene oxide unit/Li+ ratio was changed from 5 to 20. Li+ ions are likely to be solvated by ether oxygen atoms. Li+ ion transport in the hybrids with ionic conductivity values in the 10(-5) S cm(-1) range was observed at ambient temperatures.

The impedance of Li-ion battery using a Li4Ti5O12 (LTO) anode for high-power applications was measured at various depths of discharge and temperatures during charge discharge cycles. The measured impedance was interpreted with an equivalent circuit made up of anode and cathode, in which the cathode component was composed of two particle size factors. The values obtained for equivalent circuit elements by modeling were in good agreement with the results measured by other techniques, and indicated that the capacity fade of this Li-ion battery due to cycling is mainly caused by the increase of interfacial resistance and a decrease in the capacity of the LiCoO2 cathode. These results suggest that the cyclability of this LIB was improved by using an LTO anode, and show the validity of the equivalent circuit for interpreting the causes of capacity fade. (C) 2012 Elsevier B.V. All rights reserved.

Electrodeposition methods were developed for the fabrication of Si composite anodes with nickel micro-nanocones hierarchical structure (MHS) current collectors for Li secondary batteries. This unique structured nickel current collector is electrodeposited in a simple process to create a complex high surface area conductive substrate, as well as to enhance the interfacial strength between active materials and substrate during cyclic lithiation/delithiation. The MHS supported Si composite anode demonstrated outstanding Li+ storage properties with reversible capacity over 800 mAh g(-1) (600 mu Ah cm(-2)) after 100th cycle with superior retention of 99.6% per cycle. The improved performance of nickel MHS supported Si thick films indicate the potential for their application as electrode materials for high performance energy storage. 2012 Elsevier B.V. All rights reserved.

From the observation of coalesced microbubbles arising from supersaturated nanobubbles in ferricyanide/ferrocyanide redox reaction, the first evidence of the conversion from ionic vacancies to nanobubbles has been obtained. Since ionic vacancies are created without any electron transfer, the microbubbles are evolved in a different way from ordinal electrochemical gas reactions. © 2013, The Electrochemical Society of Japan. All rights reserved.

Au-Ni-C alloys films electrodeposited by a pulsed current method were investigated to assess the crystalline structure, sheet resistance, and wear resistance, for use as an electronic contact material. In particular, we have analyzed the effects of citric acid concentration and pulse off-time on the mechanical and electrical properties of the electrodeposited Au-Ni-C alloy films. The electrodeposition bath used in this study was composed of K[Au(CN)(2)] and NiSO4 center dot 6H(2)O as precursors, and citric acid as the complexing agent. The film microstructure and composition were controlled by adjusting the interval of pulse off-time and the concentration of citric acid. With the prolongation of the pulse off-time interval, XRD results indicated that the amorphous structure with high Ni and C contents was transformed into a nanocrystalline structure, followed by the formation of crystals with small Ni and C contents. The amorphous and nanocrystalline films showed a high Knoop hardness of ca. 500 kg mm(-2), while that of the crystalline films was found to be 300 kg mm(-2). The wear resistance of the film electrodeposited by the pulsed current method was remarkably good compared to that of the direct-current electrodeposition films, even though both films exhibited essentially identical microstructure and composition. The wear property was considered to be relevant to the restoration of the surface flatness of the film by the galvanic displacement deposition of Au during the pulse off time. (C) 2013 The Electrochemical Society. All rights reserved.

Ac impedance spectra of electrochemical systems are analyzed by considering adequate equivalent circuits, while the differentiation of responses for each elemental step is sometimes difficult. In this study, enlarged impedances were measured by lowering the temperature of a lithium ion battery (LIB) to make the separation of confusing responses easier. The impedance spectra obtained at the temperatures between -20 degrees C and 20 degrees C showed drastic change in sizes with shifting of the characteristic frequency. The analysis of impedance spectra using an equivalent circuit revealed changes in resistance of each component and shifting of the time constant for each elemental step. The frequency domain of impedance response of solid electrolyte interphase (SEI) was found to overlap with that of the inductive component of the outer electric lead at 20 degrees C in our study. The impedance measurement at the low temperatures is considered to be useful for the detection of the SEI and the accurate evaluation of LIB. (C) 2012 Elsevier B.V. All rights reserved.

Magnetite nanoparticles are expected to be applied in the medical field because of their biocompatibility and high saturated magnetization. In this paper, magnetite nanoparticles with a diameter of approximately 40 nm were evaluated for their safety by using mouse embryonic stem (mES) cells. First, various doses of magnetite nanoparticles were added to mES cells to find an optimal dose and to evaluate viability and keeping undifferentiated states of mES. The uptake of nanoparticles by mES cells was confirmed by using cytospin and transmission electron microscopy. Next, mES cells containing magnetite nanoparticles were collected by a magnet column 24h after the addition of magnetite nanoparticles, and the change in the ratio of those mES cells to the total mES cells was assayed by FACS 0, 4, 8, 12, 16, 24, 48 and 72 h after incubation. The result showed that the ratio decreased with time, indicating that the mES cells excreted the nanoparticles, for there was no change in the total number of cells. Based on these results, it was concluded that magnetite nanoparticles were safe to mES cells.

Matrix metalloproteinase (MMP) is known to be involved in chronic inflammation, tumor invasion, and carcinogenesis. To detect MMP-2, we examined the use of field effect transistors (FETs). After the addition of MMP-2 to a fibronectin (FN)-immobilized gate, negative value of FET response was observed, which indicates MMP-2 decreased the amount of negative charges arising from FN molecules. This FET device successfully detected MMP-2 by utilizing degradation of FN on the gate.

Superparamagnetic and ferromagnetic magnetite nanoparticles, with diameters of approximately 13 and 44 nm, respectively, were synthesized and their uptake amount and heating efficiency were evaluated for application to magnetic hyperthermia. Both nanoparticles had almost the same zeta-potential (+10.2 mV) and hydrodynamic size (∼1 μm) and there was no significant difference in their uptake amount 18 h after they were added to the medium. After internalization, the ferromagnetic nanoparticles incorporated in human breast cancer cells (MCF-7) showed a higher heating efficiency than the superparamagnetic nanoparticles when an external magnetic field (4 kW, 250 kHz) high enough to produce heat by hysteresis loss was applied, followed by cellular death of MCF-7 with high ferromagnetic nanoparticle content.

To analyze impedance response of an electrochemical system, it is important to model the system with an adequate equivalent circuit. In the present work, an equivalent circuit was designed for the analysis of lithium ion batteries with the contributions of a variety of diffusion parameters resulting from the various particle sizes for the cathode and the solid-electrolyte interphase formed on the anode particles, as well as electrochemical reactions and inductive components. Residual errors resulting from the data fitting was investigated for a variety of equivalent circuits used. The electrochemical impedance of the electrodes in commercial lithium ion batteries at various states of charge was analyzed to evaluate the proposed circuit. (C) 2012 Elsevier B.V. All rights reserved.

The degradation of the commercial Li ion battery was analyzed by electrochemical impedance spectroscopy, where our previous proposed equivalent circuit was applied. The degradation with the cycling was clearly explained by the main parameters of capacitive and resistive components, i.e., it responded until 300 cycles to the decrease in capacitive component, while after 300 to 550 cycles to the increase in resistive component.

A highly durable SiOC composite anode was prepared for use in lithium secondary batteries. The SiOC composite was synthesized by electrodeposition of SiCl4. The composite anode delivered a discharge capacity of 1045 mA h per gram of Si at the 2000th cycle and 842 mA h per gram of Si even at the 7200th cycle. The reason for the excellent cyclability was investigated by methods including field emission scanning electron microscopy (FESEM), scanning transmission electron microscopy with an energy dispersive X-ray analyser (STEM-EDX), and X-ray photoelectron spectroscopy (XPS). The results revealed that the excellent cyclability was achieved by the homogeneous dispersion of SiOx and organic/inorganic compounds at the nanometre scale. The structural uniformity of the SiOC composite is believed to have suppressed the crack formation attributable to the stress resulting from the reaction of silicon with lithium during charge-discharge cycles.

FePt nanoparticles of uniform sizes, compositions, and crystal structures can be obtained by chemical synthesis. Additionally, the nanoparticles can be well dispersed by the adsorption of a surfactant on the nanoparticle surface. Previously, the immobilization of FePt nanoparticles on a thermal oxide Si substrate was carried out by chemical synthesis, utilizing the Pt-S bonding between the -SH functional group in (3-mercaptopropyl)trimethoxysilane, MPTMS and Pt in FePt nanoparticles. However, controlling FePt nanoparticle arrays by this synthesis method was very difficult. In the present study, we attempted to control the distortion of the arrangement of FePt nanoparticles using an MPTMS layer modified with a silane coupling reaction and a geometrical structure prepared by ultraviolet nanoimprint lithography (UV-NIL). In this study, the hole-patterns used for the geometrical structure on Si(1 0 0) were 200 nm wide, 40 nm deep, and had a 500 nm pitch. The 5.6 nm FePt nanoparticles were used to coat the hole-patterns by using a picoliter pipette. An XHR-SEM image clearly revealed that the FePt nanoparticles were successfully arranged as a single layer with an average pitch of 10.0 nm by PL-S bonding in the hole-patterns on Si(1 0 0). (C) 2010 Elsevier B.V. All rights reserved.

This paper demonstrates that antibody-modified field effect transistors (FETs), which were treated with bovine serum albumin (BSA) blocking, had quantitative capability for tumor marker detection in blood serum. Antibody-modified surface covered with 0.1% BSA effectively minimized nonspecific adsorption of blood proteins. Tumor markers with their isoelectric points of around 5 generated strong signals in body environmental pH (pH 7.4) in proteins with isoelectric points ranging from 3 to 10. Detection of a tumor marker alpha-fetoprotein in blood serum at required level for clinical diagnosis (10 ng/mL) was achieved. The obtained results suggest that the fabricated FETs be expected to practical application in medical fields for direct detection of multi-tumor markers from blood. (C) 2011 Elsevier B.V. All rights reserved.

A self-assembled monolayer (SAM) of L-homocysteine (L-Hcy) formed on the surface of a gold-deposited gate of a field effect transistor (FET) was used to differentiate between enantiomers of amino acids, for which the formation of diastereomeric metal complexes is fundamental for chiral discrimination. Here, we focus our attention on the dependence of the FET response on the analyte amino acids, the central metal ions involved in complex formation, and the solution pH. Using the L-Hcy SAM-modified gate with added Cu(II), notable negative FET responses were enantioselectively observed for the L-enantiomers of alanine (Ala), phenylalanine, and tryptophan, whereas differences in the FET responses between enantiomers were negligible for asparagine and aspartic acid. Regarding the enantioselectivity for Ala, the addition of Cu(II) was demonstrated to show higher selectivity as compared to other metal ions such as Co(II) and Ni(II). Moreover, for the addition of L-Ala and Cu(II), a particularly strong negative FET response was observed at pH 5.5. (C) 2011 Elsevier Ltd. All rights reserved.

A novel potentiometric method using an indium tin oxide (ITO) electrode, surface-treated with aminopropylsilane and disuccinimidyl suberate successively, has been developed for measuring serotonin (5-HT), 5-hydroxy-L-tryptophan (5-HTP), 5-hydroxy-indole-acetic acid (5-HIAA), and melatonin (MT) (N-acetyl-5-methoxytryptamine) in phosphate buffered saline (PBS) solution (pH 7.4). A linear concentration range of 1 nM to 100 mu M was obtained with a correlation coefficient of 0.995 for all target analytes. The minimum detectable concentration obtained was 0.1 nM for 5-HT and 1.0 nM for other analytes. The relationship between the molecular structure of the indole derivatives and the enhanced potential shift behaviour was also discussed. This simple and efficient method can be used to measure other neurotransmitters, as well.

The effect of surface modification of indium tin oxide (ITO) electrode on its potential response to tryptophan was investigated for ITO substrates with different surface roughness. It was found that a small difference in surface roughness, between similar to 1 and similar to 2 nm of R(a) evaluated by atomic force microscopy, affects the rest potential of ITO electrode in the electrolyte. A slight difference in In:Sn ratio at the near surface of the ITO substrates, measured by angle-resolved X-ray photoelectron spectrometry and Auger electron spectroscopy is remarkable, and considered to relate with surface roughness. Interestingly, successive modification of the ITO surface with aminopropylsilane and disuccinimidyl suberate, of which essentiality to the potential response to indole compounds we previously reported, improved the stability of the rest potential and enabled the electrodes to respond to tryptophan in case of specimens with R(a) values ranging between similar to 2 and similar to 3 nm but not for those with R(a) of similar to 1 nm. It was suggested that there are optimum values of effective work function of ITO for specific potential response to tryptophan, which can be obtained by the successive modification of ITO surface. (C) 2011 Elsevier Ltd. All rights reserved.

A novel SiOC composite anode material for a Li battery was realized by electrochemical co-deposition of Si, C. and O elements. The composite was deposited by reduction of SiCl(4) in a propylene carbonate based solution. After the initiation process by reduction of the composite in a Li(+) containing electrolyte solution, the SiOC composite was found to be about 3.3 mu m in average thickness and the composite performed as a Li battery anode with over 1000 mAh g(-1) of Si for more than 2000 cycles, and moreover have continued for 7000 cycles with gradual degradation. (C) 2011 Elsevier B.V. All rights reserved.

Many efforts have been paid to realize the superior anodes for future Li batteries in either the dry Ar atmosphere or the dry air atmosphere. In this work, in order to clarify the effects of such atmospheres, the most reactive anodes of Li were freshly electrodeposited under the dry Ar or under the dry air condition. The Solid Electrolyte Interface (SEI) formed during the electrodeposition of Li anodes is revealed to have a different chemical composition and protective feature. The Li deposited under the dry air was revealed to have longer cycle life in the electrolyte than that deposited in Ar, even in the electrolyte containing ionic liquid. From the XPS results, the SEI formed in dry air is proved to be different from that formed in Ar gas atmospheres. that is, the SEI formed in dry air consists of Li(2)CO(3) and Li nitride. In order to improve the performance of the anodes, the atmosphere for the initial preparation of the anode/electrolyte interface should be tuned. Crown Copyright (C) 2011 Published by Elsevier B.V. All rights reserved.

Nitrogen doped carbon nanocapsules (NCNCs) were synthesized as a non-noble electrocatalyst for the ORR using a simple and efficient route. The NCNCs exhibited higher activity than the commercial Pt/C catalyst, excellent stability, and resistance to methanol oxidation in the oxygen reduction reaction.

In this paper, we present a method of fabricating a rigid antibody-immobilized surface using electric activation of a glutaraldehyde (GA)-modified aminopropylsilyl surface for stable antibody-modified field effect transistors (FETs). Electric activation of the GA-modified gate surface of the FET reduces Schiff bases, which are easily hydrolyzed and collapsed, formed between GA and 3-aminopropyltriethoxysilane, resulting in preventing the immobilized antibodies from desorbing from the surface. The lack of Raman peaks that could be assigned to a Schiff base after the electrical activation of the GA-modified surface indicated that the electric activation had reduced the Schiff base. The use of the antibody-modified FETs has three advantages for the detection of antigens: increased sensitivity, distinct recognition ability, and improved reproducibility. A tumor marker, alpha-fetoprotein (AFP), was quantitatively detected up to a concentration of 10 ng/mL using the antibody-modified FET. The detection ability of the FET accomplished a cutoff value of hepatic cancer. The quantitative detection of AFP in a solution with contaminating proteins was also demonstrated. This electric activation method is applicable to other antibody-modified FETs.

On-chip fuel cells are promising power sources for future electronics and microdevice applications including on-chip sensors and micro-air-vehicles. Previously, we reported a small scale (0.4 mm wide and 6 mm long) on-chip fuel cell of an air-breathing, membrane-less and monolithic design, which exhibited the highest power for an on-chip fuel cell, 1.4 mu W (J. Am. Chem. Soc., 2008, 130, 10456). In order to improve the performance, precise understanding of the phenomena occurring in the cells is of primary importance. Thus, this paper focuses on understanding cell operation by using numerical simulation, and on implementing cell improvements based on the simulation results. The initial quantitative study concluded that the performance of the on-chip fuel cell was limited owing to oxygen-supply caused by cathode flooding. Thus, we experimentally added the hydrophobic ionomer (Nafion) onto the cell to reduce the influence of the flooding, and successfully increased the maximum power from 2.0 to 2.8 mu W. This power is considered sufficient for microsensor application. On the basis of additional simulation results, we show that performance may potentially be improved to over 100 mu W by increasing the effective surface areas of catalysts to a level comparable with methanol fuel cells. If successful, such performance enhancements would position the on-chip fuel cell as a viable candidate for future micro-devices, and point to promising directions for fuel cell development efforts.

This paper reviews our study of bit patterned media (BPM) using L1(0) (face centered tetragonal)-FePt nanoparticles. For the practical use of L1(0)-FePt nanoparticles to BPM, some breakthroughs are required: a highly ordered two-dimensional array of nanoparticles on a substrate, a controlled orientation of the axis of easy magnetization in vertical direction on a substrate. Previously, we reported about the achievement for uniformity FePt nanoparticles by controlling chemical synthesis conditions. Moreover, we confirmed the selective chemical interaction Pt in the surface of FePt nanoparticles and SH group with (3-mercaptopropyl)tri-methoxysilane (MPTMS). This study presented a new hybrid technique combining the selective chemical bonding and a substrate with a geometrical grid in order to control the array of FePt nanoparticles with uniform direction of their magnetization. We succeed in preparing uniform array of nanoparticles on geometrical grid with size of 200 nm square prepared using ultraviolet nanoimprint lithography (UV-NIL).

This paper describes a practical method for predicting signals of an adsorbed protein detected by field effect transistors (FETs). The FETs detect the change of the surface charge caused by protein adsorption. The sensing signals strongly depend on an ionic strength of the buffer solution. The prediction of signals is useful for optimizing the strength. A calculation method using three-dimensional conformation structure of proteins was proposed for the prediction tool in the latest paper citing biotin-avidin interaction as an example. To verify availability of the method for alternative adsorbed protein, an adsorption model of streptavidin, which also has a binding ability to biotin, was investigated. Streptavidin has little charge in a buffer solution at pH 7.4 calculated from the method. The results suggest that the signals caused by adsorption of streptavidin were barely detectable using a biotinylated FET.

Herein we report that the in vitro gene transcription-translation efficiency can be dramatically enhanced by gold nanoparticles of 5nm in diameter. The addition of less than or equal to 1.2 nM of gold nanoparticles of 5 nm in diameter into rapid-translation-system (RTS) reagents increased the transcription-translation efficiency up to 30% and shortened the reaction time to 4 h, with the same or higher translation yields. Gold nanoparticles did not decrease the yields' bioactivity. The results show that gold nanoparticles of 5 nm may act as a bio-catalyst in the RTS reaction. This innovation has great potential in applications such as large-scale protein fabrication, gene transcription-translation regulation, and studies of structure and function of toxic protein. © 2011 DX. C, et al.

A novel transmission line (TML) model is proposed for the impedance analysis, which is nondestructive measurement, on degraded cathode catalyst layers in polymer electrolyte fuel cells (PEFCs). The test PEFC consisted of 1.0 mg/cm(2) of Pt-Ru as an anode catalyst, 1.0 mg/cm(2) of Pt as a cathode catalyst, and Nafion 212 as an electrolyte. The model counts the distribution of the oxygen reduction reaction (ORR) at the inside and outside of agglomerates of the carbon supported catalysts. We demonstrated the importance of the distribution of the ORR for achieving excellent agreement between the calculated and experimental data. The change in parameters obtained by impedance analysis with the TML model was verified by destructive tests, such as transmission electron microscopy, field emission scanning electron microscopy, cyclic voltammetry, micro-Fourier transform infrared spectroscopy and nitrogen adsorption-desorption measurements. Variations of the parameters such as the charge transfer resistance, the double layer capacitance, and the ionic resistance inside and outside the agglomerates of the carbon supported catalysts could be explained by multiple considerations of these destructive test results. Impedance analysis with the TML model offers the possibility understanding the state of degraded cathode catalyst layers in membrane electrode assemblies without the need for disassembling PEFCs. (C) 2011 The Electrochemical Society. [DOI: 10.1149/1.3610988] All rights reserved.

In order to improve the magnetic intergranular isolation between the magnetic grains in the SmCo5 perpendicular magnetic recording media, the palladium nuclei deposited by an electrochemical process were introduced into a sputter deposition process of the SmCo5 film. A few nanometer size Pd nuclei were electrochemically deposited on the sputtered Cu underlayer by a displacement deposition (chemical plating). The sizes of Pd nuclei were controlled by adjusting the Pd ion concentration in electrolyte solutions. The magnetic domain size in Sm-Co layer deposited on Pd nuclei / Cu / Ti underlayer became smaller and the magnetization reversal process was changed from the wall motion to the coherent rotation. Moreover, the read/write characteristics were improved at higher linear recording densities. (C) 2011 Published by Elsevier B.V. Selection and/or peer-review under responsibility of the Organising Committee of the 9th Perpendicular Magnetic Recording Conference

The microstructure of electrodeposited nano-crystalline Au-Ni film was investigated by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning transmission electron microscopy (STEM). Carbon was found to be included in the deposit, and the state of bonding and dispersion of the carbon and its effect on the microstructure of Au-Ni film were studied. Nano-crystalline films were found to be composed of Au-rich crystalline phase and Ni-rich phase, and the latter consisted of crystalline and amorphous phases. The amorphous phase contained a large number of carbon particles measuring 5-20 nm. TEM and STEM examinations showed that the large carbon particles possess a graphite-like structure with some of the particles being arranged in arrays. Mechanism of the carbon inclusion was discussed based on the results of XRD and the composition analysis of Au-free Ni film electrodeposited from a cyanide-containing bath. These results showed that carbon is co-deposited with Ni as nickel carbide and also as carbon particles. It is concluded that the inclusion of carbon and the coexistence of Au and Ni are the conditions necessary for the formation of amorphous structure of the electrodeposited Au-Ni alloy film. (C) 2011 The Electrochemical Society. [DOI: 10.1149/1.3579417] All rights reserved.

PdCo alloy is a promising catalyst for oxygen reduction reaction of direct methanol fuel cells because of its high activity and the tolerance to methanol. We have applied this catalyst in order to realize on-chip fuel cell which is a membraneless design. The novel design made the fuel cells to be flexible and integratable with other microdevices. Here, we summarize our recent research on the synthesis of nanostructured PdCo catalyst by electrochemical methods, which enable us to deposit the alloy onto microelectrodes of the on-chip fuel cells. First, the electrodeposition of PdCo is discussed in detail, and then, dealloying for introducing nanopores into the electrodeposits is described. Finally, electrochemical response and activities are fully discussed. Copyright © 2011 Satoshi Tominaka and Tetsuya Osaka.

The microstructure of electrodeposited Au-Ni films was investigated by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning transmission electron microscopy (STEM). Nano-crystalline films were found to be composed of three different phases: Au-rich crystalline phase, Ni-rich crystalline phase, and Ni-rich amorphous phase. Particles of carbon measuring 5 to 20 nm were also found in the deposit. It is assumed that the inclusion of a large amount of carbon particles causes the formation of the amorphous phase. The microstructure and the state of dispersion of the carbon particles were also investigated. The results of TEM and STEM observations showed that the carbon particles possess either the graphite structure or the amorphous structure with some of the particles being arranged in arrays. Scanning tunneling microscopy (STM) was performed to study the relationship between the structure of species adsorbed on the electrode surface and the process of carbon inclusion.

A mesoporous PtCu catalyst modified with a Ru submonolayer is successfully synthesized by a facile electrochemical process of electrodeposition, dealloying and Ru underpotential deposition. The material has a large specific surface area comparable to nanoparticles (11 m(2) g(-1)) and exhibits a promising catalyst activity for the methanol oxidation reaction.

Determination of protein charges under physiological conditions by field effect transistors (FETs) is challenging because of the screening effect by solution counter ions We showed that sugar-chain-modified FETs can detect proteins under physiological conditions Protein charges are detectable on the gate interface by applying sugar chains as receptors these sugar chains are short and highly flexible Threshold voltage shifts caused by adsorption of SSA lectin from Sambucus sieboldiana onto sialylglycan-modified FET showed a linear relationship with SSA concentrations under physiological conditions

SmCo5 alloy is a promising candidate for ultra-high-density perpendicular magnetic recording (PMR) media because of its high uniaxial magnetocrystalline anisotropy K-u of more than 1.1 x 10(8) erg/cm(3). Previously, we successfully achieved high K-u in a sputter-deposited SmCo5 thin film by introducing a Cu/Ti dual underlayer. However, in order to apply the SmCo5 films to practical PMR media, it is necessary to decrease medium noise. A granulated magnetic film comprising of small and magnetically decoupled grains is effective in reducing the medium noise. In this paper, we have proposed a new granular film that is fabricated by partial thermodiffusion of Cu between the Sm-Co continuous layer and the Cu underlayer, which is granulated using compositional segregation caused by the addition of Ta2O5. We have analyzed the magnetic properties, magnetic domain size, and magnetization reversal process of the proposed SmCo5 film. The magnetic domain size decreased and the magnetization reversal process changed from the magnetic-wall-motion mode to a coherent rotation mode to some extent on isolation of magnetic grains. The read/write characteristics of granulated SmCo5 double-layered media were also evaluated. The medium noise decreased and the signal-to-noise ratio increased for the granulated double-layered (PMR) medium. (C) 2010 Elsevier B.V. All rights reserved.

Sulfated zirconia is an inorganic solid superacid having sulfate groups covalently bonded to its surface. In this work, sulfated zirconia is synthesized by a solvent-free method to obtain it in the nanoparticle form. This nanostructured sulfated zirconia has been evaluated in terms of (i) chemical stability to hydrolysis and to hydrogen peroxide by thermogravimetric analysis, and (ii) influences on Pt catalyst activity by cyclic voltammetry using sulfated-zirconia dispersion as a supporting electrolyte solution. The results demonstrate that our sulfated zirconia is stable almost perfectly to hydrolysis but partly decomposed by a Fenton reagent containing hydrogen peroxide and Fe2+. In addition, we show that oxygen reduction activity of Pt catalyst in a sulfated-zirconia dispersion is comparatively high (specific activity at 0.9 V vs. RHE, i(0.9): ca. 17 mu A cm(-2)) compared to that in a 0.5 M sulfuric acid solution (i(0.9): ca. 15 mu A cm(-2)). Finally, we demonstrate that sulfated zirconia does not influence hydrogen oxidation reaction. These results lead us to conclude that sulfated zirconia is a promising proton conductor for fuel cells. (C) 2010 Published by Elsevier B.V.

The application of field effect transistor (FET) to chiral discrimination was investigated. An Au film vapor-deposited on a self-assembled monolayer (SAM) of (3-mercaptopropyl)trimethoxysilane, which was formed on the SiO2 gate of FET as an adhesive and insulating layer, stabilizes the drain current-gate voltage (I-d-V-g) property of FET. The modification by homocysteine(Hcy)SAM on the surface of Au-coated gate makes it possible for the FET to distinguish between the enantiomers of alanine (Ala). Namely, after the sequential addition of Ala and Cu(II) to a K2SO4 solution in this system, it was confirmed that the lateral shift of I-d-V-g curves for the FET corresponded to the chirality of Ala. With the L-Hcy SAM-modified gate, a notable negative shift was observed for L-Ala, whereas the shift observed with D-Ala was much smaller. In contrast, opposite results were obtained with D-Hcy SAM. Results of quartz crystal microbalance measurement suggested that such an FET response was originated from the enantioselective formation of diastereomeric Cu complexes with Ala molecules on the Hey SAM. This system was demonstrated to respond quantitatively to one enantiomeric form of Ala in mixed solutions of two enantiomers as well as in pure enantiomeric solutions (C) 2010 Elsevier Ltd. All rights reserved.

A Sm-Co-CrTa granular layer between a Sm-Co continuous layer and a Cu underlayer was prepared in order to improve magnetic properties and magnetic reversal process of Sm-Co perpendicular film. A phase of CrTa alloy in Sm-Co-CrTa layer has a role in control of Cu partial interlayer diffusion between the Sm-Co continuous layer and the Cu underlayer. The Cu diffusion provides the partial crystallization of SmCo5 in the continuous layer. Although the perpendicular coercivity of films decreased slightly by introducing the CrTa alloy into Sm-Co layer, the magnetic intergranular exchange interaction in the films was drastically improved. Size of average magnetic cluster became smaller and magnetization reversal process was changed from a wall-motion to a coherent rotation for increasing the thickness ratio of Sm-Co-CrTa/Sm-Co layers. We confirmed that an addition of Sm-Co-CrTa layer is effective to reduce the intergranular exchange interaction in Sm-Co perpendicular films without deterioration of perpendicular magnetic anisotropy.

A perpendicular mesoporous platinum film is used as a model electrode to clarify the effectiveness of catalysts inside agglomerates of fuel cell catalyst layers on the basis of experimental facts. The analysis clarifies that: (i) Pt surface even apart from Nafion ionomer phase can be electrochemically active: (ii) its response is different from that of the surface covered with ionomer; and (iii) ionic resistance in pores filled with pure water is too high (ca. 0.18 M Omega cm) for fuel cell reactions to smoothly occur. We conclude that such catalysts in pores filled with pure water are ineffective for fuel cell reactions due to the high ionic resistance, though their catalytic activity is possibly higher than that of the catalysts covered with Nafion. (C) 2009 Published by Elsevier B.V.

Fabricating reference field effect transistor (FET) sensors instead of reference electrodes are important for the miniaturization and variegated applications of FET sensors. To make a reference FET, the gate surface of FET was modified with the self-assembled monolayer (SAM) of n-octadecyltrimethoxysilane (ODS). Though an ODS-SAM FET had low pH-sensitivity, it was cation-sensitive. This work demonstrates the relation between the surface morphology and the cationic and pH-sensitivity of ODS-SAM FETs. A roughness parameter of atomic force microscope images. the mean summit curvature (Ssc) has correlation with the cationic and pH-sensitivity of ODS-SAM FETs.

This communication reports the synthesis of mesoporous Pd-Co dendrites with both a unique hierarchical porosity and a large surface area by the combination of electrodeposition and dealloying. The resultant mesoporous dendrites consist of microparticles with a diameter of a few hundred nanometers, and the particles have mesopores with around 10 nm width. The mesoporous dendrites are found to be Pd8Co2, to be composed of pure Pd crystalline phases and amorphous Pd-Co phases, and to be covered with Pd-skin layers. This catalyst exhibits a high activity in the oxygen reduction reaction. Thus, this novel catalyst is attractive as a catalyst for on-chip fuel cells. which require catalysts to be deposited precisely onto tiny current collectors. (C) 2009 Published by Elsevier B.V.

Potential response of indium tin oxide (ITO) electrode modified by treatment with disuccinimidyl suberate (DSS) was investigated to various target molecules. Distinctively, the DSS-modified ITO electrode exhibited a potential shift to the molecules possessing an indole group such as tryptophan, tryptamine and indole propionic acid, while little response to benzoic acid, phenylalanine, proline, proline amide, and arginine was observed. In addition, the combination of this specificity to indoles and enantioselective affinity of human serum albumin (HSA), which was additionally immobilized on the DSS-modified ITO electrode, brought about enantioselective potential response to tryptophan.

Carbon inclusion and its effect on the crystallinity of electrodeposited Au-Ni alloy films are discussed based on the results of X-ray diffraction (XRD) spectroscopy, chemical composition analysis, X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Under an optimum set of conditions, both citrate bath and pyrophosphate bath yield Au-Ni alloy deposits, which are amorphous to the XRD measurement. The carbon content of the amorphous deposit is higher than that of the crystalline deposit, and this trend is observed for deposits from both citrate and pyrophosphate baths. Experimental results are presented, showing that the amorphous deposits from both citrate and pyrophosphate baths contained a comparable amount of carbon, which indicates that CN from KAu(CN)(2) is the major source of carbon inclusion in the deposits from both baths. The results of XPS and, more clearly, Raman spectroscopy show that the amorphous Au-Ni deposit contains a large amount of carbon in the amorphous state, which apparently forms as a result of the decomposition of CN, whereas only the crystalline deposit contains carbon in the form of CN. It is concluded that carbon inclusion and the state of included carbon play a significant role in the process of creating the amorphous structure of Au-Ni alloy electrodeposits.

This article discusses differences in physicochemical properties such as solubility and melting point between (S)-thalidomide and (RS)-thalidomide based on crystal structures determined by X-ray diffraction experiments. Investigation of such differences is of great importance because thalidomide has attracted considerable attention again due to its wide-range bioactivity for intractable diseases. In this article, structures of hydrogen-bonded rings were compared between asymmetric homochiral dimers in (S)-thalidomide crystal and symmetric heterochiral dimers in (RS)-thalidomide crystal. The heterochiral dimer was evaluated to be more stable than the homochiral dimer by the energy calculations for hydrogen-bonded rings in those dimers. These results indicate that differences in physicochemical properties between enantiomeric and racemic thalidomides originate from the difference of structural stability between homochiral and heterochiral dimers.

Stem cells nanotechnology has emerged as a new exciting area, and holds great potential for research and development of stem cells as novel therapeutic platforms for genetic, traumatic, and degenerative medicine. Vital to the success of this technology are approaches that reproducibly facilitate in vivo cell tracking, expansion, differentiation, and transplantation. Herein we reported the effects of CdSe/ZnS quantum dots covered multi-walled carbon nanotubes (FMNTs) on mice embryonic stem cell line CCE cells. The FMNTs were prepared by plasma surface treatment and characterized by high resolution transmission electron microscopy (HR-TEM), and incubated with murine ES CCE cells for 1 to 28 day.These ES cells were observed by confocal laser scanning microscopy, and were analyzed by real time reverse transcription-polymerase chain reaction (RTPCR), flow cytometry (FCM) and MTT method. Results showed that prepared FMNTs exhibited green fluorescent signal, could enter into ES cells in time-dependent means, more than 20 μg ml-1 FMNTs induced ES cells become smaller and smaller as the incubation time increased, and inhibited cell growth in dose-and time-dependent means, induced apoptosis of ES cells
conversely, 5 μg ml-1 FMNTs could markedly stimulate the expression of Sox1 and Hsp27, and inhibit expression of OCT4 in ES cells, FCM analysis showed that differentiation marker Flk-1 exhibited higher expression compared with control ES cells. In conclusion, high dose of FMNTs can inhibit proliferation of ES cells, low dose of FMNTs can improve the differentiation of ES cells, FMNTs can have potential applications in in vivo tracking, imaging and regulation of the proliferation and differentiation of ES cells. © 2010 D. Cui, et al.

A mesoporous PdCo sponge-like nanostructure was successfully synthesized by the combination of electrodeposition and dealloying, and was evaluated as a catalyst for the oxygen reduction reaction of fuel cells. The synthesized film had a sponge-like mesoporosity consisting of 5-30 nm thick ligaments with pores of tens of nanometers. Its porosity was estimated to be ca. 62%, suggesting that the oxygen transport in the film was smooth. The resultant composition was Pd93Co7, whose crystalline phase was determined to be a solid solution of Pd92Co8 by X-ray diffractometry. This degree of alloying is known to induce the most desirable lattice contraction into a Pd catalyst for the oxygen reduction reaction. Actually, the mesoporous PdCo catalyst had a higher specific activity than the Pt catalyst in the potential range of <0.85 V vs. SHE, i.e., the potential range of interest for fuel cell operation. This fascinatingly higher catalytic activity was attributable to the preferable reaction mechanism, because the PdCo electrode had a lower Tafel slope (43 mV decade (1)) than a typical Pt electrode (71 mV decade(-1)).

This paper describes an overview of our research with the title of Establishment of Electrochemical Device Engineering. The goal of this work is to develop systematic methodologies for the creation of advanced materials and devices based on the design of the interface, which is derived from our study of the practical application of Electrochemical Nanotechnology. We introduce three-, two-, and zero-dimensional viewpoints to the design of the interface between electrode and electrolyte based on electrochemical nanotechnology. In this manuscript, two-dimensional design is explained first and then three- and zero-dimensional topics are mentioned.

Field effect transistors (FETs) may respond to charge variations occurring when proteins are adsorbed to the gate surface. The electrolyte electrostatic screening allows a practical detection of charges that are only within a distance of approximately the double layer thickness, which is related to the Debye length in the electrolyte. Hence, operating the FET biomolecular sensors at the highest possible ionic concentration improves reproducibility; however, it may reduce the signal if the concentration is too high. Here, we propose an optimization method of the buffer ionic concentration using a figure of merit "charge number," Z(d), which is defined as the ratio between the effective number of the surface charges and the number of immobilized molecules. The theoretical Z(d) was calculated using a three-dimensional conformation data taken from the Protein Data Bank. The Z(d) was obtained from the total number of four charged amino acids of avidin, arginine (positive), lysine (positive), aspartic acid (negative), and glutamic acid (negative), which are within the double layer length from the surface. To verify this model, we chose avidin-biotin interaction. The experimental Z(d), which was obtained for three buffer concentrations, matched the theoretical Z(d). This method shortens the solution calibration time and reduces the analyte amount. (C) 2010 The Electrochemical Society. [DOI: 10.1149/1.3491764] All rights reserved.

This study on future ultrahigh density magnetic recording devices aims to develop a technique for arranging FePt nanocubes on a substrate by using organosilane as an interlayer. An array of FePt nanocubes was formed by chemical synthesis, utilizing the Pt-S binding between the SH functional group in (3-mercaptopropyl)trimethoxysilane and Pt in the FePt nanocubes. The morphology of the FePt nanocube array on the substrate was characterized using atomic force microscopy and plan-view scanning electron microscopy, which revealed that the array was a monolayer. After SiO(2) was coated by chemical vapor deposition as a protective layer for sintering prevention, annealing was carried out at 900 degrees C for 3 h in a reducing atmosphere to transform the crystal structure of the FePt nanocubes to the L1(0) phase. X-ray diffraction results revealed that the annealed FePt nanocube array had a FePt(110) orientation and L1(0) phases such as (001) and (110). The Pt-S binding did not obstruct the L1(0) ordering of FePt. Consequently, a method for arranging nanoparticles by using the organic molecules with functional groups that can interact with nanoparticle selectivity as an interlayer can be applied as a formation technique for arranging a wide range of nanoparticles. (C) 2010 The Electrochemical Society. [DOI:10.1149/1.3465631] All rights reserved.

Internalization of magnetite nanoparticles with diameter of approximately 40 nm into normal and cancer cells was examined by microscopic observation and flow cytometry. Magnetite nanoparticles were synthesized by hydrolysis in an aqueous solution containing ferrous chloride with organic amines as a base. It was demonstrated that the difference in surface charge of magnetite nanoparticles brought about the difference in uptake efficiency. The nanoparticles with positive charge showed higher internalization into human breast cancer cells than the nanoparticles with negative charge, while the degree of internalization of the positively- and negatively-charged nanoparticles into human umbilical vein endothelial cells (HUVEC) was almost the same.

The application of localized surface plasmon resonance (LSPR) of gold nanoparticles for the detection of biotin-streptavidin binding, as a typical biological reaction, was investigated by using optical waveguide spectroscopy, and two different modes for the use of gold nanoparticles, one as a probe and the other as a label were compared with each other. The combination with optical waveguide spectroscopy was found to bring about a high sensitivity for the biomolecular detection system using LSPR of gold nanoparticles in both modes. In particular, the mode using gold nanoparticles as a label was demonstrated to be of advantage to devising proper procedures for using nanoparticles and evaluating actual response relevant to the phenomenon concerned, and thus to sensitive detection.

Catalyst layers of direct methanol fuel cells (DMFCs) are modified by in situ electropolymerization of m-aminobenzenesulfonic acid. By using electrochemical impedance spectroscopy and porosimetry, this modification is found to add polymer electrolyte into primary pores (<10 nm), where ionic resistance is high for lack of polymer electrolyte (i.e., Nafion), and the additional electrolyte successfully decreases the ionic resistance by 10-15% compared to the plain carbon surface with a slight ion-conductivity (>40 k Omega cm). In view of methanol oxidation characteristics, this modification decreases the resistance by ca. 25% (from 5.1 Omega cm(2) to 3.7 Omega cm(2)) at 0.6V vs. DHE, resulting in the increase in the cell voltage of DMFC test by ca. 20 mV. The clear relation between the performance and the microstructures is concluded to be helpful to understand the performance of fuel cell electrodes in detail. (C) 2009 Elsevier B.V. All rights reserved.

As potential high capacity anode materials for lithium ion batteries, the Sri and Ni-Sn alloy coatings have been investigated by many electrochemical researchers. However, their mechanical properties have not been extensively Studied, despite the fact that such anode films may fail mechanically during service. Thus, in this study nanoindentation and nanowear tests have been performed. Nanoindentation tests reveal that the ability to carry the load dramatically reduces in the Sri coating after one charge-discharge cycle which makes the plastic strain accumulation in the copper Substrate play a greater Contribution to crack formation and propagation in repeated charge-discharge cycling. Upon the nanoindentation analysis, it also shows that the pores formed by lithiation/delithiation can easily collapse at low loads. Furthermore, nanowear tests explore that the damage resistance of the Sn-Ni alloy film significantly improves after one charge-discharge cycle but it decreases in the Sri film after the same charge-discharge cycle; this explains why the degradation rate of the Ni-Sn alloy is slow after the first charge-discharge cycle and why the high capacity is maintained in further cycling. The links between the mechanical characterization and the degradation in charge-discharge cycling are also discussed. (c) 2008 Elsevier Ltd. All rights reserved.

Non-platinum nanoparticles (Pd, Au, PdAu) have been prepared by sonochemical synthesis. The nanoparticle-modified electrodes showed improved catalytic activity for oxygen reduction compared with Pt nanoparticles in alkaline solution even in the presence of methanol.

Sheet-shaped carriers, having both obverse and reverse surfaces and thus a large contact area for targeting a site, have several advantages over spherical-shaped carriers, which have an extremely small contact area for targeting sites. Here, we proposed a novel method to prepare a free-standing ultrathin and biocompatible nanosheet having heterosurfaces, by a combination of four processes: (1) specific adsorption of recombinant human serum albumin (rHSA) molecules onto a patterned octadecyltrimethoxysilane self-assembled monolayer region (ODS-SAM), (2) preparation of nanosheets of rHSA molecules bearing thiol groups (SH-rHSA) via two-dimensionally disulfide crosslinking, (3) surface modification of the resulting nanosheet, and (4) preparation of the free-standing nanosheet by detachment from the ODS-SAM. The SH-rHSA molecules at pH 5.0 and a concentration of 1 microg/mL were specifically adsorbed on the patterned ODS-SAM regions by hydrophobic interaction, and were two-dimensionally crosslinked in the presence of copper ion as an oxidant. The rHSA-nanosheets were then simply detached from the ODS-SAM by treatment with surfactant. We succeeded in the preparation of rectangular (10 microm x 30 microm) and ultrathin (4.5 +/- 1.0 nm) rHSA-nanosheets on a patterned ODS-SAM, and could also obtain free-standing rHSA-nanosheets having heterosurfaces by surface modification with fluorescent latex beads. Thus, the rHSA-nanosheets having heterosurfaces could be regarded as a new biomaterial for drug carriers, hemostatic reagents, wound dressing for burn injury, and so forth.

Carbon-supported Pd-Sn (Pd-Sn/C) catalyst was prepared under ultrasonic irradiation, and its electrocatalytic activity for oxygen reduction reaction (ORR) was evaluated in 0.5M KOH. TEM images showed that the prepared Pd-Sn/C catalyst particles are smaller in average size than carbon-supported Pd (Pd/C) catalyst particles. XRD and XPS results indicated the small particle size and the electronic interaction between Pd and Sn for the Pd-Sn/C catalyst. The Pd-Sn/C catalyst has a higher ORR activity than the Pd/C catalyst in alkaline media. In addition, the Pd-Sn/C catalyst showed a lower Tafel slope and a larger number of electrons transferred for ORR, compared with those of the Pd/C catalyst. These results indicate that Sn influences both the kinetics and the mechanism of ORR. Based on these results, the Pd-Sn/C catalyst prepared by using ultrasonic irradiation can be expected as a promising ORR catalyst in alkaline media. (C) 2009 Elsevier B.V. All rights reserved.

Direct methanol alkaline fuel cell (DMAFC) using anion exchange membrane (AEM) was operated in passive condition. Cell with AEM exhibits a higher open circuit voltage (OCV) and superior cell performance than those in cell using Nafion. From the concentration dependences of methanol, KOH in fuel and ionomer in anode catalyst layer, it is found that the key factors are to improve the ionic conductivity at the anode and to form a favorable ion conductive path in catalyst layer in order to enhance the cell performance. In addition, by using home-made Pd-Sn/C catalyst as a cathode catalyst on DMAFC, the membrane electrode assembly (MEA) using Pd-Sn/C catalyst as cathode exhibits the higher performance than the usual commercially available Pt/C catalyst in high methanol concentration. Therefore, the Pd-Sn/C catalyst with high tolerance for methanol is expected as the promising oxygen reduction reaction (ORR) catalyst in DMAFC. (C) 2009 Elsevier B.V. All rights reserved.

Nanoparticles of Pd-Sn were prepared under various conditions by applying ultrasonic irradiation, and their electrocatalytic activity for oxygen reduction was evaluated in 0.5 M KOH. The average size of Pd-Sn nanoparticles thus prepared was about 3-5 nm. The Pd in Pd-Sn nanoparticles was found to be mostly in the metallic state. The electrocatalytic activity of the Pd-Sn nanoparticles for the oxygen reduction reaction (ORR) is greater than Pt or Pd nanoparticles in alkaline media. The molar ratio of Pd to Sn metal ions in the synthesizing solution, their initial concentrations, the concentration of ethanol, which increases primary hydrogen radicals during sonolysis, and the concentration of citric acid were found to affect the size distribution of the Pd-Sn nanoparticles, and therefore, those factors controlled the electrocatalytic activity for ORR. Particularly, the concentration of citric acid was found to be important for controlling the surface property on Pd-Sn particles to adjust the electrocatalytic activity for ORR. (C) 2009 Elsevier Ltd. All rights reserved.

The use of Tb3+ as a center ion and media to introduce more exogenously negative charges onto double-stranded DNA (dsDNA), can greatly enhance potentiometric signals produced by the shift of gate voltage of field effect transisitor (FET). Furthermore, different affinities of Tb3+ to normal and mismatched dsDNAs amplified the signal difference between their detections, which can improve the discrimination of single nucleotide polymorphism.

We developed a new quantitative detection method for an immunoreaction combining magnetite (Fe3O4) nanoparticle labeling with confocal Raman spectrometry. Magnetite nanoparticles are transparent, Raman active, and easily can be controlled easily by magnets in bimolecular reactions. Human Chorionic Gonadtropin (hCG) was selected as a target molecule for this investigation. Sandwich immunoreaction was performed on a dot-patterned substrate using two anti-hCG antibodies, which were the antibody immobilized on the substrate and the biotinylated antibody. The immunoreaction was microscopically visualized by reacting streptavidin-modified magnetite nanoparticles with the biotinylated antibody on the substrate. The adsorbed magnetite nanoparticles on the dot pattern were detected by Raman intensity imaging. A good linear relation between the integrated Raman intensity spectra at 220 cm-1 and hCG concentration was gained. This method may be applied toward the detection of other target molecules in the fields of biotechnology and biomedicine. © 2008 The Surface Science Society of Japan.

Copper films electrodeposited from acid sulfate baths containing conventional additives used in the damascene process for the fabrication of ultralarge-scale integration interconnects were analyzed quantitatively to investigate the relation between carbon content and electrical resistivity of the deposit. In the as-deposited state, the resistivity of deposits that did not exhibit self-annealing effects in scanning ion microscope examination increased almost linearly with carbon content in the range of 0.002-0.045 wt %. The deposits that exhibited self-annealing effects showed higher resistivity values at identical carbon contents. After self-annealing, resistivity values of all deposits varied almost linearly with carbon content. (C) 2009 The Electrochemical Society. [DOI: 10.1149/1.3054273] All rights reserved.

A facile and simple approach for the synthesis of nanosized iron oxide and oxyhydroxide using biogenic polyamines is described. At room temperature, the highly crystalline nanoparticles of magnetite (Fe3O4) with average sizes of 44 +/- 2 and 37 +/- 1 nm were synthesized with spermine and spermidine, respectively. The magnetite nanoparticles formed by the biogenic polyamines exhibited a ferrimagnetic behavior at room temperature. When the same reaction was carried out at low temperature, crystalline nanorods of lepidocrocite (gamma-FeOOH) with a high aspect ratio were formed. It was revealed that the lepidocrocite nanorods with an aspect ratio of 70 formed bundles, each of which consisted of several nanorods stacked together by the side on fashion. It was suggested that the nanorods are of single-crystalline nature and exhibit a superparamagnetic behavior at room temperature. As the reaction temperature increased from 40 to 70 degrees C, the formation of magnetite nanotetrapods, nanorods, and nanoparticles was observed depending on the reaction temperatures. Magnetic properties of products were demonstrated to depend on the morphology, the degree of crystallinity, and the presence of amorphous oxyhydroxide. (C) 2009 The Electrochemical Society. [DOI: 10.1149/1.3125767] All rights reserved.

Ti alloys are commonly used as dental and orthopaedic implants. It has been shown that surface topography can influence cell genesis, behaviour and growth. In this work we have electropolished and micro-patterned Ti-6Al-4V alloy to study the effect of surface topography on cell morphology. Electroetching was carried out in a flat cell under galvanostatic polarisation of 5.0 V and 9.0 V vs. SCE, using a 3.0 M H2SO4 - methanol electrolyte. Electropolishing conditions were achieved when the overpotential was 9.0 V. Micropatterning of Ti alloy substrates was carried out at the same potentials by etching through mask
a methanol stable SU-8 photoresist was used for this purpose. Human mesenchymal stem cells were seeded and grown on these substrates. It was found that surface nano and micro scale topography influenced cell numbers and morphology, respectively. ©The Electrochemical Society.

A facile and simple approach has been described for the synthesis of magnetite nanoparticles and iron oxyhydroxide nanorods using biogenic polyamines. At room temperature, highly crystalline magnetite particles with average size of 44 ± 2 and 37 ± 1 nm were synthesized with spermine and spermidine, respectively. The formation of nanoparticles was characterized with TEM, HRTEM, XPS and SQUID. The magnetite nanoparticles formed by the biogenic polyamines exhibits ferrimagnetic behavior at 300 K. When the reaction was carried out at low temperature, high aspect ratio, well crystalline nanorods were observed. X-ray diffraction and Infrared spectroscopy suggests that the nanorods correspond to lepidocrocite (γ-FeOOH). TEM analysis shows each bundle consisting of several nanorods stacked together by side on fashion. γ-FeOOH nanorods with high aspect ratio of 70 were observed. The SQUID analysis reveals that the lepidocrocite nanorods exhibit superparamagnetic behavior at room temperature. ©The Electrochemical Society.

The performance of an on-chip direct methanol fuel cell of monolithic design with an active-type system was improved more than 6-fold up to > 100 mu W by using hydrogen peroxide as an oxidant solution instead of dissolved oxygen, but the energy-loss caused by strong capillary forces required a redesign of both microchannel size and the system.

An on-chip fuel cell, of membraneless, air-breathing and monolithic design, was proven to operate on a different fuel (methanol, ethanol or 2-propanol) solution containing an acidic ion-conductor (sulfuric acid) or a neutral one (phosphate buffer).

All-wet process was developed for fabricating diffusion barrier layer and Copper wiring for ultra large scale integration (ULSI) by means of a combination technique of electroless deposition and surface modification of Pd-activated ligand-bearing organic layer. In this paper, we performed detailed analysis of the Pd-activated ligand-bearing organic layer. Moreover, we successfully deposited thin electroless NiB layer on the Pd-activated molecular layer of 3-[2-(2-aminoethylamino)ethylamino]propyltrimethoxysilane (TAS) in a small reactor at a low temperature in a few minutes. ©The Electrochemical Society.

Here we report fabrication of tiny on-chip fuel cells on polymer films. Since on-chip cells which we have so far fabricated on silicon substrates through a series of microfabrication procedures are of a simple microchannel-based design, their fabrication on a polymer substrate by molding is attractive in terms of the rapid fabrication and of the inexpensive fabrication procedures and materials. To do so, a nickel mold was first prepared by electroplating from the conventional silicon-based cell, i.e., a master, and then the cell was replicated on cycloolefin polymer films by hot embossing. The microchannel thus replicated on the polymer film was confirmed to be almost identical to the silicon master by observation with a confocal microscope. Finally, Au current collectors sufficiently adhesive to the polymer were successfully deposited after the surface modification by an oxygen plasma treatment.

For completion of on-chip field effect transistor (FET) biosensors, it is essential to produce a reference FET instead of a reference electrode that uses an inner electrolyte. In this study, a light-addressable potentiometric sensor (LAPS) modified by a self-assembled monolayer (SAM) of octadecylsilane (ODS) was pH-insensitive (-1.5 mV/pH), but it was sensitive to ionic strength as was reported in polymer-gate FETs. Our purpose was to make clear the problems of the evaluation methods of ODS-SAM FETs concerning pH and ionic responses and the effect of the surface morphology to improve a reference SAM-FET. An ODS-SAM LAPS and FET were deposited under different conditions. pH and ionic responses, roughness measured by atomic force microscope, and contact angle (CA) were greatly changed by the difference in morphology of the ODS-SAM. ODS coagulation raised the CA. It is difficult to distinguish the ODS-SAM with and without ODS coagulation only by CA, but CA is utilizable for observing the state of hydroxyl groups on the surface without ODS coagulation. ODS coagulation caused the pH response with the ODS-SAM but decreased the ionic response of the LAPS. Controlling the surface morphology of the ODS-SAM is important to suppress the pH and ionic sensitivities for an in vivo applicable reference FET.

A novel concept of fuel cells, i.e., bendable fuel cells, is proposed and demonstrated by the fabrication of on-chip fuel cells on cycloolefin polymer films. This approach overcomes the brittleness and cost problems, i.e., a troubling aspect of miniaturized devices, of on-chip fuel cells.

We investigated the electroless CoWP/NiB diffusion barrier layer for ultralarge-scale integration (ULSI) interconnection by forming the immobilizing Pd catalyst on an organosilane layer. When the electroless CoWP film was formed directly on a Pd-activated organosilane layer, it became islandlike and did not form a continuous layer. When it was formed on an electroless NiB deposited on a Pd-activated organosilane layer, the electroless CoWP film was uniform and formed a continuous layer 10 nm thick. The transmission electron microscopy images of the interfaces of Cu/CoWP/NiB/SiO2 showed that, at an annealing temperature up to 400 degrees C for 30 min, the interfaces remained unchanged and clear, showing no trace of Cu diffusion into the SiO2 substrate. In-plane X-ray diffraction patterns indicated that the CoWP/NiB film had an amorphous structure and was stable against heat-treatment up to 500 degrees C for 30 min. An evaluation of sheet resistance measurements suggested that the CoWP/NiB film shows appropriate barrier properties for Cu diffusion up to 400 degrees C. The CoWP/NiB film was used as a seed for electroless Cu plating. Trenches 100 nm wide were coated with a 10 nm CoWP/NiB barrier followed by successful trench filling by electroless Cu plating.

A process was developed for producing a barrier layer of NiB by means of electroless deposition on an underlayer of Pd-activated organosilane monolayer formed on the insulator. An attempt was made to decrease the thickness of the NiB layer without adversely affecting its barrier property to make it compatible with further miniaturized ultralarge-scale integration (ULSI) devices of the future. This aim was achieved by using 3-[2-(2-aminoethylamino)ethylamino]propyltrimethoxysilane (TAS) as the underlayer between the NiB layer and the substrate. By using TAS instead of 3-aminopropyltriethoxysilane (APTES) which was used in our previous study, the minimum acceptable thickness of the NiB barrier layer was successfully reduced to 6 nm. The copper deposit formed on the barrier layer in trenches was free of defects, and it was stable even after annealing at 400 degrees C for 30 min.

Preparation of human immune T cells containing iron-oxide nanoparticles was carried out for the development of magnetically mediated immunotherapy. Peripheral blood lymphocytes (PBLs) after the incubation with magnetite nanoparticles were found to contain measurable ferric ions, which suggested the incorporation of magnetite nanoparticles. Transmission electron microscopic (TEM) study indicated that the incorporation of magnetite nanoparticles was mediated by endocytosis of PBLs. Furthermore, the effects of dosages and diameter of magnetite nanoparticles on the magnetite incorporation were investigated, and it was demonstrated that the increase in dosage promoted the incorporation of nanoparticles and the uptake into PBLs was more effective for magnetite nanoparticles, which formed smaller aggregations in medium. Finally, the demonstration of magnetite incorporation into enriched T cells and tumor antigen-specific cytotoxic T lymphocyte (CTL) line promises the achievement of magnetically mediated immunotherapy with tumor-specific CTLs containing magnetic nanoparticles.

Sulfated zirconia nanoparticles are evaluated as a possible alternative for a solid proton conductor in a fuel-cell catalyst layer. Two methods are applied for the synthesis of the nanoparticles, i.e.: (i) a conventional method treating ZrO2 particles in sulfuric acid, and (ii) a solvent-free method directly synthesizing sulfated zirconia nanoparticles through the thermal decomposition of a mixture of ZrOCl2 and (NH4)(2)SO4. The nanoparticles synthesized by the solvent-free method have a size of 5-10 nm and an amorphous structure, and moreover their properties are promising in view of the application. In particular, the proton conductivity of the nanoparticles is high enough, i.e. of the 10(-2) S cm(-1) order, to be comparable to that of Nafion. Even though they possibly reduce the activity of Pt catalyst, layers containing sulfated zirconia as a proton conductor prove to be active as catalyst in fuel cell prototypes. Compared with conventional, Nafion-based cells, the maximum power density of the cells using sulfated zirconia is about one third. We believe that improvement in the preparation procedures for catalyst layers and membrane electrode assemblies will improve the cell performance. Therefore sulfated zirconia can be a valid proton conductor for fuel cell application. (C) 2008 Elsevier B.V. All rights reserved.

The present study aims at extending the possibility of utilizing bulky molecules such as proteins for fabricating electrochemical chiral sensors using an indium tin oxide (ITO) electrode. Enantioselective potential response of the human serum albumin (HSA)-modified ITO electrode was observed for tryptophan (Trp) when HSA was immobilized on an ITO electrode surface modified with disuccinimidyl suberate (DSS). In this sensing system. the enantioselective interaction between HSA and Trp is detected through the chemically reactive DSS group immobilized on the ITO electrode. (C) 2008 Elsevier B.V. All rights reserved.

Magnetic circular dichroism (MCD) and X-ray absorption spectra (XAS) at the Co L(2,3)-edge of [Co/Pd](20) and [CoB/Pd](20) multilayered films, which were fabricated at 260 degrees C with different magnetic layer thicknesses (delta), have been measured. The lineshapes of XAS-MCD show that the electronic state of Co 3d of the films hardly changes even when sputtered at higher temperatures. The expectation values of orbital and spin angular momentum (&lt; L(z)&gt; and &lt; S(z)&gt;) are estimated using the sum rule, and it is found that &lt; L(z)&gt;/&lt; S(z)&gt; in delta&lt;0.5 nm is larger than that in delta&gt;0.5 nm. (C) 2008 Elsevier B. V. All rights reserved.

An SmCo(5) alloy is a promising candidate for ultra-high density magnetic recording media because of its strong uniaxial magnetocrystalline anisotropy, whose constant, K(u), is more than 1.1 x 10(8) erg/cm(3). Recently, we successfully obtained high perpendicular magnetic anisotropy for a sputter-deposited SmCo(5) thin film by introducing a Cu/Ti dual underlayer. However, it is necessary to improve magnetic properties and read/write (R/W) characteristics for applying SmCo(5) thin films to perpendicular magnetic recording media. In this study, we focused on reduction of magnetic domain size and change of a magnetization reversal process of SmCo(5) perpendicular magnetic thin. films by introducing carbon (C) atoms into the constituent Cu underlayer. The magnetic domain size became small and the ratio of coercivity (H(c)) against magnetic anisotropy (H(k)) which is an index of the magnetization reversal process was increased by adding C atoms. We also evaluated the R/W characteristics of SmCo(5) double-layered media including C atoms. The medium noise was decreased and signal-to-noise ratio increased by introducing the C. The addition of C into the Cu underlayer is effective for changing the magnetization reversal process, reducing medium noise and increasing SNR. (C) 2008 Published by Elsevier B. V.

Nanoparticles of FePt were prepared in two different ionic liquids (ILs). Because IL serves not only as a solvent but also as a surfactant, the particles prepared could be dispersed stably in hexane without adding other surfactants. The size distribution of the particles was found to be narrow without depending oil a size-selection process such as centrifugation. In addition, the particle sizes and composition were found to depend on the kind of IL employed.

The stereospecificity of a self-assembled monolayer (SAM) of homocysteine formed on the (111)-oriented gold surface toward the molecules with two chiral centers was investigated. Redox behaviors of catechins, which are electrochemically active molecules with two chiral centers, were analyzed with cyclic voltammetry by using a gold electrode modified with one enantiomeric form of homocysteine. The homocysteine SAM of one enantiomeric form was demonstrated to block the redox reaction of one enantiomer of catechin or epicatechin greater than that of the other, with cross inversion for the other enantiomer, in acidic solution. In addition, the homocysteine SAM on the gold electrode was suggested to recognize the chirality of one of the two chiral centers in catechin and epicatechin. (C) 2008 Elsevier Ltd. All rights reserved.

This paper proposes a novel design for a microfuel cell as an on-chip power source and demonstrates its fabrication and operation to prove the concept. Its simple design is important from the viewpoints of fabrication (e.g., replication), integration, and compatibility with other microdevices. In testing, the prototype cell was able to generate electric power (maximum: ca. 1.4 microW) on methanol without pumps under both neutral and acidic conditions. As for the size, the electrode part of the cell (two cathodes and one anode) is 400 microns in width and 6 mm in length. The evaluation demonstrated that the proposed design is a promising on-chip power source for miniature devices.

The process of preparation of FePt nanoparticles was investigated with emphasis on the effect of "growth temperature," at which the atomic diffusion between Pt-rich and Fe-rich phases leads to the formation of uniform nanoparticles. Consequently, it was demonstrated that by controlling, the growth temperature, the shape and crystallinity of FePt nanoparticles can be controlled. Oil the other hand, the size and composition were almost invariable at 5.6 +/- 0.5 nm and Fe53Pt47. respectively.

A perpendicular mesoporous platinum electrode with a flat surface is successfully synthesized by electrodeposition using titania nanopillars as template, and the electrochemical studies indicate that this material is a promising catalytic electrode for fuel cells because of its high surface area and perpendicular nanopores.

It was found that, by choosing an optimum bath composition, amorphous Au-Ni alloy containing up to 40 at.% of Au with respect to the sum of Au and Ni can be electrodeposited from a bath prepared by excluding tungsten from the Au-Ni-W bath that we developed previously. Elemental analysis showed that the deposit contains 15-20 at.% of carbon and 2 at.% of nitrogen. Hardness of this deposit is almost three times as high as that of the conventional hard gold. The electrical contact resistance measured against a pure gold wire is comparable to that of the hard gold. The amorphous structure of the Au-Ni deposit is stable at temperatures up to 300 degrees C for at least 1 h. The amorphous tungsten-free Au-Ni deposit is worthy of consideration for applications in the fabrication of micro- and nano-scale electrical contacts. (c) 2008 Elsevier Ltd. All rights reserved.

Pd-Co alloy has been recently proposed as a catalyst for the cathode of direct methanol fuel cells with both excellent oxygen reduction activity and methanol tolerance, hence electrodeposition of this alloy is an attractive approach for synthesizing porous metal electrodes with high methanol tolerance in direct methanol fuel cells. In this Study, we electrodeposited two types of Pd-Co films onto Au substrates by applying different Current density (-10 or -200 mA cm(-2)); and then characterized them in terms of morphology, composition, crystal structure, and catalytic activity. Pd-Co deposited at -10 mA cm(-2) was smooth and possessed smaller particles (ca. 10 nm), while that at -200 mA cm-2 was dendritic (or rough) and possessed larger particles (ca. 50 nm). Both the Pd-Co alloys were found to be almost the same Structure, i.e. a solid solution of ca. Pd7Co3 With Pd-skin, and also confirmed to possess comparable activity in oxygoen reduction to Pt (potential difference at 1.0 mu A cm(-2) was 0.05 V). As for methanol tolerance, cell-voltage was not influenced by addition of I mol dm(-3) methanol to the oxidant solution. Our approach provides fundamental technique for synthesizing Pd-Co porous metal electrodes by electrodeposition. (C) 2008 Elsevier Ltd. All rights reserved.

The effect of pH on the enantiospecificity of An (111) electrode modified with L-homocysteine was evaluated for the electrochemical redox reaction of 3,4-dihydroxyphenylalanine (DOPA). Cyclic voltammetric peaks clearly exhibited enantiospecificity at pH 0.6 and 2, whereas no enantiospecificity was observed at pH 3, 4, and 5.5. Scanning tunneling microscopy confirmed the highly ordered (2 root 3 x 3 root 3)R30 degrees structure of L-homocysteine at pH 0.6, at which L-homocysteine molecules form a dimer through the hydrogen-bond between carboxy groups (COOH), while a disordered structure was observed at pH 5.5. These results suggest that the dimer formed in the acidic solutions at pH below 3 plays an important role in providing the enantiospecificity to the Au(111) surface.

The feasibility of a di-block copolymer, composed of a polyethylene oxide (PEO) chain and a polystyrene (PS) chain covalently bonded, as the gel electrolyte for lithium secondary batteries was investigated. The PEO-PS di-block copolymer gel electrolyte showed a high ionic conductivity of similar to 1 mS/cm at room temperature. Moreover, it retained good mechanical strength within a co-continuous phase separated structure, and it suppressed the dendritic deposition of Li. Indications were that the interface between the electrolyte and the Li metal was chemically stable, as a result of the PEO phase fixed to PS by covalent bonding. In addition, it was indicated that the Li/PEOPS di-block copolymer gel electrolyte/LiFePO4 cell had a high charge-discharge efficiency of similar to 99% during 30 cycles, while maintaining a discharge capacity of 124 mAh/g.

Sheet-shaped carriers, having obverse and reverse surfaces and thus a large contact area as a targeting site, have several advantages over spherical-shaped carriers, which have an extremely small contact area. Herein is proposed a novel method for the preparation of free-standing nanoparticle-fused nanosheets having uniform micrometer shape, nanometer thickness and heterogenous surfaces, using a water-soluble sacrificial film. This was achieved by combination of four processes: (1) specific adsorption of latex beads at pH 5.0 and a concentration of 1.0 x 10(11) mL(-1) onto a patterned dodecyltrimethoxysilane self-assembled monolayer (DTS-SAM) region by a conventional dry patterning process, (2) fabrication of the latex bead-sheet via thermal-fusion at 110 degrees C for 60s, (3) preparation of the free-standing nanosheet by detachment from the DTS-SAM, and (4) hetero-modification of the resulting nanosheet using a water-soluble poly(acrylic acid) as a sacrificial supporting film. Thus, this sheet-shaped carrier having hetero-surfaces can be regarded as a new material for delivery of drugs, hemostatic reagents and as wound dressings for bum injury, etc. (C) 2007 Elsevier B.V. All rights reserved.

A simple numerical simulation of current flowing through electronic devices was examined for a hybrid power supply system composed of a DMFC and a capacitor connected in parallel. The simulation was investigated by representing a combination of ohmic resistance, charge transfer reaction resistance, mass transfer resistance and double layer capacitance of a DMFC as a simple ideal resistor, based on measured data when DMFC was generating electricity. The simulation result was found to agree with experimental measured current flowing through the DMFC and the capacitor, although a slight disagreement was observed because of the presence of ohmic resistance between circuit components. The simulation of DMFC-capacitor hybrid power supply system indicated the importance of the inner resistance of the capacitor. The hybrid simulation was also applied to a system assumed to consist of mu DMFC and micro electrochemical capacitor (MECC) system. The effect of applying a DC-DC converter to the system was indicated. The simulation allows to predict the degree of improvement required without performing actual fabrication of mu DMFC and MECC.

A wet process for forming an adhesive Cu layer on polyimide (PI) film was developed. In this process, the surface of the PI film is pretreated in plasma, followed by the formation of a ligand-bearing organic layer of 3-aminopropyl-triethoxy silane (APTES) molecules. After catalyzation with a solution containing Pd ions, thin layers of NiB as the underlayer and that of Cu as the conductive layer are deposited by electroless depositions, and then a 10 pm thick Cu layer is electrodeposited. The peel strength of the specimen prepared by this method was found to depend on the morphology of the NiB underlayer. A continuous NiB layer functions as a barrier layer that prevents Cu from contacting the PI film. In the presence of this efficient barrier layer, the peel strength was found to improve after annealing at 150 degrees C.

Magnetic properties of [ Tb20Co80/Pd(0.8 nm)](20) multilayered films with a TbCo layer of thickness 0.2-8.0 nm were studied using spectroscopic techniques of soft x-ray absorption (XAS) and magnetic circular dichroism ( MCD) at the Co L-2,L-3 and Tb M-4,M-5 edges. The compensation layer thickness of TbCo, where magnetization becomes zero, was observed to be 5-6 nm. XAS and MCD analyses using the sum rule revealed that the existence of the compensation layer thickness was primarily because the projected Tb 4f magnetic moment was enhanced with the increase in the layer thickness, while the Co 3d moment was independent of the layer thickness. Below the compensation layer thickness, Co sublattice magnetization was dominant.

A mesoporous Sn anode was electrodeposited in the presence of lyotropic liquid crystals made of nonionic surfactants. The introduction of mesoporous structure was effective for the accommodation of volume change of Sn during charge and discharge cycling of Li ions. The discharge capacity of the mesoporous Sn anode at 1 C rate was as high as 425 mA h g(-1) at the 100th cycle, and that was as high as 320 mA It g(-1) at the 100th cycle even though at 5 degrees C rate.

Synthesis of An nanoparticles (NPs) and their immobilization on optical waveguide (OWG) made of quartz plate were carried out aiming at application to sensing. Au NPs with diameters of similar to 5 nm and similar to 20 nm were synthesized by reduction of tetrachloroaurate ions with borohydride and immobilized on quartz OWG coated with monolayer of organosilane. With the OWG spectroscopy, the surface plasmon absorption of the An NPs immobilized on OWG was suggested to be influenced by the particle size and the interparticle distance and to response to the refractive index of nanoparticle proximity sensitively. (C) 2007 Elsevier B.V. All rights reserved.

In lithium ion batteries, it has previously been shown that Ni-Sn thin film anodes containing 62 at.% Sn show outstanding electrochemical characteristics, e. g. good capacity and endurance, during charge-discharge cycling. However, their mechanical response, which is likely related to their lifetime in service, has so far received relatively little attention. To address this, nanoindentation and nanowear techniques have been used to characterize the mechanical properties of thin Ni-Sn films electrodeposited on a copper substrate. In situ morphology analysis together with in situ stress measurement has been performed to assess the properties of Ni-Sn thin film anodes during electrochemical cycling. The change in mechanical properties, residual stress and fracture behaviour of the anodes is related to the phase changes which occur during charge-discharge cycling. The correlation between the mechanical properties of the films and their charge-discharge characteristics serves as a useful indicator for optimized design of a Sn-based intermetallic anode film for lithium ion secondary batteries.

Nanoparticles of Pd-Sn were prepared under various conditions by applying ultrasonic irradiation. The Pd-Sn nanoparticles thus prepared were about 3-5 nm in diameter. The Pd in Pd-Sn nanoparticles was found to be mostly in the metallic state. The PdSn nanoparticles have a better oxygen reduction reaction (ORR) activity than Pt and Pd nanoparticles in alkaline media. The mole ratio of Pd to Sn metal ions, their initial concentrations, the amount of ethanol, which served as the reducing agent for metal ions, and the amount of citric acid in the synthesizing solution were found to affect the size and distribution of obtained Pd-Sn nanoparticles. Therefore, the electrocatalytic activity for oxygen reduction was controlled by the above factors. Particularly, the amount of citric acid is important to control the surface modification on Pd-Sn particles to adjust the electrocatalytic activity for oxygen reduction. ©The Electrochemical Society.

Herein we firstly reported the effects of generation 5 polyamidoamine dendrimerfunctionalized fluorescent multi-walled carbon nanotubes(dMNTs) on mice embryonic stem cell line CCE. The dMNTs were prepared and characterized, and incubated with murine ES CCE cells for 1 to 5day. These ES cells were observed by fluorescent microscopy, and were analyzed by flow cytometer and MTT. Results showed that the dendrimer-functionalized fluorescent multi-walled carbon nanotubes were successfully synthesized, could enter into ES cells quickly, more than 20μg/ml dose caused ES cells become smaller and smaller as the incubation time increased, and inhibited cell growth in dose- and time-dependent means, less than 5 μg/ml dose improves ES differentiation. These results demonstrate that dMNTs are toxic to ES cells at large dose, can induce ES cells' differentiation at small dose. The prepared dMNTs may be a highly efficient gene delivery system for ES cells, have potential applications in ES research. © The Electrochemical Society.

Polyether chains have been successfully grafted onto the interlayer surface of a Dion - Jacobson- type layered perovskite, HLaNb2O7 center dot xH(2)O, by a reaction between an n- decoxy- derivative of HLaNb2O7 center dot xH(2)O and CH3(OCH2CH2)(m)OH (1 <= m <= 4). After the reaction, the interlayer distance decreases from 2.73 nm to 1.58 (m = 1), 2.07 (m = 2), 2.28 (m = 3), and 2.69 (m = 4) nm. Solid- state C-13 CP/MAS NMR spectroscopy indicates that the CH3(OCH2CH2)(m)O-groups are bound to the interlayer surface of HLaNb2O7 center dot xH(2)O. The n- decoxy groups are completely removed by the reaction with CH3(OCH2CH2) mOH (m = 2 and 3), while a part of the n- decoxy groups remain after the reaction with CH3(OCH2CH2)(m)OH (m = 1 and 4). Upon treatment of the CH3(OCH2CH2)(m)O-grafted HLaNb2O7 center dot xH(2)O (m = 2 or 3) with a CH3(OCH2CH2) mOH solution of LiClO4, the interlayer distance decreases further to 1.78 (m = 2) and 2.01 (m = 3) nm. Inductively coupled plasma emission spectrometry reveals the presence of lithium (0.22 (m = 2) and 0.24 (m = 3) per [LaNb2O7]). The presence of ClO4- ions is demonstrated by Raman spectroscopy, and the position of the nu(1)(A(1)) band indicates the presence of isolated ClO4- ions in the interlayer space. After treatment with a LiClO4 solution, CH3(OCH2CH2)(m)O-grafted HLaNb2O7 center dot xH(2)O (m = 2 and 3) exhibits ionic conductivity, and no clear temperature dependence is observed.

An organic molecular sensor with a plasmon antenna was developed. A coaxial Ag grating antenna was designed by a finite differential time domain (FDTD) calculation and fabricated by a lift-off process. When pumping light was irradiated onto the sensor, a surface plasmon wave was generated and focused at the center of the antenna
this wave produced a strong electric field. By coating a cystamine self-assembled monolayer (SAM) onto the sensor, strong Raman scattering light produced by a surface-enhanced Raman scattering (SERS) effect was observed at the center of the device. The Raman spectrum showed good agreement with that of cystamine on a Ag surface. The Raman intensity at the center of the device increased significantly and was more than 2,000 times that outside the device. Our optical sensor can detect an unknown single molecule and can be incorporated into other sensors such as gas sensors and biosensors. © The Electrochemical Society.

The purpose of this work was to study the effect of surface morphology on the responses to pH and ionic strength of a SiO2/Si reference electrode (RE) modified by octadecyltrimethoxysilane (ODMS). Representative REs with contact angles (CA) of 60°, 80° and 106° were studied in various solutions: those with combined effects of pH and ionic strength, those with ionic strength variation and constant pH, and those with pH variation and constant ionic strength. REs with the flat surface show response to ionic strength, while REs with the rough surface show response to pH. The reason may be that total ionic strength determines the charge and potential distribution in the electrolyte-insulator-semiconductor structure for REs with flat surfaces, but that the combined effects of uncovered binding sites, penetration of H + into pinholes, and the special adsorption of H+ dictate the charge and potential distribution for REs with rough surfaces. © The Electrochemical Society.

This paper reviews important research on chemical and electrochemical synthesis and application of nanoparticles, especially our recent results in this field: (i) catalytic metal nanoparticles for micro-fuel cells. (ii) magnetic oxide nanoparticles for drug delivery systems, and (iii) magnetic metal nanoparticles for magnetic recording media. To fulfill the requirements of each application, we chose and modified those synthetic methods for obtaining suitable properties, e.g., morphology, catalytic activity, and magnetic properties. (i) For micro-fuel cells, electrodeposition is attractive because of its selective deposition onto Current collectors and possible elimination of an annealing process. As a result, we have successfully synthesized Pt, PtRu alloy, and PdCo alloy, which consisted of dendritic structures macroscopically and of interconnected nanoparticles microscopically. (ii) For drug delivery systems, since magnetic nanoparticles should possess ferromagnetism, be dispersible in water, and be nontoxic, Fe3O4 nanoparticles synthesized by hydrolysis in aqueous media are suitable. As a result, we have successfully controlled the size (10-40 nm in diameter) and the magnetic properties of Fe3O4 nanoparticles by means of adjusting the molar ratio of ferrous to ferric ions in the precursor Solution. (iii) For magnetic recording materials, since magnetic nanoparticles should possess high coercivity, a controlled shape, and a uniform small size, we have modified a chemical method for synthesizing FePt by adjusting the growth temperature. As a result, we have succeeded in synthesizing FePt nanoparticles with a controlled shape (Cubic) and a uniform size (ca. 5.6 nm).

Nanoparticles of Pd-Sn were prepared under various conditions by applying ultrasonic irradiation. The Pd-Sn nanoparticles thus prepared were about 3-5 nm in diameter. The Pd in Pd-Sn nanoparticles was found to be mostly in the metallic state. The PdSn nanoparticles have a better oxygen reduction reaction (ORR) activity than Pt and Pd nanoparticles in alkaline media. The mole ratio of Pd to Sn metal ions, their initial concentrations, the amount of ethanol, which served as the reducing agent for metal ions, and the amount of citric acid in the synthesizing solution were found to affect the size and distribution of obtained Pd-Sn nanoparticles. Therefore, the electrocatalytic activity for oxygen reduction was controlled by the above factors. Particularly, the amount of citric acid is important to control the surface modification on Pd-Sn particles to adjust the electrocatalytic activity for oxygen reduction. ©The Electrochemical Society.

We demonstrate the magnetically induced orientation of mesochannels in mesoporous silica films prepared with low-molecular-weight surfactants under an extremely high magnetic field of 30 T. This process is principally applicable to any type of surfactant that has magnetic anisotropy because such a high magnetic field provides sufficient magnetic energy for smooth magnetic orientation. Hexadecyltrimethylammonium bromide (CTAB) and polyoxyethylene-10-cetyl ether (Brij 56) were used as cationic and nonionic surfactants, respectively. According to XRD and cross-sectional TEM, mesochannels aligned perpendicular to the substrates were observed in films prepared with low-molecular-weight surfactants, although the effect was incomplete. The evolution of these types of films should lead to future applications such as highly sensitive chemical sensors and selective separation.

Nanostructured Pt particles are directly deposited onto a Ni foam by utilizing displacement plating after a lyotropic liquid crystalline phase including Pt species was prepared within macropores of the Ni foam. The EDS mapping of Pt after deposition corresponds to the macroscopic framework of the Ni foam, indicating the uniform displacement plating of Pt on the surface of the Ni foam. The Pt particles of 150-250 nm in size are formed over the entire area of the surface of the Ni foam. The TEM images prove that the nanoscale rods (width: about 3 nm) are aggregated with each other to form nanoscale porosity. The active area of Pt can be estimated to be ca. 12 m(2)/g by using the cyclic voltammogram in sulfuric acid. Our method realizes one-step production of hierarchical macro-meso type porous electrodes. (c) 2007 Elsevier Ltd. All rights reserved.

A CoNiFeB soft magnetic thin film with high saturation magnetic flux density (B-s) for use as a magnetic recording head core material or as a soft magnetic underlayer of a double perpendicular magnetic recording medium was prepared by electroless deposition. When the CoNiFeB alloy thin film was deposited on a evaporated Cu (100 nm thick)/glass substrate, the saturated magnetic flux density was found to increase up to 2.0 T by increasing the concentration of FeSO4, The coercivity (H-c) was found to decrease to 6 Oe while the saturated magnetic flux density was maintained higher than 1.8 T by optimizing the concentrations of tartaric acid and citric acid in the electroless plating solution. An X-ray diffraction (XRD) study showed that the intensity of the assigned peak in the bee (1 1 0) of CoNiFeB film decreased as the concentration of tartaric acid was decreased. Moreover, the coercivity of the CoNiFeB film formed on a NiFe substrate exhibits lower coercivity than that formed on a Cu substrate. (c) 2007 Elsevier Ltd. All rights reserved.

This review describes our recent works on the preparation of Ni-alloy films deposited by electroless deposition as a diffusion barrier layer for ultra large-scale integration (ULSI) interconnects by using an all-wet process. In this process, we create a novel wet fabrication process including a self-assembled monolayer (SAM) as an attachment technique between diffusion barrier layer and a substrate. Our proposal process was applied to the substrates Of SiO2/Si and both organic (methyl silsesquioxane) and inorganic (hydrogen silsesquioxane) low-k dielectrics. The key technique of this proposed process is using SAM as a catalyst trapping layer. The Ni-alloy films such as NiB were deposited on catalyzed SiO2 or low-k substrates. The electrolessly deposited NiB films were found to exhibit sufficient thermal stability and an acceptable barrier property for preventing Cu diffusion into the SiO2 and low-k dielectrics. (c) 2007 Elsevier Ltd. All rights reserved.

The process for electroplating amorphous gold-nickel-tungsten alloy that we developed previously based on the addition of a gold salt to a known amorphous Ni-W electroplating solution was investigated further using the X-ray diffraction (XRD) method for the purpose of quickly surveying the effects of various experimental variables on the microstructure of the alloy. In this system the gold concentration in the plating bath was found to be critical; i.e., when it is either very low or very high, the deposit becomes crystalline to XRD. The deposit composition varies linearly with the mole ratio of An to Ni in solution, and the alloy deposit is amorphous to XRD when the atomic ratio of Au/Ni in the deposit is between 0.5 and 1.5. At suitable concentrations of the metal ions, the deposit contains essentially no tungsten. By extending the work on the Au-Ni-W system, an amorphous Au-Co alloy plating process was also developed. (C) 2007 Elsevier Ltd. All rights reserved.

We have carried out X-ray absorption measurements with its magnetic circular dichroism (MCD) of perpendicular magnetic films of DyxCo100-x (15 <= x <= 33) at Dy M-4,M-5 and Co L-2,L-3 absorption edges to investigate electronic and spin states of the Dy 4f and Co 3d states, respectively. The replacement of major spin between Dy 4f and Co3d is clearly observed in the spectra between 20 <= x <= 25. The expected values of the orbital angular moment vertical bar < L-z >vertical bar of Dy 4f were estimated to be 1.4-0.8 mu(B) while that of Co 3d was estimated to be around 0.2 mu(B). (c) 2007 Elsevier Ltd. All rights reserved.

Nanoparticles of Fe3O4 were synthesized by hydrolysis in an aqueous solution containing ferrous and ferric salts at various ratios with 1,6-hexanediamine as a base. It was found that the ferrous to ferric ratio influences the reaction mechanism for the formation of Fe3O4. When the ratio of ferrous to ferric ions was increased, the formation of large hydroxide particles as a precursor of Fe3O4 was promoted, which resulted in an increase in the size of Fe3O4 nanoparticles. As a result, the mean diameter of Fe3O4 nanoparticles increased from similar to 9 to similar to 37 nm as the molar percentage of ferrous ions with respect to the total iron ions was increased from 33 to 100%. Furthermore, it was demonstrated that magnetic properties of Fe3O4 nanoparticles can be controlled by adjusting the molar ratio of ferrous to ferric ions as well as the particle diameter. (C) 2007 Elsevier Inc. All rights reserved.

Nanoparticles of Fe(3)O(4) were synthesized by hydrolysis in an aqueous solution containing ferrous and ferric salts at various ratios with 1,6-hexanediamine as a base. It was found that the ferrous to ferric ratio influences the reaction mechanism for the formation of Fe(3)O(4). When the ratio of ferrous to ferric ions was increased, the formation of large hydroxide particles as a precursor of Fe(3)O(4) was promoted, which resulted in an increase in the size of Fe(3)O(4) nanoparticles. As a result, the mean diameter of Fe(3)O(4) nanoparticles increased from approximately 9 to approximately 37 nm as the molar percentage of ferrous ions with respect to the total iron ions was increased from 33 to 100%. Furthermore, it was demonstrated that magnetic properties of Fe(3)O(4) nanoparticles can be controlled by adjusting the molar ratio of ferrous to ferric ions as well as the particle diameter.

We fabricated SmCo5 double-layered perpendicular magnetic recording media with high perpendicular magnetic anisotropy for realizing ultra high density recording. A double-layered medium with a Ru buffer layer introduced between a Cu/Ti intermediate layer and a Co-Zr-Nb soft magnetic underlayer exhibited high perpendicular magnetic anisotropy, whereas that without the Ru buffer layer did not. Auger electron spectroscopy revealed that the Ru buffer layer inhibited interdiffusion between the Cu/Ti intermediate layer and the Co-Zr-Nb soft magnetic underlayer. We report here for the first time the read-write characteristics of SmCo5 double-layered perpendicular magnetic recording media. The medium noise was small in the medium with a Sm-Co layer deposited under high Ar gas pressure owing to small magnetic clusters.

The enantioselectivity imparted to a gold electrode by modifying its surface with a self-assembled monolayer (SAM) of cysteine (Cys) was investigated for the electrochemical redox reaction of 3,4-dihydroxyphenylalanine (DOPA). A cyclic voltammetric study of the redox reaction revealed that the enantioselectivity was determined by the surface coverage of the gold electrode with Cys molecules. The electrode modified with approximately 1.8 x 10(14) Cys molecules cm(-2) exhibited enantioselectivity in the voltammogram for the oxidation and reduction of DOPA, while the voltammograms obtained by the electrodes with either more or less surface coverages did not exhibit significant enantioselectivity. It is suggested that the accessibility of DOPA to that area of the gold surface which is not blocked by Cys molecules at an optimum surface coverage, is required for the enantioselective redox reaction of DOPA to proceed.

Different shapes (nanosphere or nanorod) of gold nanoparticles (Au-NPs) were synthesized with and without ultrasonic irradiation in the presence of citric acid. Spherical-shaped and rod-shaped Au-NPs showed different surface plasmon resonance (SPR) absorption bands. The Au-NRs with different shapes were immobilized on a monolayer of 3-aminopropyltriethoxysilane (APS) coated on an indium-tin oxide (ITO) electrode. The potential dependence of the SPR band of different shaped Au-NPs in an aqueous solution was explored. The SPR band and intensity changes of the Au-NPs were found to depend on the applied potential. The spherical-shaped and rod-shaped Au-NPs showed different SPR absorption behaviors when potential was applied. These behavior changes were interpreted as the result of the potential-induced changes of the local dielectric environment around the nanoparticles due to molecular absorption/desorption and the charging/discharging of the particles. (C) 2007 Elsevier Ltd. All rights reserved.

An extremely enhanced enantioselectivity was achieved for the detection of enantiomers of alanine (Ala), leucine (Leu), and 3,4-dihydroxyphenylalanine (DOPA) based on the voltammograms for the deposition of Cu from Cu complexes of the amino acids at an Au electrode modified with a self-assembled monolayer (SAM) Of L-homocysteine (Hcy). The enantioselective current density peak for the Cu deposition was found to change with increasing number of potential cycles after the addition of Cu(II), and the highest enantioselectivity was observed immediately after the addition of Cu(II). Besides, enantio selectivity was not observed with proline, whose five-membered ring contains the nitrogen atom of a secondary amino group, while some amino acids with a primary amine group such as Ala, Leu, and DOPA exhibited enantioselectivity. These results suggest that the chiral ligand exchange reaction at the L-Hcy SAM-modified Au electrode, namely, the enantioselective formation of diastereomeric complexes of Cu(II) with target enantiomers and L-Hcy self-assembled on the Au electrode, plays an important role in the chiral discrimination based on the Cu deposition. (c) 2006 Elsevier B.V. All rights reserved.

The filling of trenches in ULSI interconnect structure by electroless copper deposition was investigated for the effect of bath additives. The additive effect was found to depend strongly on the reducing agent used in the bath. Void-free trench-filling was achieved by using polyethylene glycol (PEG) as an inhibiting additive in the bath containing glyoxylic acid as the reducing agent, while the combined addition of 8-hydroxy-7-iodo-5-quinoline sulfonic acid (HIQSA) and PEG was necessary for achieving void-free filling in the bath containing formaldehyde as the reducing agent. The effect of PEG on trench filling in the former bath was studied in detail based on electrochemical measurements. It is suggested that the rinse water remaining in trenches before electroless deposition causes a decrease in PEG concentration at the trench bottom during copper filling. The addition of PEG was found to shift the deposition potential in the negative direction. A new potential measuring apparatus was devised and used in model experiments, which revealed that the deposition potential depends on the local concentration of PEG at the trench bottom, where it is expected to be low. The observed preferential growth of copper deposit at the trench bottom is thus attributed to the effects of the variation of PEG concentration within the trenches on the deposition rate and potential.

Void-free copper filling of trenches for ultralarge scale integrated interconnect structure was demonstrated by electroless deposition technique using polyethylene glycol as an inhibiting bath additive. With this electroless plating bath, the authors succeeded in demonstrating superfilling. Of particular interest is that the deposition at trench opening was nil during the filling process, while that at the bottom was very fast. This letter presents a demonstration and a proof of superfilling of trenches by electroless copper deposition. (c) 2007 American Institute of Physics.

Our recent study on a challenge of new materials for next generation's magnetic recording approaching an ultra high areal recording density beyond 1 Tbit/in.(2) is overviewed. We proposed novel methods for fabricating high performance magnetic recording heads and media by making the best use of wet (electro- and electroless-deposition) and dry (sputtering) processes. We believe that these results contribute significantly to the progress in magnetic recording and constitute a breakthrough for materializing an unexplored areal recording density beyond I Tbit/in.2. (c) 2006 Elsevier Ltd. All rights reserved.

The use of self assembly monolayer has been demonstrated for direct plating on interlevel dielectric for interconnects applications. In this work we show an additional feature of that technique for direct deposition on contact application. We also present an integrated process where the self assembly activation is used for both the deposition of the barrier layer which can be used for both the contact material and the source for the silicidation process. Later all wet electroless process can be used for the contact buildup and the capping layer deposition. In this work we review the depositions of electroless Nickel alloy on various inter level dielectrics and on Si. We also discuss the integration process including deposition on exiting silicide or possible self silicidation for the formation of self aligned NiSi. We describe the process outlines and present material and electrical properties.

Sputter-deposited SmCos thin films exhibiting high perpendicular magnetic anisotropy were studied for materializing ultra high density magnetic recording. This study put emphasis on the fabrication of SmCos double-layered perpendicular magnetic recording media. A double-layered medium with a Ru buffer layer introduced between a Cu/Ti intermediate layer and a Co-Zr-Nb soft magnetic underlayer exhibited high perpendicular magnetic anisotropy, whereas that without the Ru buffer layer did not. Auger electron spectroscopy revealed that the Ru buffer layer inhibited unfavorable interdiffusion between the Cu/Ti intermediate layer and the Co-Zr-Nb soft magnetic underlayer. In addition, the readwrite characteristics of the SmCos double-layered perpendicular magnetic recording media were evaluated for the first time. copyright The Electrochemical Society.

DAAQ(1,5-diaminoanthraquinone)/MWCNT composites were prepared by chemical polymerization of DAAQ onto MWCNT and their capacitance was evaluated by means of cyclic voltammetry and charge-discharge cycling in 1M H2SO 4 electrolyte. The performances of such cells have been compared with pure MWCNT and DAAQ based electrodes. The SEM image shows that DAAQ was coated onto MWCNT during polymerization. The highest specific capacitance values of 210 F/g were observed. DAAQ/MWCNT composites also showed long cyclic stability in charge-discharge test. copyright The Electrochemical Society.

We have investigated the effects of the etching method of a Ti substrate for a metal oxide electrode on the electrochemical characteristics of the electrode. The preparation method and electrochemical characterization of zirconium oxide films on etched Ti substrate has been also studied. The HCl etching was developed a fine and homogeneous roughness on the Ti substrate. Fabrication and material properties of the metal oxide electrode, which is known to be so effective to generate ozone and sodium hypochlorite (NaOCI) as power oxidant, were studied. A proper metal oxide material focus zirconium oxide through reference paper. A coating method to enhance the fabrication reproducibility of the zirconium oxide electrode was used dip-coating method by zirconium oxychloride. Zirconium oxide films on the Ti substrate were analyzed by SEM, XPS and cyclic voltaminetry. (C) 2007 Elsevier Ltd. All rights reserved.

The stress of the electrodeposited pure Sn and the Ni-62 atom % Sn alloy thin film electrodes during cycling was measured in situ using an optical cantilever method. The results revealed that the Ni-62 atom % Sn alloy electrode with better cycle endurance actually experiences larger stress compared to the pure Sn electrode. Furthermore, the stress-release phenomenon during the open-circuit period has been confirmed for the first time. This paper demonstrates that the cantilever bending method is effective for the in situ study of the stress development, transition, and hence the phenomena taking place within the Sn-based electrodes. (c) 2007 The Electrochemical Society.

An impedance analysis method for the catalyst layers of a direct methanol fuel cell is evaluated through demonstrating analyses and comparison of two types of the catalyst layers. The catalyst layers were prepared with different dispersing solvents: ethyleneglycol dimethyl ether or isopropyl alcohol aqueous solution. Methanol oxidation current of the catalyst layer prepared with the former solvent was more than twice that with the latter. The proposed method was revealed to have the potential for analyzing the difference clearly in terms of parameters, using our transmission-line equivalent circuit for the catalyst layers based on the assumption of primary and secondary pores. The parameters indicate that the main drawback of the catalyst layer prepared with the latter solvent is 85 times larger ionic resistance in the secondary pores. Moreover, precise analyses on the parameters indicate the microstructures of the catalyst layers, which correspond to a model reported previously. We conclude that this method is effective in analyzing the catalyst layer of the fuel cell. (C) 2007 The Electrochemical Society.

Fundamental electronic properties of methyl-modified n-Si(111) interfaces created by the displacement of Cl on Si(111) surface by the methyl group from Grignard reagents (RMgX; X=Br or Cl, R = methyl) were measured in the presence and absence of water. The presence of water played a significant role in determining the behavior of the devices. The structure of Ga-In/methyl monolayer/n-Si(111) was not rectifying but only consisted of series resistances. On the other hand, a diode-like rectifying property was observed with the water/methyl layers/n-Si(111) heterojunction structure. Functionalization of Si(111) surfaces with various alkyl moieties such as methyl, ethyl, propyl, butyl, and mixed methyl/propyl, was studied by electrochemical measurements performed in a mixture of 3 mM K3Fe(CN)(6)/3 mM K4Fe(CN)(6)/1 MKCl/H2O and by surface characterization with synchrotron radiation X-ray photoelectron spectroscopy. The transistor characteristics of field effect transistor-like devices with water/alkyl/n-Si(111) gate structures were investigated. The device properties clearly depended on the alkyl moiety: transistor-like behavior was observed only for devices with methyl moiety, and for those with a mixed methyl-propyl monolayer prepared by using Grignard reagents with mixed methyl and propyl (CH3MgBr:CH3CH2CH2MgBr=1:9) moieties, whereas no transistor-like behavior was observed for devices with butyl or ethyl moiety. (c) 2007 The Electrochemical Society.

Pd-Co was electrodeposited as a rough cathode catalyst for a direct methanol fuel cell fabricated using micro-electromechanical systems technology. Pd-Co was electrodeposited at -10 mA/cm2 for 60 s or -200 mA/cm 2 for 5 s. The deposits were evaluated with respect to microstructures, electrochemical characteristics, and fuel cell performances. As a result, oxygen reduction activity of the sample prepared at -200 mA/cm 2 was higher than that prepared at 10 mA/cm , while the electrochemically active surface areas were almost the same. Microstructures of the former and the latter were observed dendritic and flat, respectively. We conclude that the difference of oxygen reduction activity is attributed to the difference of the microstructure. In addition, we modified the dendritic sample by depositing Pd-Co at -0.75 V vs. Ag/AgCl. The modification increased open circuit potential for oxygen reduction by 30 mV from 0.70 to 0.73 V. ©The Electrochemical Society.

A wet process based on electroless deposition is proposed for the formation of a diffusion barrier layer for Cu wiring in ultra-large scale integration (ULSI) technology. The diffusion barrier layer is formed on a low-dielectric constant (low-k) inter level film. In this process, a Pd-activated self-assembled monolayer as a seed/adhesion layer was used as a key step to allow electroless deposition on a dielectric film. The effectiveness of this approach was demonstrated by depositing an electroless NiB layer as the diffusion barrier layer. The electrolessly deposited NiB layer showed a uniform surface, a small grain size, and a high adhesion when deposited on various common inter level dielectric materials with low dielectric constant. The electrolessly deposited NiB layer formed on the low-k dielectric film by this method showed a high thermal stability of the effectiveness as a barrier to Cu diffusion at temperatures up to 400 degrees C for 30 min. The electroless process was found to be reproducible and did not affect dielectric properties of the underlying insulator. (c) 2007 The Electrochemical Society.

Structural and energetic investigations based on semiempirical PM5 and ab initio HF and MP2 calculations suggested that the self-assembled monolayer of an atropisomeric compound, (R)- or (S)-1,1'-binaphthalene-2,2'-dithiol (BNSH), on a gold (1 1 1) surface selectively adsorbs one enantiomer of phenylalanine (Phe), resulting in chiral discrimination, through hydrophobic, cation(-NH3+)-pi and NH(Phe)-pi (BNSH) interactions in a nanometer-sized screw-hole-like pocket composed of three BNSH molecules in the monolayer. (c) 2006 Elsevier B.V. All rights reserved.

The enantioselectivity of the self-assembled monolayer (SAM) of homocysteine formed on the (111)-oriented gold surface was investigated. We analyzed the redox behavior of 3,4-dihydroxyphenylalanine (DOPA), which is an electrochemically active chiral molecule, by means of cyclic voltammetry at a gold electrode modified with one enantiomeric form of homocysteine. It was demonstrated that the homocysteine SAM of one enantiomeric form blocked the redox reaction of only one enantiomer of DOPA, with cross inversion for the other enantiomer, in acidic solution.

The chemical reduction of ferrous or ferric ions to metallic iron by a reducing agent such as sodium borohydride (NaBH4), hydrazine (N2H4), or sodium phosphonate (NaH2PO2) and its subsequent oxidation were investigated for the preparation of iron-oxide nanoparticles in reverse micelles. The crystal structure and crystallinity of the oxide nanoparticles were found to depend on the oxidation potential of the reducing agent and the catalytic activity of the surface of deposited iron. In addition, it was demonstrated that the process used for oxidizing the metallic iron was critical for the formation of oxide nanoparticles, and that the enhancement of magnetic properties was achieved by providing a flow of oxygen during the oxidation process. (c) 2006 Elsevier Ltd. All rights reserved.

High-efficientcy micro-electrochemical devices are realized by increasing electrode surface areas while maintaining keeping chip size. The use of three dimensional (3-D) electrodes instead of planar electrodes is effective for this purpose. To realize a metal pattern on 3-D structures, spray coating was utilized and the optimum condition for achieving a good photoresist step coverage was determined. A good step coverage of the photoresist was obtained on the obtuse corner formed by the anisotropic wet etching of (100) silicon and even on the vertical corner formed,by deep reactive ion etching (RIE). We applied this method to fabricate a high-performance micro direct methanol fuel cell (mu DMFC). An open circuit voltage of 548 mV and a maximum power density of 0.72 mW/cm(2) were obtained at room temperature with 2 M methanol.

LiNi1/3Mn1/3Co1/3O2 had been successfully prepared from spherical composite carbonate via a simple uniform-phase precipitation method [P. He, H. Wang, L. Qi, T. Osaka, J. Power Sources, in press] at normal pressure, using nickel, cobalt and manganese sulfate and ammonia bicarbonate as reactants. The preparation of spherical composite carbonate was significantly dependant on synthetic condition, such as the reaction temperature, feed rate, molar ratio of these reactants, etc. The optimized condition resulted in spherical composite carbonate of which the particle size distribution was uniform, as observed by scanning electronic microscopy (SEM). Calcination of the uniform composite carbonate with lithium carbonate at high temperature led to a well-ordered layer structured LiNi1/3Mn1/3Co1/3O2 as confirmed by X-ray diffraction (XRD), without obvious change in shape. Due to the homogeneity of the composite carbonate, the final product, LiNi1/3Mn1/3Co1/3O2, was also significantly uniform, i.e., the average particle size was of about 10 mu m in diameter and the distribution was relatively narrow. As a result, the corresponding tap density was also high, approximately 2.32 g cm(-3), of which the value is very near to that of commercialized LiCoO2. In the voltage range of 2.8-4.2, 2.8-1.35 and 2.8-4.5 V the discharge capacities of LiNi1/3Mn1/3Co1/3O2 electrode were 159, 168 and 179 mAh g(-1), respectively, with good cyclability. (c) 2006 Published by Elsevier B.V.

Pd nanocluster seeds were formed on a soft magnetic underlayer (SUL) using an electrochemical substitution reaction, and were utilized as an intermediate layer for a Co/Pd multilayered ([Co/Pd](n)) perpendicular magnetic recording medium. A CoNiFeB film prepared with electroless deposition was used as SUL, which was immersed into a PdCl2 solution for the formation of Pd seeds. The Pd seeds were found to effectively reduce the size of magnetic domains in the [Co/Pd](n) film deposited on them. The optimization of the concentration of the PdCl2 solution and the use of the pretreatment process with a SnCl2 solution were effective to obtain the smooth SUL surface with fine Pd seeds as small as 5 nm. The 20 nm-thick [Co/Pd] n film deposited on the optimized Pd seeds/CoNiFeB SUL exhibited a high coercivity of 7.8 kOe and a small magnetic domain size of 69 nm. These results indicated that the combination of the Pd seeds and the electroless-deposited SUL was desirable in terms of the improvement not only in the magnetic properties of [Co/Pd] n media but also in the mass productivity of the underlayer. (C) 2006 Elsevier B.V. All rights reserved.

Crystallization of chiral amino acid, leucine, on the gold substrate modified with a self-assembled monolayer (SAM) was investigated with X-ray diffraction (XRD) and atomic force microscopy (AFM). It was found that the formation of enantiomeric crystalline phase occurred enantioselectively when the specimen modified with the SAM, to which one enantiomeric form of leucine molecules was covalently attached, was immersed in a pure enantiomeric solution of leucine. On the contrary, a racemic crystalline phase was formed on both D- and L-leucine-attached SAMs after soaking in a racemic leucine solution. In non-racemic solutions, both enantiomeric and racemic crystalline phases were formed on the enantiomer-attached SAM when the one enantiomeric form with the same chirality as the attached enantiomer was contained in excess, while neither of the crystals was formed with the other enantiomeric form in excess. Changes in the surface morphology of the specimens accompanied with the growth of crystalline phases on the SAM, reflecting the crystallinity suggested from the XRD method, were observed by using AFM. (c) 2006 Elsevier B.V. All rights reserved.

The soft x-ray absorption and magnetic circular dichroism spectra at the Co L-2,L-3-edges of [Co/Pd](20) and [CoB/Pd](20) multilayered films, which were sputter- deposited in Ar gas containing N-2 at room temperature, were measured to investigate the electronic and spin states of the films. The macroscopic magnetic properties, such as coercivity and saturation magnetization, and microstructural properties, such as grain size and preferred orientation, were markedly changed for the [Co/Pd](20) film by the B doping and N-2 addition. The B doping and/or the addition of N-2 gas caused appreciable changes not only in macroscopic magnetic properties but also in microscopic properties, such as the spin angular momentum and orbital angular momentum, throughout the multilayered film. On the other hand, a new spectral feature at the high energy side of the Co L-3-edge peak in x-ray absorption spectra was found in only the films with N-2 added. Thus, the microscopic properties, such as electronic and spin states, of the Co 3d electronic state for the [Co/Pd](20) and [CoB/Pd](20) films were changed by only the sputtering process with additive N-2 gas.

LiCoO2 had been successfully prepared from spherical basic cobalt carbonate via a simple uniform-phase precipitation method at normal pressure, using cobalt sulfate and urea as the reactants. The preparation of spherical basic cobalt carbonate was significantly dependant on synthetic condition, such as the reactant concentration, reaction temperature and impeller speed, etc. The optimized condition resulted in spherical basic cobalt carbonate with uniform particle size distribution, as observed by scanning electron microscopy. Calcination of the uniform basic cobalt carbonate with lithium carbonate at high temperature led to a well-ordered layer-structured LiCoO2 without shape change, as confirmed by X-ray diffraction. Due to the homogeneity of the basic cobalt carbonate, the final product, LiCoO2, was also significantly uniform, i.e., the average particle size was of about 10 mu m in diameter and the distribution was relatively narrow. As a result, the corresponding tap-density was also high approximately 2.60 g cm(-3), of which the value is higher than that of commercialized LiCoO2 of Hunan Ruixing, co. In the voltage range 2.8-4.2, 2.8-4.3, and 2.8-4.4 V, the discharge capacities of LiCoO2 electrode were 153, 159, and 168 mAh g(-1), respectively, with better cyclability. (c) 2005 Elsevier B.V. All rights reserved.

We have developed an excellent process for selective deposition of mesoporous Pt through tailored microfabrication steps via the "Solvent-Evaporation-mediated Direct Physical Casting (SEDPC)" method. The direct observation by high-resolution scanning microscopy (HR-SEM) shows the formation of an ordered mesoporous structure in a very confined area. The cyclic voltammogram of the mesoporous Pt reveals a typical feature of Pt surface. The surface morphology and ordering of the mesostructure strongly depend on the electrodeposition conditions (constant-current and constant-potential depositions). The roughness factors are greatly enhanced as the charge densities in the constant-current deposition are increased. These findings are important for the morphological design of mesoporous metals in a micrometer scale. (c) 2006 NIMS and Elsevier Ltd. All rights reserved.

This article reviews results of our investigations, performed over the period of a decade, on gold plating for electronics applications. Three different topics are covered: (1) development of a new, non-cyanide, soft-gold electroplating bath containing both thiosulfate and sulfite as ligands; (2) evaluation of a known cyanide-based, substrate-catalyzed electroless bath for depositing pure soft gold, and subsequent development of an alternative, non-cyanide, substrate-catalyzed bath; and (3) development of a new process to electroplate amorphous hard-gold alloys for probable future applications as a contact material on nano-scale electronic devices. (c) 2006 NIMS and Elsevier Ltd. All rights reserved.

Effects of the Cu underlayer thickness and the addition Of Cu to a Sm-Co layer on magnetic properties and microstructure Of SmCo5 thin films exhibiting perpendicular magnetic anisotropy were studied. The origin of the perpendicular magnetic anisotropy was discussed from these experimental results. A thick Cu underlayer of more than 100 nm brought about high perpendicular magnetic anisotropy leading to the squareness ratio equal to unity. The Cu addition enhanced the perpendicular magnetic anisotropy and reduced the Cu underlayer thickness required to obtain the squareness ratio of unity. X-ray diffractometry showed that the crystalline orientation of the Sm-Co layer did not correlate with that of the Cu underlayer. Auger electron spectroscopy revealed that Cu atoms were diffused up to the Sm-Co layer from the Cu underlayer. From the results, Cu atoms existing in the Sm-Co layer were suggested to be strongly related with an appearance of the perpendicular magnetic anisotropy by introducing the Cu underlayer. (c) 2005 Elsevier B.V. All rights reserved.

The covalent attachment of alkyl groups to silicon surfaces, via carbon-silicon bond formation, has been attempted using gas-surface reactions starting from Cl-terminated Si(111) or H:Si(111) under ultraviolet light irradiation. The formation of Cl-terminated Si(111) and its resulting stability were examined prior to deposition of organic molecules. High-resolution electron energy loss spectroscopy (HREELS) was utilized for detecting surface-bound adsorbates. The detection of photo-deposited organic species on CI:Si(111) from gas-phase CH4 or CH2=CH2 was not significant. On H:Si(111), it was evident that after the photoreaction with gas-phase C2H5Cl, C2H5 groups were chemically bonded to the surface Si atoms through single covalent bonds. The C2H5 groups were thermally stable at temperatures below 600 K. Alkyl monolayers prepared on silicon surfaces by dry process will lead to a new prospective technology of nanoscale fabrication and biochemical applications. (c) 2006 Elsevier B.V. All rights reserved.

The effect of the surface morphology of gold-deposited quartz substrate on the enantioselective crystallization of leucine was investigated by using quartz crystal microbalance (QCM) and X-ray diffraction methods. The gold substrate was modified with a self-assembled monolayer with covalently attached D-leucine molecules. For a rough surface with root-mean-square (RMS) roughness of 17 nm, the QCM measurement showed a continuous decrease in frequency, while for a smooth surface with RMS roughness of 2 nm, essentially no change in frequency was observed. Nevertheless, leucine crystals with high crystallinity were clearly formed on the smooth surface.

Magnetic nanoparticles have been attracting much interest as a labeling material in the fields of advanced biological and medical applications such as drug delivery, magnetic resonance imaging, and array-based assaying. In this review, synthesis of iron oxide magnetic nanoparticles via a reverse micelle system and modification of their surface by an organosilane agent are discussed. Furthermore, as a practical biological assay system, the magnetic detection of biomolecular interactions is demonstrated by using the combination of a patterned substrate modified with a self-assembled monolayer and the magnetic nanoparticles.

In conjunction with a study of the copper electrodeposition process from the acid copper sulfate bath for the fabrication of interconnections of printed circuit boards and semiconductor devices, an investigation was performed of the effect of bath additives on the relationship between the ductility of the copper deposit and its crystallographic structure and electrical resistivity. Room-temperature recrystallization, or so-called self-annealing, is known to occur in copper electrodeposits obtained from baths containing Cl-, polyethylene glycol, and bis(3-sulfopropyl)disulfide as additives. Variation with time of the crystallographic orientation, grain size, and resistivity of the deposit was followed over a period of several weeks after the deposition. During the period of self-annealing, ductility was found to increase by a factor of 1.5. The increase in ductility is shown to be related to a change in microstructure of the copper deposit. (c) 2006 The Electrochemical Society.

We studied microscopic magnetic properties of each consistent atom in boron added CoNiFe electroless-deposited soft magnetic films, which is a promising candidate for the soft magnetic underlayer of the perpendicular magnetic recording medium, by X-ray absorption spectra (XAS) and magnetic circular dichroism (MCD) measurement. It was found that various monoxides and Fe sesquioxide coexisted with the metals at the upper part of the films. The results of MCD sum rule showed the expected values of orbital angular moment <L-z> for the film with macroscopic magnetic domain boundaries were larger than those of without domains at Co and Ni atoms and smaller at Fe atom. The appearance of macroscopic magnetic domain boundaries probably originated from the increase in <L-z> of Co and/or Ni atoms. (c) 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

The relationship between human sensation experienced in the use of a material and its physical properties was investigated for the case of writing with a ball-point pen containing water-based ink. Friction force microscopy (FFM) and a writing tester were used to measure friction in nano- and macro-scale, respectively, and their results were correlated with the smoothness of the act of writing. FFM allowed the determination of the optimum concentration of a specific lubricant to be incorporated in the ink to minimize the wear of the bearing material, although no significant relationship was observed with the writing tester. The nano-tribological measurements by FFM provide a significant means to understand the relationship between materials and the smoothness of the act of writing.

This paper describes characteristics of passive direct methanol fuel cell (DMFC), especially the effect of the thickness of electrolyte membrane. Cell performances were compared for membrane electrode assemblies (MEAs) made with Nafion 112, 115, and 117, whose typical thicknesses were 51 &micro;m, 127 &micro;m, and 183 &micro;m, respectively. The MEA made with Nafion 112 showed performance inferior to the other MEAs with thicker membranes. It appears that the mass of methanol permeated to the cathode through Nafion 112 was large, resulting in the loss of a large quantity of fuel, because its thickness was the smallest among the membranes used in this experiment. The observation of fuel level in the reservoir during open circuit stand indicated that most of the fuel was lost by methanol crossover and evaporation due to the rise in cell temperature. Also, the relationship between the concentration of methanol and the electrode potential at open circuit was investigated with a pseudo dynamic hydrogen electrode calibrated against an Ag/AgCl reference electrode. We found that it is essential to overcome the loss of fuel by methanol crossover and evaporation, which decreases the performance of the anode significantly even when the cell is in the stand-by mode.

To enhance the write performance of a CF-SPT head, a smaller main pole of Co-Ni-Fe and a finer coil were fabricated by using the electrodeposition method. Fine coils with 2.5 μm pitch were obtained by the damascene process. The magnetic domain structure of the 15-μm-high and 20-μm-wide main poles could be controlled by changing their taper angles. A head with a favorable domain except at its tip exhibited stable write performance and no pole erasure. Thus, it was concluded that a control of the magnetic domain was necessary for write heads.

The effects of the thicknesses of a Cu/Ti underlayer and a Sm-Co layer on the magnetic properties and domain structure of SmCo₅ perpendicular magnetization films prepared by using an ultra-high-vacuum sputtering system were investigated. By adjusting the thicknesses of both the Cu/Ti underlayer and the Sm-Co layer, the coercivity was controlled to be a moderate value, allowing the films to be used in magnetic recording media while maintaining a squareness ratio of unity. As the Sm-Co layer thickness was reduced, the magnetic cluster size decreased and the magnetization reversal process varied from wall motion mode to a rotation mode. It is suggested that the Cu-rich region in the initial growth stage of the Sm-Co layer functions as the pinning site of the magnetic domain wall and plays an important role in controlling the magnetic domain structure.

Recently embedded passive devices have been actively investigated in an effort to save the surface area on printed circuit boards. About 60% of the area is occupied by the passive parts. As suggested in the previous paper, thin-film capacitors prepared using a semiconductor technology are one of the most promising candidates. In this paper, these film capacitors were embedded using two different methods. One was a conventional method using solder bump, and the other was a newly-developed method using conductive paste. The solder bump was formed using screen-printing following the wafer-level chip-size package (W-CSP) process. Since the solder bump is currently in practical use, high reliability should be expected. However, the chips formed by this method became thicker due to copper posts, solder bumps, and so on. The other method, using conductive paste, has the advantage of connection without any thickness problem. After embedding and solder heat tests, the capacitance of all the chips did not change, and the differences between before and after the tests are within the acceptable margin of error. However, in most cases, the loss (tan &delta;) increased slightly after the embedding and solder heat tests. In only one case did the solder heat test for an embedded BST capacitor chip connected by conductive paste show a lower tan &delta; value than that in the previous test. Based on all the results, the two methods used in this study are concluded to have a high potential for use in embedding methods. Further reliability tests are necessary for practical use.

Mesoporous silica films with uniaxially oriented mesochannels were prepared by dip coating under a steady-homogeneous magnetic field parallel to a substrate. The effect of a strong magnetic field ( 12 Tesla) on the preparation of mesoporous silica films was systematically investigated by using two kinds of templates. When mesoporous silica films with a 2D-hexagonal structure were prepared by using an ionic CTAB ( hexadecyltrimethylammonium bromide)-based precursor solution, the in-plane XRD results of the films proved that the mesochannels were slightly oriented parallel to the magnetic field. When mesoporous silica films were prepared by using a non-ionic P123 ( polyethylene oxide - polypropylene oxide - polyethylene oxide triblock copolymer)- based precursor solution, the directional distribution of the mesochannels became narrow (FWHM was about 20 degrees). The use of large molecules such as triblock copolymers leads to successful magnetically induced orientation. The spatial orientations of the magnetically aligned mesochannels are elucidated by theta - 2 theta XRD, in-plane XRD, cross-sectional transmission electron microscopy (TEM), and high resolution scanning electron microscopy (HR-SEM).

Electroless copper deposition was performed on submicrometer-trench patterned substrates with a bath containing 8-hydroxy-7-iodo-5-quinoline sulfonic acid (HIQSA) as an accelerating additive and polyethylene glycol (PEG) as an inhibiting additive. Void-free copper filling of trenches was achieved by the addition of both HIQSA and PEG at specific concentrations. Copper deposition rate measurements revealed that HIQSA accelerated the deposition only when it was added together with a very low concentration of PEG. The void-free filling is considered to have resulted from the significant acceleration brought about by HIQSA at the trench bottom, where the concentration of PEG is low. (c) 2006 The Electrochemical Society.

Mesoporous intermetallic Pt-Ni alloys with various compositions have been produced by the chemical reduction of two metal (nickel and platinum) salts dissolved in aqueous domains of a lyotropic liquid crystalline (LLC) phase. The mesoporous Pt-Ni alloys are small particles less than 100 nm in size and exhibit high specific surface areas higher than 40 m(2) g(-1). The ordering of the mesostructure decreases with increasing Ni content in the alloys. The high resolution scanning electron microscopic (HR-SEM) images show that the porous nanostructures are indeed formed over the entire area on the external surface of the particles. The lattice parameters of the alloys decrease with the increasing Ni content, implying the incorporation of Ni. The X-ray photoelectron spectroscopic (XPS) data show that Ni atoms in the alloys are thought to be in the zerovalent metallic state (Ni-0). The transmission electron microscopic (TEM) images prove that the lattice fringes assigned to a fcc structure are randomly oriented in the pore walls. The energy-dispersive X-ray spectroscopic (EDS) mapping shows uniform distribution of Ni atoms in the porous matrix. These results indicate the formation of mesoporous intermetallic Pt-Ni alloys.

Two-dimensional hexagonally ordered mesoporous Pt particles are prepared by Pt deposition in the aqueous domains of lyotropic liquid crystals (LLC) by chemical reduction with Zn powders. Interestingly, the framework is composed of connected nanoparticles of about 3 nm in size. Moreover, it is proved that the lattice fringes on the atomic crystallinity are coherently extended across the several nanoparticles in the framework. Such a framework composed of connected nanoparticles with extended crystallinity is uniquely created by using LLC as a soft template, which is not attainable by a traditional approach using mesoporous silica as a hard template. Through the structural identification, the formation mechanism of mesoporous Pt in the presence of LLC is thought to be continuous deposition of Pt nanoparticles from one nanoparticle.

We have proposed a novel convenient pathway via solvent-evaporation-mediated direct physical casting (SEDPC) for the fabrication of mesoporous metals in a micrometer scale. We have presented the successful deposition of highly ordered mesoporous Pt into micrometer channels prepared by lithography. The direct observation by a high-resolution scanning microscope (HR-SEM) showed the formation of highly ordered 2D-hexagonal (p6mm) mesoporous metals onto such substrates. The cyclic voltammogram of the mesoporous Pt in sulfuric acid revealed a typical feature which can identify the clean Pt surface. Moreover, mesoporous Pt exhibits an effective reduction of dissolved dioxygen molecules. It is proved that mesoporous Pt deposited in a very confined area via the SEDPC method possesses electrocatalytic performance owing to Pt. (c) 2005 Elsevier B.V. All rights reserved.

Maskless and electroless fabrication was demonstrated to form patterned nanostructures of various metal species, based upon the process previously developed by the authors. In this process, the metallic nanostructures were formed on the surface of clean, hydrogen terminated p-(1 0 0) Si wafer with pre-patterned nanoscopic defects, which were confirmed to possess higher activity for the reductive deposition reaction of the metal ion species. The deposition was achieved spontaneously and selectively at the defect sites on the wafer surface by immersing into dilute aqueous fluoride solution containing trace amount of metal ion species. By optimizing the formation condition of the patterned defects and composition of the solution, fabrication of patterned nanostructures of various metallic species such as Au, Ag, and Co, was achieved. Formation of the patterned nanostructures to 10 mu m(2) in extent, as well as control of the feature size of the deposits by adjusting the formation condition of the pattemed defects were also attempted. (C) 2005 Elsevier Ltd. All rights reserved.

An investigation was carried out on the surface modification of gamma-Fe2O3 nanoparticles with aminopropylsilyl (APS) groups in 3-aminopropyltriethoxysilane and the interparticle linkage with alpha,omega-dicarboxylic acids (succinic acid and suberic acid) through the terminal amino groups of APS moiety at the surface of gamma-Fe2O3 nanoparticles. It was demonstrated that the change in interparticle distance caused by these surface modifications influences the magnetic property of the composites. When gamma-Fe2O3 nanoparticles were modified with APS groups, coercivity increased and when they were further modified with alpha,omega-dicarboxylic acids, the larger decrease in coercivity was observed with the longer dicarboxylic acid. (C) 2005 Elsevier Ltd. All rights reserved.

A process for electroplating amorphous gold-nickel alloy with the atomic ratio of unity was developed. The plating bath was prepared by adding potassium cyanoaurate(I) into a known plating bath which produces amorphous nickel-tungsten alloy. At a sufficiently high gold concentration, the alloy deposit did not contain any tungsten. The amorphous nature of the Au-Ni alloy produced in the new bath was confirmed by using TEM and THEED. Hardness, resistivity, and contact resistance of this new alloy were determined, and the results are discussed for applications as an electrical contact material. (C) 2005 Elsevier Ltd. All rights reserved.

"All-wet process" for fabrication of Cu wiring on a silicon chip was proposed as a novel ultra-large scale integration (ULSI) interconnect technology for integrated circuits (ICs) applications. Electroless-NiB film was deposited on SiO2/Si substrate modified by self-assembled-monolayer (SAM) activated with PdCl2. The NiB film formed by this method has highly uniform, with good adhesion to the substrate and with good diffusion barrier characteristics against Cu diffusion. Cu was electrodeposited directly on the electroless NiB film that acted as a seed layer. This was done without any conventional conductive or adhesive layer that is conventionally formed by physical vapor deposition (PDV). The thermal stability of electroless NiB layer as a barrier preventing copper from diffusing into the SiO2/Si substrate was evaluated by secondary ion mass spectroscopy (SIMS) and sheet resistance measurement at several annealing temperatures. It was confirmed that the electroless NiB film blocked Cu diffusion and kept the layer integrity under annealing temperatures of up to 400 degrees C for 30 min. The same process of electroless NiB was used for the capping layer that was also formed by "wet process", as the electroless NiB film deposited selectively onto a surface of Cu wiring was also applicable to a capping layer. We conclude that the proposed process is very promising for sub-100 nm technologies as it offers a variety of desirable properties: it has good step coverage while showing good barrier and seed layer properties. (C) 2005 Elsevier Ltd. All rights reserved.

In this study, we investigated the antimicrobial activity of silver nanoparticles (Ag-NPs) and platinum nanoparticles (Pt-NPs) aqueous solution, which were prepared using different stabilizer, such as sodium dodecylsulfate (SDS) and poly-(N-vinyl-2-pyrrolidone) (PVP), for Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) by measuring the minimum inhibitory concentration (MIC). Antimicrobial effect of Ag-NPs for S. aureus and E coli was investigated using cup diffusion method. The growth of Gram-positive (S. aureus) and Gram-negative (E. coli) bacteria were inhibited by Ag-NPs. The MIC of Ag-NPs for S. aureus and E. coli were 5 and 10 ppm, respectively. But the Au-NPs stabilized with SDS did not show antimicrobial activity. Also, the Pt-NPs stabilized with PVP (or SDS) did not show antimicrobial activity for the test organisms. (C) 2005 Elsevier Ltd. All rights reserved.

An investigation was carried out on the effects of the addition of Cu and the thickness of the SmCo5-based thin film with perpendicular magnetic anisotropy upon its magnetic properties, with the aim of reducing the Cu/Ti underlayer thickness. As a result, the Cu/Ti underlayer thickness necessary to obtain the squareness ratio of unity was successfully reduced from 125 to 50 nm. Moreover, for the SmCo5 double-layered perpendicular magnetic recording media with a CoZrNb soft magnetic underlayer, the Cu/Ti underlayer thickness was further reduced to 35 nm. However, the magnetic cluster size and the values of coercivity and saturation field of the SmCo5 media were found to be too large. Thus, we recognized the need for adjusting the cluster size and the magnetic properties to appropriate values, and also the need for investigating the possibility of using this material as patterned media or thermally assisted recording media.

A microscale Bi electrodeposition process was developed and applied to the three-dimensional fabrication of a highly sensitive Xray imaging sensor, so called X-ray microcalorimeter, which has an array of sensing elements with a mushroom-shaped X-ray absorber. The composition and operating conditions for Bi electrodeposition were optimized and flat, smooth Bi deposits were obtained by applying additives such as diethylenetriamine pentaacetic acid (DTPA) and sodium n-dodecyl sulfate (SIDS). The results of ultraviolet (UV)-visible absorption spectroscopy and polarization curves from the Bi electrodeposition solution indicated that the formation of a DTPA-Bi(III) complex and an increase of overpotential for Bi electrodeposition in the presence of SDS improved the solution stability as well as the surface morphology of the deposited film. The mold for the mushroom-shaped microstructure array was formed from a single-layered photoresist coating by applying sequential exposure steps for the "stem" part and the "roof" part. The absorber array was successfully fabricated by the Bi electrodeposition into the mold, precise polishing, and mold removal processes. (c) 2004 Elsevier B.V. All rights reserved.

A CoNiFeB soft magnetic underlayer (SUL) was prepared by electroless deposition using dimethylamineborane as the reducing agent. A 2.5-inch NiP/Al disk was used as the substrate, on which a Nil? nonmagnetic amorphous-layer was also electrolessly deposited. The coercivity H, of as-deposited CoNiFeB films in the direction parallel to the surface exhibited a convex-parabolic dependency on the film thickness. The in-plane M-H loops and the two-dimensional Kerr effect images of the CoNiFeB film showed a nearly isotropic character with H, of 25 Oe and no marked domain boundaries. From magnetic force microscope measurements, we confirmed that these behaviors resulted from the formation of striped magnetic domains caused by slightly perpendicular magnetic anisotropy of SUL. As far as the noise characteristics are concerned, dc noise was increased with H-c, while spike noise was suppressed.

This overview describes our recent study on fabrication processes of high-performance magnetic thin films for high-density magnetic recording. Particularly, it is emphasized that electrochemical processes play significant roles in fabricating the recording heads and media used for the high-density recording. Newly developed electrodeposition methods for fabricating CoNiFe and CoFe soft magnetic thin films with high-saturation magnetic flux density are shown, and the key points for obtaining them are highlighted. It is summarized that the effective seedlayers for the sputter-deposited [Co/Pd],, multilayered films, which are promising candidates as magnetic recording media with strong perpendicular magnetic anisotropy for the high-density magnetic recording, have been developed. We have recently succeeded in developing the novel electroless deposition methods for the CoNiFe-based soft magnetic underlayers of double-layered perpendicular magnetic recording media and for the patterned medium consisting of CoNiP magnetic nano-dot arrays, which are briefly explained. (C) 2005 Elsevier Ltd. All rights reserved.

We have reported in our past work that dectrodeposited Sn-Ni alloy with different composition show considerably different performance as anode materials for Li-ion batteries, and the performance was remarkably well (ca. 650mAh g(-1) at 70th cycle) when the composition was controlled to Sn62Ni38, In this work, structural changes during charge discharge cycling of Sn-Ni alloy with different composition were investigated to evaluate their differences in the cycle performance. From the XRD result, Ni3Sn4 phase was the main phase seen in Sn62Ni38, and its reversible reactivity with Li was confirmed. We suggest that this is the key phase for its high capacity and lengthened cycle life. From Sn54Ni46, which showed low capacity, only a metastable phase close to the structure of SnNi was confirmed. The results from Sn84Ni16 indicated the presence of pure Sn and Sn rich metastable phase would lead to relatively fast electrode degradation. (c) 2005 Elsevier B.V. All rights reserved.

Field effect transistors (FETs) modified with various functional monolayers, such as organosilane monolayer, were formed on the identical substrate by precise control of the fabrication processes. The devices showed a typical transistor property with a good stability in aqueous solutions. The amino monolayer-modified FET acted as an ion sensitive FET with a good pH sensitivity of 58 mV/pH, and the perfluoro-alkyl monolayer-modified FET worked as a reference device. Moreover, the device with enzyme immobilized onto amino modified gate electrode enabled to detect trace concentration (10(-9) to 10(-6) M) of urea with a high sensitivity of 64 mV/decade. These monolayer-modified devices were expected to be applied as working and reference electrodes for on-chip ion and biosensing. (c) 2004 Elsevier B.V. All rights reserved.

To realize highly sensitive electrochemical immunoassays, a micro-fabricated three-dimensional (3D) electrode was fabricated and applied to enzyme immuno assay based on production of a redox species. The dimensions of the electrodes are 10 microm in width and 30 microm in height, with 20 microm spacing in between, and the 30 pairs of anode and cathode electrodes made up a single sensor. This structure lead to enhancement of the electrochemical reaction, nearly 100% of trap ratio of redox species. It can be applied to highly sensitive enzyme immuno sensing based on p-aminophenylphosphate (PAPP). Applicability of this technique to the immuno assay for one of the clinical diagnostic marker proteins (alpha-fetoprotein; AFP) from 6 to 500 ng/mL was demonstrated.

This work studied the design, fabrication, and performance evaluation of a novel micro direct methanol fuel cell (mu-DMFC). A mu-DMFC of 0.018 cm(2) active area was prepared using a series of fabrication steps from micromachined silicon wafer including photolithography, deep reactive ion etching, and electron beam deposition. The novelty of this structure is that we have integrated the anodic and cathodic micro-channels arranged in plane onto a single silicon substrate. This architecture eliminates the need for the membrane electrode assembly (MEA) used in traditional polymer electrolyte-based fuel cells. Another original aspect is the successful electroplating of Pt and Pt-Ru catalysts in the microchannels. In addition, quasi-reference electrodes could be built in the prototype cell. The experimental trials were to verify the feasibility of this novel structure on basis of MEMS technology. The fuel and oxidant were supplied to the unit cell at a rate of 10 mu L/min. Preliminary test results were able to confirm that this new concept of mu-DMFC generates electricity. At ambient temperature under atmospheric pressure, the maximum power density was 0.44 mW/cm(2) at 3 mA/cm(2) with Pt anode catalyst, while the maximum power density reached 0.78 mW/cm(2) at 3.6 mA/cm(2) for cell with Pt-Ru anode catalyst.

In this paper, we discussed the fabrication of micro-channel electrodes for very small DMFC (direct methanol fuel cell), i.e., mu-DMFC, where the channels composed of a current collector and a catalyst layer. The micro-channel electrodes were fabricated on a silicon wafer with a combination of photolithography, chemical etching with potassium hydroxide, spray coating, and electrodeposition method. The catalyst layer formation of Pt and PtRu was achieved by combining pulse electrodeposition with direct current electrodeposition. From these new processes, the mu-DMFC single unit cell was able to be operated for longer time operation compared with that of prototype test cell which was already reported in the previous paper.

Array of macropores filled with electrodeposited Ni was formed on Si substrate applying the novel process, which consists of Si electrochemical etching and Ni electrodeposition using single electrolyte. This electrolyte contained HF as Si dissolution agent and Ni(OSO2NH2)(2) 4H(2)O as Ni2+ source for Ni electrodeposition. First, array of macropores was formed on Si (100) substrate by applying anodic current. The formation was carried out area-selectively by applying Au/Cr micropatterns formed at the back side surface of the substrate as the shade mask, which enables to control the illumination condition for hole generation condition. Subsequently, the applied bias was switched to cathodic current, and Ni was filled into c.a. 200 mu m depth Si macropores without void-like defects. Array of Ni needles with smooth surface was formed area-selectively by removal of the Si region of the Ni filled specimen with 25 wt% tetramethylammonium hydroxide (TMAH) aqueous solution at 90 degrees C.

The heterojunction between Si(111) semiconductor and the well-ordered methyl monolayer was formed to investigate the channel conduction at the surface in the heterojunction structure. With the presence of water, the methyl monolayer/Si heterojunction structure showed switching action with a high trance-conductance of 2.8 x 10(-3) A/V under the application of bias voltage, while without the presence of water, such a switching behavior was not observed. The methyl monolayer/Si heterojunction structure worked as a p-type mode with the presence of water at the modified surface.

A photoassisted anodization process to fabricate arrays of uniform and straight macropores at selected areas of a Si wafer surface was developed. The front- and backside surfaces of n-type Si(100) wafers were coated with a thin Si(3)N(4) layer, and the frontside layer was micro-patterned using photolithography and reactive ion etching to form an array of microscopic openings at selected areas. The inverted pyramid-shape micropits were formed at these openings by anisotropic etching using aqueous KOH solution; these pits act as the initiation sites for the anodization to form macropores. The electrochemical etching was carried out in aqueous HF solution under illumination from the backside of the wafer, on which Au/Cr electric contact was formed following removal of the Si(3)N(4) layer. To improve the uniformity of the formation condition of the macropores at the selected area, holes were area-selectively generated by controlling the illumination condition during the anodization. For this, micropatterns were formed on the Au/Cr layer at the backside surface, which were aligned to those at the frontside surface. The parameters, such as HF concentration, current density, and wafer thickness, i.e., hole diffusion length, were optimized, and the arrays of uniform and high-aspect-ratio macropores were formed at the selected area of the domain at the silicon surface.

A simple microchip device for DNA extraction was constructed based on electrostatic interactions between surface amine groups and DNA. Microchannel was fabricated on silicon wafer by photolithography and coated with 3-aminopropyltriethoxysilane (APTES) or 3-[2-(2-aminoethylamino)-ethylamino]-propyltrimethoxysilane (AEEA) to introduce amine groups on the surface. Determination of the number of surface amine groups and optimization of DNA capture condition were demonstrated to characterize the microchip. Capacities of capturing DNA were approximately 97 ng/cm2 in APTES and 194 ng/cm2 in AEEA modified microchips, respectively. The amount of DNA captured in the microchip increased depending on surface amine density. Furthermore, DNA extraction using amine-coated microchip from whole blood was examined. Quantification of DNA and proteins in washing or eluting fraction indicates that proteins were removed at washing steps and only DNA was effectively eluted by changing alkalinity of buffer from pH 7.5 to 10.6. The amount of DNA extracted from whole blood was approximately 10 ng and its recovery ratio was 27-40%. Performance of PCR for the eluted fraction indicates that DNA extracted from whole blood was well purified using amine-coated microchip.

Effects of the Pd seeds formed by an electrochemical process on the microstructures of Co/Pd multilayered perpendicular recording media were investigated. By immersing a CoZrNb soft magnetic underlayer (SUL) into PdCl2 aqueous solution, island-like Pd clusters were deposited on the SUL, resulting from the electrochemical substitution reaction. Transmission electron microscopic observations revealed that the columnar Co/Pd multilayered grains with clear boundaries grew on the SUL with the Pd clusters. The clear grain boundaries, where the densities of Co and Pd elements were low, were thought to cause the magnetic exchange decoupling between the Co/Pd grains, leading to an increase of perpendicular coercivity and a decrease of magnetic cluster size of Co/Pd multilayered film. Consequently, lower medium noise was obtained for the Co/Pd multilayered medium with the Pd clusters than for that with a sputter-deposited Pd seedlayer. From these investigations, it was clarified that the SUL surface with Pd clusters provided the effective nucleation sites for a well-defined Co/Pd multilayered grain growth. (C) 2004 Elsevier B.V. All rights reserved.

SmCo5 thin films with Cu seedlayer exhibiting perpendicular magnetic anisotropy were studied. The perpendicular magnetic anisotropy was enhanced using the Sm-Co layer formed by laminating Co and Sm sub-layers alternately. The Co/Sm laminate structure promoted the crystallization Of SmCo5 and the preferred orientation of its c-axis. The perpendicular magnetic anisotropy was further improved by suppressing the surface roughness of the Cu seedlayer. The SmCo5 thin film prepared in this study possesses an adequate corrosion resistance when judged by an electrochemical analysis. (C) 2004 Elsevier B.V. All rights reserved.

Electroless deposition process for fabricating magnetic dot arrays was studied. A patterned Si substrate with a SiO2 resist was produced by processes combined with electron-beam lithography and reactive ion etching. By immersing the patterned Si substrate into a CoNiP electroless deposition bath, CoNiP was deposited only into the patterned pores, demonstrating a satisfactory area selectivity of the deposition. Excellent uniformity on the CoNiP deposition into the patterned pores with diameter less than 100 nm and high aspect ratio (&gt; 5) was achieved by applying chemical activation processes using a Pd solution prior to the deposition. The CoNiP dot arrays exhibited higher perpendicular squareness ratio than that of CoNiP continuous film and showed a clear magnetization state at DC-magnetized state, which originated from the shape anisotropy caused by high aspect ratio of the dot patterns. (C) 2004 Elsevier B.V. All rights reserved.

A novel fabrication process of a soft magnetic underlayer (SUL) for a double-layered perpendicular magnetic recording medium was presented. The CoNiFeB SUL was deposited on a silicon disk substrate using an electroless deposition. The Ni seed layer for the electroless deposition was prepared by an electrochemical process. The surface of the deposited SUL was subjected to a chemical mechanical polishing to be flattened, and R-a value of the SUL was less than 0.4 nm. A magnetic domain structure greatly depended on the electroless deposition condition. Particularly, the control of an agitation speed during electroless deposition is much effective for the suppression of distinct domain walls appearing in CoNiFeB underlayers. (C) 2004 Published by Elsevier B.V.

Effects of N-2 additive gas and/or substrate heating during the sputtering of [CoB/Pd](20) multilayered films on the magnetic properties and microstructure were investigated. The [CoB/Pd](20) film fabricated at 20degreesC by adding N-2 gas during sputtering possessed the finest grain size and the smallest magnetic cluster size among media fabricated in this study although the film sputter-deposited at 260 degreesC by adding N-2 gas exhibited the weakest intergranular exchange coupling. It was revealed that the double-layered perpendicular magnetic recording medium that consisted of the [CoB/Pd](20) film fabricated at 20degreesC by adding N-2 gas exhibited the highest signal-to-noise ratio in the read write characteristics. (C) 2004 Elsevier B.V. All rights reserved.

Nanosized electrodeposited 62 atom % Sn-Ni alloy was tested to highlight the effects of volume changes on the cycling life of the electrode during lithiation and delithiation. X-ray diffraction showed that the Ni3Sn4 was the main phase of the as-deposited alloy. A unique feature of the 62 atom % Sn-Ni is that it exhibited a capacity recovery upon cycling. When cycled galvanostatically, the Sn62Ni38 offers low capacity fade while reversibly incorporating lithium up to 600 mAh/g. At the first charge LiSn alloy phases are formed. This led to volume expansion of the electrode causing the formation of cracks. At the following cycles the Ni3Sn4 phase was restored and preserved over extensive cycling revealing the reversibility of the reaction between Ni3Sn4 and Li+. As to the reasons of the capacity recovery noticed with this alloy, scanning electron microscopy images provided evidence of modifications of the surface condition accompanying a volume change during cycling. The chemical diffusion coefficient (D-Li) value determined from electrochemical impedence spectroscopy measurements during lithium insertion was within 10(-9) to 10(-10) 10 cm(2) S-1. (c) 2005 The Electrochemical Society. [DOI: 10.1149/1.1856913] All rights reserved.

The spontaneous deposition of Ni on Si(100) surface in aqueous alkaline solution was investigated under various conditions. In a 0.1 M NiSO4 solution containing 0.2-0.5 M (NH4)(2)SO4, the optimum pH for the homogeneous deposition at 60-80degreesC at each set of operating conditions shifted in the high-pH direction as both (NH4)2SO(4) concentration and the operating temperature were decreased. The potential at which the deposition terminates and the deposition duration were determined from electrochemical open-circuit potential profiles. The different behaviors, observed at different pH levels, are discussed in terms of these potential measurements. Ultraviolet-visible absorption spectra of various Ni solutions used indicated that the deposition behavior was strongly affected by the composition of the Ni complex and the reactivity of Si surface. The deposition reaction efficiently proceeded when the Ni complex was present in a specific composition. The anodic reaction rate of Si decreased steeply when the solution temperature was lowered. The optimum condition for the homogeneous deposition was greatly affected by the reactivity of the Si surface rather than the composition of the complex, the higher pH favoring the overall reaction. (C) 2004 The Electrochemical Society. All rights reserved.

Effects of the conventional bath additives [chloride ions (Cl-), poly(ethylene glycol) (PEG), bis(3-sulfopropyl)disulfide(SPS), and Janus green B (JGB)] used in the damascene process on the filling of submicrometer trenches with electrodeposited copper were investigated by electrochemical polarization measurement and cross-sectional microscopy. The combination of Cl- and PEG inhibited copper deposition in the areas of opening of the trenches, while SPS accelerated it at the bottom. Polarization curves showed that the degree of acceleration of copper deposition by SPS increases with the concentration of SPS. This SPS concentration- dependent acceleration accounts for the observed bottom- up growth. The addition of JGB inhibited copper deposition at the later stages of the filling process, leading to the suppression of the overfill phenomenon, although the bottom-up growth was also inhibited at high JGB concentrations. Bath agitation significantly enhanced the inhibition effect of JGB on the overfill phenomenon, without disturbing the bottom-up growth. (c) 2005 The Electrochemical Society. All rights reserved.

This article summarizes our recent studies on the synthesis of highly ordered mesostructured Ni and Ni-Co alloys by electroless deposition method. We propose that a careful control over the nucleation as well as the grain growth by reducing agents can lead to the fort-nation of a highly ordered mesostructure from a lyotropic liquid crystalline phase (LLC). The sophisticated combination of dimethylamineborane (DMAB) and sodium borohydride (SBH) in an electroless plating bath produces highly ordered mesoporous Ni, and this technique can be extended to prepare a series of mesostructured Ni-Co alloys with various compositions. The composition of the alloys can be varied easily by controlling the metal compositions in the plating bath.

Mesostructured Ni and Co particles are formed by metal deposition in the aqueous domains of lyotropic liquid crystals (LLC) using different reducing agents. We have investigated the role of reducing agents in metal deposition for the synthesis of highly-ordered mesoporous metals by electroless deposition. Slow metal deposition accompanied by the autocatalytic reaction of dimethylamineborane ( DMAB), caused by the combination of Ni and DMAB, led to the formation of highly-ordered mesostructured Ni.

Nickel particles with a highly ordered mesostructure are prepared by electroless deposition of Ni salts dissolved in aqueous domains of lyotropic liquid crystalline (LLC) media made of a nonionic surfactant (Brij 56) at a high concentration. The mesostructure inside the Ni particles after the electroless deposition has a macroscopic alignment of mesochannels derived from the LLC media which are composed of crystalline domains on a micrometer scale. It is proved that the arrangements of rod-like self-assemblies in the LLC indeed work as a scaffold to direct the grain growth of Ni. This is the first direct evidence of direct physical casting from LLC. (c) 2005 The Electrochemical Society.

Recently, there has been a strong demand for smaller electronic devices with improved. About 60% of the area is occupied by the passive components for packaging. To overcome this limitation, an embedded capacitor was prepared using semiconductor technologies and the process technology of ferroelectric random access memories. Eight micro capacitors were prepared in a 2 mm² area. Two types of high dielectric constant material were used. The first one is Barium Strontium Titanium oxide (BST) for focusing high capacitance with high loss, and the other is Strontium Bismath Tantalum oxide (SBT) for focusing low loss with medium capacitance. The micro capacitor with BST, whose dielectric constant (&epsilon;) was 350, showed about 3200pF at 0 bias and its loss, tan &delta;, was a little lower than 0.01. The one with SBT, whose &epsilon; was 51, showed 470 pF, and its tan &delta; was about 0.001. It is concluded that micro capacitors with the requested characteristics were prepared.

By a contact plating technique using a galvanic reaction between Al and An in the presence of Pt complex, we have for the first time succeeded in the formation of a highly ordered meso-structured Pt film on a An surface by reduction of Pt ions in the presence of lyotropic liquid crystals.

Thin films of SmCo5 with extraordinarily high perpendicular magnetic anisotropy were prepared by introducing a Cu/Ti dual underlayer and controlling the substrate temperature during the sputter deposition. Under optimized conditions, the magnetic anisotropy constant reached 4.0x10(7) erg/cm(3), and the coercivity and the remanence ratio in the direction perpendicular to the film surface were 12.0 kOe and unity, respectively. The high perpendicular magnetic anisotropy is attributed to the high degree of preferred orientation of the c axis; the full width at half maximum in the rocking curve of SmCo5(002) reflection was 3.1degrees. (C) 2004 American Institute of Physics.

For developing a magnetic bioassay system, an investigation to determine the presence of a specific biomolecular interaction between biotin and streptavidin was done using magnetic nanoparticles and a silicon substrate with a self-assembled monolayer. Streptavidin was immobilized on the magnetic particles, and biotin was attached to the monolayer-modified substrate. The reaction of streptavidin-modified magnetic particles on the biotin-modified substrate was clearly observed under an optical microscope. The magnetic signals from the particles were detected using a magnetic force microscope. The results of this study demonstrate that the combination of a monolayer-modified substrate with biomolecule-modified magnetic particles is useful for detecting biomolecular interactions in medical and diagnostic analyses.

This work studied the design, fabrication, and performance evaluation of a 36 cm(2), passive, air-breathing, room-temperature, direct methanol fuel cell (DMFC). The cell is completely passive with no external pumps or other ancillary devices. It takes oxygen from the surrounding air, and the methanol solution is stored in a built-in reservoir. The fuel cell runs successfully with methanol concentration ranging from 0.5 to 4 M. It produced a power density of 11 mW cm(-2) reached with 4 M methanol at current densities as high as 36 mA cm(-2) and at a voltage of 0.3. (C) 2004 Elsevier B.V. All rights reserved.

In this work, we describe the fabrication of a room temperature operating direct methanol fuel cell (DMFC) device for portable electronic devices and its performance as an electrical power source for portable phone. The cell stack is completely passive without external pumps or other ancillary devices. It takes oxygen from the surrounding air, whereas the methanol solution is stored in a built-in reservoir. We achieved a maximum power as high as 2 W, which is largely commensurate with cell phone requirements. The DMFC coupled to DC-to-DC converter was capable of powering a cell phone. The maximum power consumption for talk mode was of 1.2 W while 1.8 W was withdrawn from the stack when receiving a call.

An X-ray microcalorimeter is a high performance X-ray spectrometer that can achieve both high energy resolution of conventional wavelength dispersive spectrometers (WDS) and high quantum efficiency of energy dispersive spectrometers (EDS). The energy resolution can be theoretically improved to about 1 eV, which value is 120 times better than that of conventional Si(Li) spectrometers and nearly 100% of quantum efficiency can be achieved using microabsorbers. In order to realize high energy-resolution X-ray imaging using an array of X-ray microcalorimeters, two types of 2 x 2 X-ray microcalorimeter arrays were fabricated and tested. Using an X-ray microabsorber so-called "mushroom-shaped" X-ray microabsorber, the filling factor was enhanced to about 70%. We tested Sn and Bi as an X-ray microabsorber. Consequently, the Sn absorber degrades the energy resolution because of the long time constant. This problem was cleared using the Bi microabsorber. The achievable energy resolution was also investigated. As a result, the energy resolution of 6.3 eV was obtained with the test device. (C) 2004 Elsevier B.V. All rights reserved.

Co-Fe soft magnetic thin films with high-saturation magnetic flux density B-s were prepared by electrodeposition. The B-s value of the Co-Fe alloy films deposited from the conventional cell system is lower than that of bulk alloys. With the use of a separated compartment dual cell system, the B-s value of the Co-Fe alloy films was reached the same as that of bulk alloy. The coercivity H-c values were higher than 12 Oe; however, the H-c value could be lowered to 8 Oe by annealing in vacuum with an applied magnetic field. It is suggested that decreasing H-c of the films by annealing is caused by relaxation of lattice distortion. In addition, the high-B-s Co-Fe films show good corrosion resistance.

We present a novel fabrication process for a soft magnetic underlayer of a CoNiFe-based alloy for a double-layered perpendicular magnetic recording medium using electroless deposition. The electroless-deposited CoNiFeP film is focused on as the soft magnetic underlayer. The CoNiFeP soft magnetic underlayer was fabricated on a 2.5-in glass disk with a Ni/Ti seed layer and the substrate was rotated in an electroless deposition bath under a magnetic field applied. The CoNiFeP underlayer as deposited was flattened using a chemical mechanical polishing, and the film thickness thereby became about 1 mum. The in-plane coercivity and saturation magnetic flux density of the CoNiFeP underlayer were less than 2 Oe and more than 12 kG, respectively. The magnetic domain observation revealed that the CoNiFeP underlayer electroless deposited under the magnetic field applied and the substrate rotated exhibited no marked domain boundary, vanishing a spike noise in read-write experiments. A double-layered perpendicular magnetic recording medium with the electroless-deposited CoNiFeP film showed a sufficient overwrite performance and high signal-to-noise ratio as compared with a typical soft magnetic underlayer fabricated using sputtering.

Pd cluster seeds for a double-layered perpendicular magnetic recording medium composed of a Co/Pd multilayered film and a CoZrNb soft magnetic underlayer (SUL) were fabricated with an electrochemical treatment. By immersing the SUL into an aqueous PdCl2 solution, the substitution of Pd for Co at the surface of the SUL took place, which was caused by the difference in electrochemical redox potential between Pd and Co. Uniformly distributed Pd clusters with 8 nm in diameter were successfully formed with the treatment for the optimized duration. Use of the Pd clusters as the seeds for deposition of the Co/Pd multilayered film increased the perpendicular coercivity and reduced the size of magnetic cluster of the film. These results suggested that the Pd cluster seeds led to the formation of magnetically isolated Co/Pd multilayered grains, improving the magnetic properties of Co/Pd multilayered film.

A 10 nm Pd/Si dual thin film was developed as a seed layer for a Co/Pd multilayer in double-layered perpendicular magnetic recording media. The Pd/Si seed layer, sputter deposited under Ar sputtering gas containing N-2 and postannealed at 400 degreesC, markedly reduced intergranular exchange coupling of the Co/Pd multilayered film, resulting in a decrease in both the slope parameter, defined as 4pi(dM/dH)(H=Hc), and the magnetic cluster size. Consequently, medium noise was essentially reduced, thereby improving the signal-to-noise ratio of the Co/Pd recording media on a CoZrNb soft magnetic underlayer. The addition of N-2 gas effectively decreased the grain size of Pd in the seed layer. A Pd/Si seed layer prepared with both processes exhibited a granular structure of fine Pd-rich grains surrounded by a Si-rich amorphous region, which provided nucleation sites for the growth of well-separated Co/Pd multilayered grains. (C) 2004 American Institute of Physics.

Microscale Bi electrodeposition process was developed to fabricate the array of mushroom-shaped absorbers for the high sensitive X-ray imaging sensor, so called X-ray microcalorimeter array. The bath composition and operating conditions for Bi electrodeposition was optimized, and sufficient bath stability and surface smoothness of the deposits were achieved by applying the additives such as diethylenetriamine pentaacetic acid and sodium n-dodecyl sulfate with appropriate concentration. By applying the two-step exposure steps for the "stem" part and the "roof" part, the mold to deposit the mushroom-shaped microstructure was formed from single-layered photoresist coating. The absorber array was successfully fabricated by the sequential processes of Bi electrodeposition into the mold, precise polishing, and mold removal.

The oxidation mechanism of TiCl3 as a reductant for an electroless deposition process was studied by ab initio molecular orbital method. The reaction process of TiCl3 proceeds with the substitution of Cl- to OH-. Net charge and spin density of the reactant, product, and intermediates were evaluated. It was suggested that the electron emission of TiCl3, which is originated by the oxidation of Ti(III) to Ti(IV), took place when Cl is replaced by OH- to form Ti(OH)(4). The catalytic activity of the metal surface, which is one of the most important factors for the electroless deposition process, was studied using a Pd-4 Cluster as a model surface. It was suggested that the Pd-4 cluster enhanced the reaction of TiCl3 to emit the electron. The effect of solvation is also taken into account in terms of the dielectric field constant. It was indicated that the heat of oxidation reaction shifted to an exothermic reaction with decreasing dielectric constant, indicating that the reaction preferentially proceeds in the vicinity of solid/liquid interface. However, it was indicated that the reaction could proceed in the bulk solution, suggesting that appropriate stabilization such as formation of complex is required for the application of the TiCl3 to the electroless deposition process.

A design for a novel micro direct methanol fuel cell (mu-DMFC) of 0.018 cm(2) active area is described. The mu-DMFC was prepared using a series of fabrication steps from micro-machined silicon wafer including photolithography, deep reactive ion etching, and electron beam deposition. The novelty of this structure is that we have fabricated the anodic and cathodic micro-channels arranged in plane, dissimilar to the conventional bipolar structure. The first objective of the experimental trials was to verify the feasibility of this novel structure on basis of MEMS technology. Preliminary testing results show that this new concept L-DMFC generates electricity. (C) 2004 Elsevier B.V. All rights reserved.

Highly ordered mesoporous Ni particles have been prepared by electroless deposition using lyotropic liquid crystals as templates. The bath conditions, in particular the kind of the reducing agents, greatly affected the degree of the ordering of mesostructures. By using well chosen appropriate reducing agents and combining those agents, we have succeeded in synthesizing Ni particles with highly ordered mesoporosity.

We report the synthesis of SnSb-based intermetallic with improved morphology. The electrochemical characterization shows that these materials have a good electrode behavior in a lithium cell. Capacities exceeding 800 mAh/g with a charge-discharge efficiency approaching 100%, have been obtained. In addition, the percent of the initial irreversible capacity is moderate. The capacity decreases upon cycling quite likely due to a still not optimized electrode structure. (C) 2004 Elsevier B.V. All rights reserved.

The corrosion behaviour of a CoNiFe film prepared by electrochemical processes has been investigated. Corrosion resistance is very important for materials to be used in electrical devices for practical use. For example, soft magnetic materials are used as the core materials of magnetic recording heads. In particular, electrodeposited CoNiFe thin films with a high saturation magnetic flux denisity are suitable for this application. The corrosion resistance of the CoNiFe film is strongly influenced by its composition, crystalline structure, and presence of impurities. A fine crystalline structure containing no impurities is one of the most important characteristics of CoNiFe soft magnetic thin films with high corrosion resistance.

An X-ray microcalorimeter is a cryogenic energy-dispersive spectrometer, which has an energy resolution almost comparable to that of conventional wavelength-dispersive spectrometers. Using a transition edge sensor (TES) as a temperature sensor, the energy resolution can be further improved. We have developed a new method of achieving an array of TES microcalorimeters for the purpose of X-ray imaging. To achieve this, mushroom-shaped X-ray microabsorbers formed using electrodeposition were applied. The temperature of the TES, which is easily degraded by thermal diffusion, was kept sufficiently low throughout the process to achieve practical use. On the bases of this new method, a 2 x 2 (x 4) array of TES microcalorimeters was fabricated and tested. A high energy resolution of 13.0 eV at 6 keV was achieved and the filling factor was improved to 83%. Although several issues still need to be investigated, we verified that our method is useful for fabricating a Ti-Au TES microcalorimeter array.

We are developing a Ti/Au TES microcalorimeter array for future Japanese X-ray astronomy missions. The goal is an energy resolution of 2-5 eV at 6 keV, and an array of 100-1000 pixels to achieve a geometrical area of &gt;1 cm(2) and a moderate spatial resolution simultaneously. The energy resolution was improved to similar to6 eV at 6 keV with a very fast time constant (&lt;100 mus). To achieve a high coverage fraction, it is necessary to fabricate mushroom-shaped X-ray microabsorbers. We are developing an electrodeposition fabrication technique that is suitable for our process. Sn was used as absorber material, but the energy resolution was not good due to the existence of long-lived quasiparticles. Bi is also used, and the process is under optimization now. The readout strategy is to multiplex signals in the frequency domain, using a bridge circuit. So far, we succeeded in multiplexing two pixels modulated with 50 and 20 kHz at 440 mK. The energy resolution obtained at 110 mK was 33 eV (25 kHz). (C) 2003 Elsevier B.V. All rights reserved.

Performance of microcalorimeters with a Ti/Au transition-edge sensor (TES) and an electrodeposited absorber has been investigated. The absorbers are in a mushroom-shape made of Sn or Bi. With an Sn absorber we observed a long time scale component of 1.8 ms for X-ray pulses, which is due presumably to recombination of quasiparticles into phonons. As a result, the energy resolution is not good with the Sn absorber. Better energy resolution of 28 +/- 1 eV was obtained with an incomplete-shaped Bi absorber, although the long component was also seen with smaller level. A calorimeter with only a neck of the An seed layer for the electrodeposition had the best energy resolution of 6.3 +/- 0.4 eV in spite of saturated pulses and relatively high transition temperature of 210 mK. (C) 2003 Elsevier B.V. All rights reserved.

We have developed multi-pixel TES microcalorimeters in order to realize high-energy resolution and X-ray imaging. A Sn absorber and a Bi absorber were formed on Si3N4 and SiO2 membrane using two-step exposure photolithography and electrodeposition. A FEM analysis was carried out to investigate the performance of the X-ray microabsorbers. In addition, a superconducting through-wafer interconnection was demonstrated considering the future X-ray imager using microcalorimeters. Detail of the fabrication techniques, characteristics and simulation results of two types of the microabsorbers, as well as those of the calorimeters are described. (C) 2003 Elsevier B.V. All rights reserved.

Enantioselective crystal growth of leucine occurs on a solid surface modified with a self-assembled monolayer depending on the chirality of the enantiomer attached, as evidenced by the X-ray diffraction method.

In this work, the co-continuous polymer blend was synthesized for use as the electrolyte in lithium batteries. Such electrolytes were characterized by a co-continuous morphology consisting of two three-dimensionally interpenetrated polymer networks simply formed by hot-mixing two nonmiscible polymers. A preliminary electrochemical characterization of the gelified co-continuous polymer blend as electrolyte for lithium batteries is also reported. (C) 2004 The Electrochemical Society.

Mesostructured binary Ni - Co alloys with various compositions are prepared for the first time by the electroless deposition of metal salts ( nickel and cobalt) dissolved in aqueous domains of the lyotropic liquid crystalline phases of a non-ionic surfactant ( Brij 56) at high concentrations. Mesostructured alloys with various Ni/Co ratios are easily obtained by changing the composition of the baths, leading to the control of saturation magnetization. The composition of the alloys affects the ordering of the mesostructure; higher Co content lowers the ordering.

Chiral discrimination between thalidomide enantiomers was achieved using the self-assembled monolayer (SAM) of an atropisomeric compound, 1,1'-binaphthalene-2,2'-dithiol (BNSH), which takes a two-dimensional chiral arrangement on gold(111) surface. Interestingly, an "all-or-none" type enantioselectivity appears; one enantiomeric form of BNSH SAM allows the adsorption of only one enantiomer of thalidomide. In addition, the response of a racemic SAM of BNSH was revealed to be one-half of that caused by pure enantiomeric SAM.

We are developing a superconducting transition-edge sensor (TES) microcalorimeter array for the Diffuse Intergalactic Oxygen Surveyor (DIOS) mission. DIOS is a relatively small Japanese X-ray mission which will study large-scale distribution of the warm-hot intergalactic medium (WHIM) using O-VII and O-VIII emission lines. The satellite weighs about 400 kg equipped with a four-reflection X-ray telescope (FXT) and a TES microcalorimeter array (XSA). The design goal of the observing system is an effective area larger than 100 cm 2 at the oxygen line energy, a field of view about 50 arcmin square, and an energy resolution about 2 eV in the energy range of 0.3-1 keV. The TES microcalorimeter array provides the large field of view and good energy resolution at the same time. We plan to install an array comprising 16 x 16 pixels with an overall size of 1 cm square, which is cooled with a cryogen-free cooler. Pixels are readout by multiplexing signals using a multi-input SQUID amplifier, with each input connected to a TES microcalorimeter which is AC biased with a different frequency. We report the design and present status of the XSA system development.

According to HAUP measurements, two ferroelectric boracites, Fe3B7O13I and Cu3B7O13CI, manifest peaks of a gyration component g(11) at each Curie point. These phenomena are entirely unintelligible from the usual concepts of the origin of ferroelectricity. Besides, the electrogyration effects of both crystals are also quite different. As has already been determined boracite crystals exhibit characteristic features of being improper ferroelectric. A phenomenological theory of improper ferroelectricity developed by Kobayashi is applied to these anomalous phenomena, and qualitative interpretations are successfully obtained.

This overview describes the results of our recent study of the application of electrochemical nanotechnology to the fabrication of magnetic recording materials, interconnects in ultra-large-scale integrated (ULSI) devices, energy storage materials, and on-chip biosensors. It is important to note that electrochemical processes play significant roles in developing and fabrication such sophisticated materials and devices. In the field of magnetic recording, electrodeposition methods for preparing CoNiFe and CoFe soft magnetic thin films with a high saturation magnetic flux density were newly developed, and the significant issues for obtaining those films are highlighted. In the area of ULSI interconnects, we developed a technique using a self-assembled monolayer (SAM) for direct bonding of the interconnect layer to SiO2, and proposed a novel electroless deposition method for fabricating a diffusion barrier layer. In the field of batteries, electrodeposited SnNi alloy was proposed as a future anode material for Li batteries, and electrochemical MEMS processes were shown to be useful for fabricating micro-sized direct methanol fuel cells (DMFCs) as portable batteries for electronics applications. In the area of chemical sensors, we developed a new process for fabricating field effect transistors (FETs) modified with SAMs for on-chip biosensing applications.

Nanometer-size particles of iron oxide were prepared by a successive reduction-oxidation of ferric or ferrous ions within reverse micelles. Nanoparticles of iron oxide were collected from reverse micellar solution as precipitates by adding modifier molecules. The X-ray diffraction patterns and magnetic properties of thus-prepared samples suggested the formation of nanocrystalline phase of maghemite, gamma-Fe2O3.

We propose a polymer blending method for preparing the PEO (polyethylene oxide)-LiBF4 complex electrolyte for lithium secondary battery applying to the IPN (interpenetrated polymer network) gel electrolyte. The polymer blend mixture of PEO-PS (polystyrene) -LiBF4 was prepared as a film by the hot-pressing method. The resulting IPN film was plasticized with the electrolyte solution of 0.5 M LiBF4/EC (ethylene carbonate) -PC (propylene carbonate) (I : I vol.), in which the formation of PEO-LiBF4 complex was confirmed by the Raman spectroscopy. The basic properties as an electrolyte of Li metal batteries, i.e., ionic conductivity, chemical stability at the polymer gel electrolyte/lithium metal interface, and charge-discharge performance of the Li/(PEO-LiBF4/PS) gel electrolyte/LiCoO2 cell were studied and discussed.

It was found that the addition of propargy alcohol (PA) to a nickel sulfamate solution was effective for controlling the shape of deposit in the process of nickel electrodeposition onto a micropatterned substrate. The factors, i.e. the electrode potential, the thickness of diffusion layer and the concentration of PA, that affect the shape control function of PA were simulated by the boundary element method, based on the assumption that PA is consumed by diffusion-adsorption-reduction mechanism and that the concentration of PA vary along the cathode/solution interface. The function that represents the variation of PA concentration along the interface was used for the boundary values. The results of simulation explained well the difference in growing habit of the deposits obtained experimentally at different potentials, and figured out the important factors for suppressing the growth in horizontal direction. The optimum conditions for obtaining probe shape deposits were proposed.

Sn electrodeposition was employed for fabricating an array of microabsorbers with a 'mushroom-shaped' microstructure for a precision X-ray microdetector, the so called X-ray microcalorimeter. A deposition process for flat and smooth Sn films, which was suitable for the use of the absorber material, was developed by optimizing the conditions of additives such as o-cresol-4-sulfonic acid and polyethyleneglycol (PEG) to the Sn bath. The Sn films exhibited suitable properties, i.e. a higher superconducting transition temperature than the operating temperature of the X-ray microcalorimeter. The mushroom-shaped absorber array was successfully fabricated by Sn electrodeposition in combination with a photolithographic technique. (C) 2002 Elsevier Science B.V. All rights reserved.

As is well known, contamination of the silicon surface by trace metal impurities is responsible for detrimental effects in the production of ULSI circuits. An extensive experimental study of the factors influencing the spontaneous metal nucleation from fluoride solutions on Si substrates was undertaken. In acidic media (dilute HF solution) only noble metals can be deposited. The mechanism for the formation of Cu element nuclei was chosen as a model example. The first stage was the appearance of Cu crystals of a nanoscopic scale, observed by AFM microscopy. These nuclei soon induce corrosion pits due to the formation of a short-circuited electrochemical cell. In concentrated NH4F solutions, the open circuit potential (ocp) of Si samples is highly negative and provides an efficient driving force for nucleation even for common metals like Fe. Our results show that the deposition of Fe is hardly observable when Fe only is present, but in the presence of Cu, a catalytic effect is observed leading to the co-deposition of Fe + Cu nuclei. In all cases surface defects on the Si substrate are generated by the corrosion pits. (C) 2002 Elsevier Science B.V. All rights reserved.