KINDAI UNIVERSITY


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湯浅 雅賀ユアサ マサヨシ

プロフィール

所属部署名産業理工学部 生物環境化学科 / 産業理工学・産業技術研究科
職名講師
学位博士(工学)
専門無機材料化学
ジャンル科学・技術/化学
コメンテータガイドhttp://www.kindai.ac.jp/meikan/1369-yuasa-masayoshi.html
ホームページURLhttps://kaken.nii.ac.jp/d/r/50404075.ja.html
メールアドレス
Last Updated :2017/11/21

コミュニケーション情報 byコメンテータガイド

コメント

    エネルギー技術や環境技術に貢献するための機能性無機材料について研究しています。特に、次世代の大容量蓄電池として注目されている金属空気電池や環境計測用ガスセンサを開発しています。

学歴・経歴

学歴

  • 2003年04月 - 2005年05月, 九州大学, 大学院総合理工学府, 物質理工学専攻
  • 2001年04月 - 2003年03月, 九州大学, 大学院総合理工学府, 物質理工学専攻
  • 1998年04月 - 2001年03月, 九州大学, 工学部, エネルギー科学科

経歴

  •   2016年10月,  - 現在, 九州工業大学(非常勤講師)
  •   2015年04月,  - 現在, 近畿大学(講師)
  •   2007年04月,  - 2015年03月, 九州大学(助教)
  •   2005年06月,  - 2007年03月, 九州大学(助手)

研究活動情報

研究分野

  • 総合工学, エネルギー学
  • 材料化学, 機能材料・デバイス
  • 複合化学, 機能物質化学

研究キーワード

  • 工業無機化学, ナノ材料, 電池, ナノ粒子合成, 無機工業化学, 空気電池, 放電特性, ナノ粒子, ガスセンサ, 半導体, 薄膜, 環境ガス, 分子認識, クラスター粒子, 電気化学, ガス拡散, ゾル, マイクロ素子, 設計, 高次構造, 酸化スズ, 担持, メソマクロポア制御, マスキング, VOC, センサ, 酸化タングステン, メソマクロポア

書籍等出版物

  • 電気化学/インピーダンス 測定のノウハウと正しい データ解釈, 湯浅雅賀 他47名, 共著, 第3章第3節 pp.362-365「ガス拡散型電極の電位測定法」, 技術情報協会,   2013年05月
  • 触媒調製ハンドブック, 湯浅雅賀 他224名, 共著, 第2編3章09節 pp.188-189 「ペロブスカイト型 酸化物の合成(逆ミセル法)」, エヌ・ティー・エス,   2011年04月

MISC

  • Visible-light sensitization and photoenergy storage in quantum dot/polyoxometalate systems, Tetsuya Kida, Hiromasa Furuso, Kota Kumamoto, Azzah Dyah Pramata, Masayoshi Yuasa, Kengo Shimanoe, Chemistry - A European Journal, 21, 7462, 7469,   2015年05月11日, 10.1002/chem.201500021, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84928721669&origin=inward
    概要:© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Abstract Recently, the process by which energy is transferred from photoexcited semiconductor nanocrystals, called quantum dots (QDs), to other semiconductors has attracted much attention and has potential application in solar energy conversion (i.e., QD-sensitized solar cells). Sensitization of wide band gap polyoxometalates (POMs) to visible light by using CuInS2 QDs dispersed in an organic solution is demonstrated herein. Photoluminescence quenching and lifetime studies revealed efficient electron transfer from the CuInS2 QDs to POMs, such as SiW12O40 and W10O32, that were hybridized with a cationic surfactant. CuInS2 QDs function as an antenna that absorbs visible light and supplies electrons to the POMs to enable certain photocatalytic reactions, including noble-metal-ion reduction. The photoenergy storage capabilities of the QD-POM system, in which electrons photogenerated in QDs by visible-light excitation are trapped and accommodated by POMs to form reduced POM, are also demonstrated. Electrons stored in the POM can be later discharged through reductive reactions, such as oxygen reduction, in the dark. Enhanced capabilities: CuInS2 quantum dots (QDs) are used to sensitize polyoxometalates (POMs) with wide band gaps. Visible-light-induced photocatalytic reactions proceed through the formation of one-electron-reduced POMs, which also show photoenergy-storing properties (see figure).
  • Effect of Water Vapor on Pd-Loaded SnO2 Nanoparticles Gas Sensor, Nan Ma, Koichi Suematsu, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, ACS Applied Materials and Interfaces, 7, 5863, 5869,   2015年01月01日, 10.1021/am509082w, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84925353181&origin=inward
    概要:© 2015 American Chemical Society. The effect of water vapor on Pd-loaded SnO2 sensor was investigated through the oxygen adsorption behavior and sensing properties toward hydrogen and CO under different humidity conditions. On the basis of the theoretical model reported previously, it was found that the mainly adsorbed oxygen species on the SnO2 surface in humid atmosphere was changed by loading Pd, more specifically, for neat SnO2 was O-, while for 0.7% Pd-SnO2 was O2-. The water vapor poisoning effect on electric resistance and sensor response was reduced by loading Pd. Moreover the sensor response in wet atmosphere was greatly enhanced by loading Pd. It seems that the electron depletion layer by p-n junction of PdO-SnO2 may impede OH- adsorption. (Graph Presented).
  • Impurity level in SnO2 materials and its impact on gas sensing properties, R. G. Pavelko, R. G. Pavelko, M. Yuasa, M. Yuasa, T. Kida, K. Shimanoe, N. Yamazoe, Sensors and Actuators, B: Chemical, 210, 719, 725,   2015年01月01日, 10.1016/j.snb.2015.01.038, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84921966439&origin=inward
    概要:© 2015 Elsevier B.V. All rights reserved. Using the same protocol for precipitation of tin hydroxide and its hydrothermal treatment (HT), we synthesize SnO2 from three precursors - tin(IV) acetate, tin(IV) hydroxide acetate and tin(IV) chloride pentahydrate. After annealing on sensor substrates the materials were found to be very similar from structural point of view. However, their sensing properties (responses to CO and H2 as a function of humidity) were discovered to be very different, which was related to different impurity level in the samples. High amount of chlorine and potassium (ca. 300 ppmw) in two samples corresponded well to notably high water vapor effect. Differences in surface areas (within 20-60 m2/g) and pore volumes (between 0.11 and 0.19 cm3/g), found for the materials in question, seem to play minor role if the impurities are present.
  • Oxygen separation from air using Ba0.95La0.05FeO3-δ membranes fitted with porous La1-xSrxFeO3-δ layers, Tetsuya Kida, Subaru Ninomiya, Hiroki Tatsushiro, Ken Watanabe, Masayoshi Yuasa, Kengo Shimanoe, Ceramics International, 41, 7830, 7835,   2015年01月01日, 10.1016/j.ceramint.2015.02.118, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84927578324&origin=inward
    概要:© 2015 Elsevier Ltd. and Techna Group S.r.l. All rights reserved. Selective oxygen separation from air was performed using perovskite-type oxide membranes made of Ba0.95La0.05FeO3-δ. We demonstrated that surface modification of Ba0.95La0.05FeO3-δ membranes with La1-xSrxFeO3-δ catalyst layers led to an increase in oxygen permeation fluxes at 700-930 °C. We studied the effects of oxygen vacancy amounts, surface area, particles size, surface treatment of La1-xSrxFeO3-δ on the oxygen permeability of the membranes fitted with La1-xSrxFeO3-δ catalyst layers. Among the catalyst layers tested, the membranes fitted with La0.9Sr0.1FeO3-δ (x=0.1) showed the highest oxygen permeation flux probably because of its higher porosity and uniform morphology without open voids, which would increase the number of surface reaction sites. The obtained results suggest the feasibility of further upgrading the membrane performance by using surface catalyst layers having a homogeneous morphology and a different composition from that of the mother membrane.
  • Nanoparticle cluster gas sensor: Controlled clustering of SnO2 nanoparticles for highly sensitive toluene detection, Koichi Suematsu, Yuka Shin, Zhongqiu Hua, Kohei Yoshida, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, ACS Applied Materials and Interfaces, 6, 5319, 5326,   2014年04月09日, 10.1021/am500944a, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84898464388&origin=inward
    概要:Gas sensing with nanosized oxide materials is attracting much attention because of its promising capability of detecting various toxic gases at very low concentrations. In this study, using clustered SnO2 nanoparticles formed by controlled particle aggregation, we fabricated highly sensitive gas sensing films to detect large gas molecules such as toluene. A hydrothermal method using stanic acid (SnO2·nH2O) gel as a precursor produced monodispersed SnO2 nanoparticles of ca. 5 nm at pH 10.6. Decreasing the solution pH to 9.3 formed SnO2 clusters of ca. 45 nm that were assemblies of the monodispersed nanoparticles, as determined by dynamic light scattering, X-ray diffraction, and transmission electron microscopy analyses. Porous gas sensing films were successfully fabricated by a spin-coating method using the clustered nanoparticles due to the loose packing of the larger aggregated particles. The sensor devices using the porous films showed improved sensor responses (sensitivities) to H2 and CO at 300 °C. The enhanced sensitivity resulted from an increase in the film's porosity, which promoted the gas diffusivity of the sensing films. Pd loading onto the clustered nanoparticles further upgraded the sensor response due to catalytic and electrical sensitization effects of Pd. In particular, the Pd-loaded SnO2 nanoparticle clusters showed excellent sensitivity to toluene, able to detect it at down to low ppb levels. © 2014 American Chemical Society.
  • WO3 nanolamella gas sensor: Porosity control using SnO 2 nanoparticles for enhanced NO2 sensing, Tetsuya Kida, Aya Nishiyama, Zhongqiu Hua, Koichi Suematsu, Masayoshi Yuasa, Kengo Shimanoe, Langmuir, 30, 2571, 2579,   2014年03月11日, 10.1021/la4049105, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84896800173&origin=inward
    概要:Tungsten trioxide (WO3) is one of the important multifunctional materials used for photocatalytic, photoelectrochemical, battery, and gas sensor applications. Nanostructured WO3 holds great potential for enhancing the performance of these applications. Here, we report highly sensitive NO 2 sensors using WO3 nanolamellae and their sensitivity improvement by morphology control using SnO2 nanoparticles. WO 3 nanolamellae were synthesized by an acidification method starting from Na2WO4 and H2SO4 and subsequent calcination at 300 °C. The lamellae were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), which clearly showed the formation of single-crystalline nanolamellae with a c-axis orientation. The stacking of each nanolamella to form larger lamellae that were 50-250 nm in lateral size and 15-25 nm in thickness was also revealed. From pore size distribution measurements, we found that introducing monodisperse SnO2 nanoparticles (ca. 4 nm) into WO3 lamella-based films improved their porosity, most likely because of effective insertion of nanoparticles into lamella stacks or in between assemblies of lamella stacks. In contrast, the crystallite size was not significantly changed, even by introducing SnO2. Because of the improvement in porosity, the composites of WO3 nanolamellae and SnO2 nanoparticles displayed enhanced sensitivity (sensor response) to NO2 at dilute concentrations of 20-1000 ppb in air, demonstrating the effectiveness of microstructure control of WO3 lamella-based films for highly sensitive NO2 detection. Electrical sensitization by SnO2 nanoparticles was also considered. © 2014 American Chemical Society.
  • H2O/D2O exchange on SnO2 materials in the presence of CO: Operando spectroscopic and electric resistance measurements, Roman G. Pavelko, Joong Ki Choi, Atsushi Urakawa, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, Journal of Physical Chemistry C, 118, 2554, 2563,   2014年02月06日, 10.1021/jp4108766, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84893821531&origin=inward
    概要:Water isotope exchange in the presence of CO on two undoped tin dioxides has been studied using modulation excitation diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and resistance measurements at 300 C. Our results reveal that the material synthesized from tin tetrachloride (SnO2Cl) manifests higher affinity to chemisorbed water than that made from tin hydroxide acetate (SnO2Ac). The latter was shown to exhibit a strong correlation between the evolution of surface OH groups (bridging type, involved in hydrogen bonding) and electric resistance upon increasing concentration of CO. Water desorption kinetics, being independent of CO concentration for both materials, was found to be slower for SnO 2Cl by ca. 30% with respect to SnO2Ac. High affinity to water as well as low sensor signals to CO in humid air reported for SnO 2Cl were proposed to originate from traces of Cl ions (about 0.15 wt % for SnO2Cl and 0.03 wt % for SnO2Ac) and not microstructure, which has been confirmed to be similar for both materials. Two types of water adsorption and two CO sensing mechanisms are proposed for SnO2Cl and SnO2Ac on the basis of the results. © 2013 American Chemical Society.
  • Gas-sensing properties of p-type α-Fe2O3 polyhedral particles synthesized via a modified polyol method, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Yong Yang, Masayoshi Yuasa, Cao Minh Thi, Yanqin Cao, Thomas Nann, Masayuki Nogami, Masayuki Nogami, RSC Advances, 4, 8250, 8255,   2014年02月04日, 10.1039/c3ra46410e, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84893192437&origin=inward
    概要:The gas sensing properties of polyhedral α-Fe2O 3 particles were investigated. The polyhedral α-Fe 2O3 particles were synthesized via a modified polyol method with the addition of an extra amount of NaBH4 in ethylene glycol, and fabricated to a thick gas sensing film after calcination at 500°C and 900°C. The polyhedral α-Fe2O3 particles exhibited a p-type nature, which is a new result opposite to other results of recent reports of semiconductor gas sensors using α-Fe 2O3. In particular, we suggest that the difference between structure and morphology of α-Fe2O3 particles can lead to p-type and n-type characterization. In addition, we suggested that Na ions from NaBH4 were incorporated into α-Fe2O 3 oxide. They are the cause of the generation of holes in α-Fe2O3 oxide that led to the p-type nature of α-Fe2O3 oxide. The measurement of the sensor response to hydrogen, carbon monoxide, toluene, propane and ethanol revealed that the sensor device synthesized using polyhedral α-Fe2O 3 particles is sensitive to hydrocarbons and ethanol. Importantly, the sensor device using polyhedral α-Fe2O3 particles calcined at 900°C was strongly sensitive to ethanol due to the porous structure of the α-Fe2O3 particles. © 2014 The Royal Society of Chemistry.
  • Controlled synthesis and characterization of iron oxide nanostructures with potential applications for gas sensors and the environment, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Yong Yang, Masayoshi Yuasa, Cao Minh Thi, Yanqin Cao, Thomas Nann, Masayuki Nogami, Masayuki Nogami, RSC Advances, 4, 6383, 6390,   2014年01月22日, 10.1039/c3ra45925j, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84892561539&origin=inward
    概要:In the present research, large iron oxide microparticles with large sizes in the range of 1-5 μm have been facilely synthesized by a modified polyol method with NaBH4 as a versatile strong reducing agent. We found that the highly homogeneous iron oxide microparticles' novel structure is the best pure crystal phase of α-Fe2O3 in terms of polyhedral morphology and shape in existence. There are no diffraction peaks of other crystal phases from impurities in α-Fe2O3 microparticle products in the crystal growth. Interestingly, a new method of heat treatment or atomic surface deformation allowed for the discovery of a new large α-Fe2O3 structure with controlled specific α-Fe2O3 oxide grains in the crystal structure. The severe surface deformation of sharp, polyhedral, large α-Fe 2O3 microparticles under a sintering treatment was found to give un-sharp, polyhedral large α-Fe2O3 microparticles with specific grains and boundaries. © 2014 The Royal Society of Chemistry.
  • Solution-processed Cu2ZnSnS4 nanocrystal solar cells: Efficient stripping of surface insulating layers using alkylating agents, Satoshi Suehiro, Keisuke Horita, Kota Kumamoto, Masayoshi Yuasa, Tooru Tanaka, Katsuhiko Fujita, Kengo Shimanoe, Tetsuya Kida, Journal of Physical Chemistry C, 118, 804, 810,   2014年01月16日, 10.1021/jp408360j, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84892737139&origin=inward
    概要:Solution-processed photovoltaic (PV) devices based on semiconductor nanocrystals (NCs) such as Cu2ZnSnS4 (CZTS) and CuInS 2 (CIS) are attracting much attention for use in next-generation solar cells. However, the performance of NC-based devices is hindered by insulating surface-capping ligands that limit transfer/transport of charged carriers. Here, to remove surface-capping ligands (long-chain fatty amines) from NCs, we use the strong alkylating agent methyl iodide, which converts primary amines to quaternary amines that have low coordinating affinity to the NC surface. X-ray diffraction, Raman spectroscopy, and Fourier transform infrared spectroscopy analyses confirm the successful removal of capping ligands from the CZTS surface after treatment with methyl iodide without changing the crystal structure of CZTS. CZTS and CIS NC-based devices treated with methyl iodide exhibit a reproducible PV response under simulated sunlight. The developed route can potentially enhance the performance of NC-based devices used in a broad range of applications. © 2013 American Chemical Society.
  • Determination of oxygen adsorption species on SnO2: Exact analysis of gas sensing properties using a sample gas pretreatment system, Koichi Suematsu, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, Kengo Shimanoe, Journal of the Electrochemical Society, 161,   2014年01月01日, 10.1149/2.004406jes, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84904793512&origin=inward
    概要:Oxygen adsorption plays key roles in resistive-type SnO2 gas sensors that can very sensitively detect combustible gases such as CO and hydrocarbons. Thus, exact evaluation of the electric resistance of SnO 2 in response to oxygen is important to understand the oxygen adsorption mechanism. However, infinitesimal impurities contained in even high-grade commercial oxygen cylinders impose great effect on the sensitivity of SnO2. In this study, we designed an experimental system, which composed of gas pretreatment chambers including a Pt/Al2O3 combustion catalyst and a zeolite adsorbent, for exact analysis of gas sensing properties. Our experimental system allowed for the accurate determination of the dependence of the electrical resistance (R) on oxygen partial pressure (PO2) by removing impurities in sample gases. According to the linear correlation between R versus PO2 1/4, we concluded that oxygen adsorbed on the SnO2 surface in the form of O2- at 350 and 450°C in extremely dry conditions that was achieved using the experimental system. The competitive adsorption on the SnO2 surface in the form of O- and O2- was suggested at 300°C. © 2014 The Electrochemical Society.
  • H2O/D2O exchange in the presence of CO over SnO 2 nanomaterials: Operando DRIFTS and resistance study for gas sensor applications, R. G. Pavelko, J. K. Choi, A. Urakawa, M. Yuasa, T. Kida, K. Shimanoe, N. Yamazoe, Proceedings of SPIE - The International Society for Optical Engineering, 8811,   2013年12月09日, 10.1117/12.2026594, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84889042539&origin=inward
    概要:Modulation excitation diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) together with resistance measurements has been carried out to study water isotopic exchange on undoped SnO2 materials as a function of CO concentration. We compare two materials synthesized via hydrothermal treatment and different only in their precursors: SnO2 Ac synthesized from tin(IV) hydroxide acetate and SnO2 Cl from tin(IV) chloride pentahydrate. DRIFTS and resistance measurements were performed simultaneously in an environmental chamber at 300 °C and in a flow of humid air. The annealed materials were found to have similar particle sizes (16±7 nm), crystallite sizes (12±2 nm) and pore size distribution (9±1 nm). However, sensor tests showed notably higher responses to CO in the presence of water vapor for SnO2 Ac. Electronic effect of CO chemisorption quantitatively correlates with consumption of bridging hydroxyls on the latter surface upon increasing concentration of CO from 0 to 500 ppm in humid air. No such correlation was found for SnO2 Cl. Water desorption kinetics was found to be slower for the latter by ca. 30 % with respect to SnO2 Ac. Low activity of surface OH groups and consequently low sensor signals of SnO2 Cl were proposed to originate from traces of Cl ions found in the material after the synthesis despite negative Cl test before the hydrothermal treatment. © 2013 SPIE.
  • Photocatalytic recovery of noble metals from waste solutions using a polyoxometallate (POM)-based hybrid photocatalyst, Tetsuya Kida, Hiromasa Matsufuji, Masayoshi Yuasa, Kengo Shimanoe, Advanced Materials Research, 747, 518, 521,   2013年10月04日, 10.4028/www.scientific.net/AMR.747.518, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84884787782&origin=inward
    概要:We attempted the photo-chemical recovery of noble metals from solutions using inorganic-organic hybrid photocatalysts based on polyoxometallates (POMs) such as PMo12O40 3-, SiW12O40 4-, and γ-SiW10O36 8- coupled with a cationic surfactant, dimethyldioctadecylammonium (DODA). We also used γ-SiW10O36-O(SiC18H37)2 as a photocatalyst. The four different photocatalysts dissolved in chloroform successfully photoreduced gold ions dissolved in water in a two-phase (chloroform/water) system under UV irradiation (λ< 475 nm). The γ-SiW10O36/DODA photocatalyst exhibited the best activity and was able to recover gold from solution. It was suggested that one-electron reduced γ-SiW10O36 9-, which was formed by UV irradiation, reduced gold ions to produce large two-dimensional particles. The formation of sheet-like particles indicates that the reduction of gold ions occurred at the interface between chloroform and water. © (2013) Trans Tech Publications, Switzerland.
  • Pore and particle size control of gas sensing films using SnO2 nanoparticles synthesized by seed-mediated growth: Design of highly sensitive gas sensors, Tetsuya Kida, Shuhei Fujiyama, Koichi Suematsu, Masayoshi Yuasa, Kengo Shimanoe, Journal of Physical Chemistry C, 117, 17574, 17582,   2013年08月29日, 10.1021/jp4045226, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84883414628&origin=inward
    概要:Gas sensing is an important application of metal oxides. The gas sensor response of metal oxide films is greatly influenced by particle size, pore size, thickness, and surface states. To study the effects of particle and pore sizes of sensing films on sensitivity, we fabricated SnO2-based films with different particle and pore sizes and studied sensor responses to three different gases: H2, CO, and H2S with different Knudsen diffusion coefficients. The pore size radii of the gas sensing films were successfully controlled from 2.8 to 5.5 nm using SnO2 nanoparticles of different sizes (4-17 nm diameter) that were synthesized by seed-mediated growth under hydrothermal conditions. Sensor response to H2 increased with decreasing particle size because of the formation of an electron depletion layer within the nanosized crystals. In contrast, the response to CO and H 2S increased with increasing particle size and the resultant pore size. Using the Knudsen diffusion-surface reaction equation, we simulated a gas concentration profile within the films, which revealed that the diffusion of CO and H2S is limited by small pores because of their lower diffusion rates compared with H2. We show that controlling the pore size of the sensing films produces ultrasensitive films, and a large resistance change by 4 orders of magnitude is achieved in response to a low concentration of H 2S (5 ppm). © 2013 American Chemical Society.
  • Oxygen reduction activity of carbon-supported La1-xCa xMn1-yFeyO3 nanoparticles, Masayoshi Yuasa, Naoki Tachibana, Kengo Shimanoe, Chemistry of Materials, 25, 3072, 3079,   2013年08月13日, 10.1021/cm401276y, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84882238705&origin=inward
    概要:Carbon-supported La1-xCaxMn1-yFe yO3 nanoparticles were synthesized, and their oxygen reduction activities and electronic states were investigated. A reverse micelle method using KMnO4 as a source of high valence state Mn successfully yielded carbon-supported La1-xCaxMn1-yFe yO3 nanoparticles even when calcined under a reducing atmosphere. The oxygen reduction activity of carbon-supported La 1-xCaxMn1-yFeyO3 exceeded that of carbon-supported Pt nanoparticles when the Ca composition was limited to the range of 0.4 to 0.8. X-ray photoelectron spectroscopy (XPS) measurements of La1-xCaxMn1-yFeyO3 particle surfaces revealed the existence of Mn4+, which is important in the oxygen reduction activity. Depth analysis of La1-xCa xMn1-yFeyO3 nanoparticles by XPS revealed the formation of a CaCO3 impurity and an A-site deficient perovskite-type oxide containing a high surface concentration of Mn 4+. © 2013 American Chemical Society.
  • Discharge/charge characteristic of Li-air cells using carbon-supported LaMn0.6Fe0.4O3 as an electrocatalyst, Masayoshi Yuasa, Tsubasa Matsuyoshi, Tetsuya Kida, Kengo Shimanoe, Journal of Power Sources, 242, 216, 221,   2013年06月24日, 10.1016/j.jpowsour.2013.05.076, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84879097489&origin=inward
    概要:The discharge/charge performance of Li-air cell using the carbon-supported LaMn0.6Fe0.4O3 nanoparticle as a cathode catalyst was investigated in this study. The carbon-supported LaMn 0.6Fe0.4O3 nanoparticle was prepared via a reverse homogeneous precipitation method, and fabricated to air electrode. Li-air cell was constructed using air electrode, Li metal foil and 1.0 M LiPF6 in propylene carbonate as a cathode, anode and electrolyte, respectively. As the result, the carbon-supported LaMn0.6Fe 0.4O3 nanoparticle exhibited both the oxygen evolution activity and the oxygen reduction activity in the non-aqueous electrolyte. The investigation about the presence and absence of the catalytic layer and the gas diffusion layer revealed that each layer is indispensable for the excellent electrode performance, and that the catalytic layer and the gas diffusion layer has a important role to supply the electrolyte and the oxygen gas, respectively. The investigation about the amount of the catalytic layer and the effect of the oxygen concentration revealed that the oxygen diffusability into the air electrode strongly affects to the discharge capacity of Li-air cells. © 2013 Elsevier B.V. All rights reserved.
  • Catalytic combustion-type hydrogen sensor using BaTiO 3-based PTC thermistor, Masayoshi Yuasa, Takahito Nagano, Naoki Tachibana, Tetsuya Kida, Kengo Shimanoe, Journal of the American Ceramic Society, 96, 1789, 1794,   2013年06月01日, 10.1111/jace.12217, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84878692609&origin=inward
    概要:A catalytic combustion-type gas sensor using a positive temperature coefficient (PTC) thermistor, which shows a sharp resistance change around Curie temperature, was developed for the detection of hydrogen. La-doped BaTiO 3 (Ba0.998 La0.002 TiO3) was prepared through a solid-state method and an oxalic acid method. La-doped BaTiO3 obtained by the oxalic acid method showed improved PTC properties, due to the formation of fine particles, as compared to that prepared with the solid-state method. The resulting sensor device showed a fairly high H2 sensitivity in the range of 100-1000 ppm. In addition, the H 2 sensitivity and response speed were improved by coating a Pt/SiO2 catalyst on the sensor device because the catalytic combustion efficiency of H2 was improved by the catalyst coating. © 2013 The American Ceramic Society.
  • High sensitive gas sensor based on Pd-loaded WO3 nanolamellae, Zhongqiu Hua, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, Kengo Shimanoe, Thin Solid Films,   2013年05月17日, 10.1016/j.tsf.2013.04.088, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84877645920&origin=inward
    概要:An impregnation method has been proposed to prepare Pd-loaded WO3 nanolamellae for the gas sensing application. WO3 nanolamellae were synthesized via an acidification method and impregnated with H2Pd2Cl4 solution followed by an ammonia washing treatment. The microstructure and H2 sensing characteristics of the Pd-loaded WO3 nanolamellae were investigated. Electron microscopy studies revealed that PdO particles have been deposited on the surfaces of WO3 with a diameter ranging from 3 to 15 nm. With quite a small amount of Pd, the sensor resistivity was greatly enhanced and it demonstrated an extremely large response to the reduced gas. It was found that sensing response at low temperature increased dramatically with a rise in the gas concentration for Pd-loaded sensors. However, the sensor response at high temperature quickly saturated with increasing the H2 concentration for larger amount of Pd loading. An enhanced combustion effect of Pd and chemical adsorbed water could be responsible for such a saturation of sensing response at high temperatures. © 2013.
  • Synthesis and self-assembly of gold nanoparticles by chemically modified polyol methods under experimental control, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Nguyen Viet Long, Michitaka Ohtaki, Masayoshi Yuasa, Satoshi Yoshida, Taiga Kuragaki, Cao Minh Thi, Masayuki Nogami, Masayuki Nogami, Journal of Nanomaterials, 2013,   2013年04月05日, 10.1155/2013/793125, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84875652684&origin=inward
    概要:In our present research, bottom-up self-assembly of gold (Au) nanoparticles on a flat copper (Cu) substrate is performed by a facile method. The very interesting evidence of self-assembly of Au nanoparticles on the top of the thin assembled layer was observed by scanning electron microscopy (SEM). We had discovered one of the most general and simple methods for the self-assembly of metal nanoparticles. The general physical and chemical mechanisms of the evaporation process of the solvents can be used for self-assembly of the as-prepared nanoparticles. The important roles of molecules of the used solvents are very critical to self-assembly of the as-prepared Au nanoparticles in the case without using any polymers for those processes. It is clear that self-assembly of such one nanosystem of the uniform Au nanoparticles is fully examined. Finally, an exciting surface plasmon resonance (SPR) phenomenon of the pure Au nanoparticles in the solvent was fully discovered in their exciting changes of the narrow and large SPR bands according to synthesis time. The SPR was considered as the collective oscillation of valence electrons of the surfaces of the pure Au nanoparticles in the solvent by incident ultraviolet-visible light. Then, the frequency of light photons matches the frequency of the oscillation of surface electrons of the Au nanoparticles that are excited. © 2013 Nguyen Viet Long et al.
  • A micro gas sensor using TiO2 nanotubes to detect volatile organic compounds, Tetsuya Kida, Min Hyun Seo, Koichi Suematsu, Masayoshi Yuasa, Yuichi Kanmura, Kengo Shimanoe, Applied Physics Express, 6,   2013年04月01日, 10.7567/APEX.6.047201, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84880910406&origin=inward
    概要:To develop a portable gas sensor with low power consumption, we deposited a micro size sensing film (100 × 100 μm2) on a Si substrate with an integrated micro heater and electrodes constructed using micro-electro- mechanical system (MEMS) technology. TiO2 nanotubes ca. 500nm long with a 50 nm diameter were used to sense and detect volatile organic compounds (VOCs). We demonstrate that the MEMS sensor responded well to ethanol and toluene in air at elevated temperatures, such as 500 °C, which suggests that it is a promising battery-operable micro gas sensor for detecting VOCs. © 2013 The Japan Society of Applied Physics.
  • Efficient photorecovery of noble metals from solution using a γ-SiW10O36/surfactant hybrid photocatalyst, Tetsuya Kida, Hiromasa Matsufuji, Masayoshi Yuasa, Kengo Shimanoe, Langmuir, 29, 2128, 2135,   2013年02月19日, 10.1021/la3044347, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84874063636&origin=inward
    概要:In recent years, the recovery of noble metals from waste has become very important because of their scarcity and increasing consumption. In this study, we attempt the photochemical recovery of noble metals from solutions using inorganic-organic hybrid photocatalysts. These catalysts are based on polyoxometalates such as PMo12O40 3-, SiW 12O40 4-, and γ-SiW10O 36 8- coupled with a cationic surfactant, dimethyldioctadecylammonium (DODA). The three different photocatalysts dissolved in chloroform were successful in photoreducing gold ions dissolved in water in a two-phase (chloroform/water) system under UV irradiation (λ < 475 nm). The γ-SiW10O36/DODA photocatalyst exhibited the best activity and recovered gold from solution efficiently. It was suggested that one-electron reduced γ-SiW10O36 9- formed by the UV irradiation reduced gold ions. As a result, large two-dimensional particles (gold nanosheets) were produced using the γ-SiW10O36/DODA photocatalyst, indicating that the reduction of gold ions occurred at the interface between chloroform and water. The γ-SiW10O36/DODA photocatalyst was able to recover metals such as platinum, silver, palladium, and copper from deaerated solutions. The selective recovery of gold is possible by controlling pH and oxygen concentration in the reaction system. © 2013 American Chemical Society.
  • Preparation of nano-LaNiO 3 support electrode for rechargeable metal-air batteries, Masayoshi Yuasa, Hiroshi Imamura, Masatoshi Nishida, Tetsuya Kida, Kengo Shimanoe, Electrochemistry Communications, 24, 50, 52,   2012年10月01日, 10.1016/j.elecom.2012.08.015, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84865568682&origin=inward
    概要:We have already demonstrated that an air electrode using LaMnO 3-supported on LaNiO 3 efficiently works as a bi-functional air electrode for oxygen reduction and evolution. In order to improve the bi-functional activity, high specific surface area of nano-LaNiO 3 was prepared by a new route using ZnO particles as an aggregation inhibitor. Nano-sized LaNiO 3 (ca. 40 nm) was successfully prepared after removing ZnO by KOH solution from a LaNiO 3-ZnO mixture prepared by a reverse homogeneous precipitation (RHP) method. The result showed that increasing the surface area of LaNiO 3 support is very effective in improving both the oxygen reduction and evolution activities. © 2012 Elsevier B.V.
  • Preparation of a stable sol suspension of Pd-loaded SnO 2 nanocrystals by a photochemical deposition method for highly sensitive semiconductor gas sensors, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, ACS Applied Materials and Interfaces, 4, 4231, 4236,   2012年08月22日, 10.1021/am300941a, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84865272835&origin=inward
    概要:A stable sol suspension of Pd-loaded SnO 2 nanocrystals, which is valid for both fundamental studies of semiconductor gas sensor and fabrications of a micro gas sensor, was fabricated by the photochemical deposition of PdCl 4 2- onto SnO 2 in an aqueous solution. UV light was irradiated on a mixture of a SnO 2 sol obtained through a hydrothermal treatment of stannic acid gel in the presence of PdCl 4 2- and ethanol/water at pH 2. A stable sol suspension of Pd-loaded SnO 2 was successfully obtained by controlling the pH of the above suspension to 10.5 after UV irradiation. Thin-film type sensor devices (film thickness ∼200 nm) using Pd-loaded SnO 2 nanocrystal were successfully fabricated by a spin-coating method. Gas sensing measurements showed that the deposition of Pd on the SnO 2 nanocrystals resulted in large electrical sensitization effect. The maximum gas sensitization effect was obtained at 0.125 mol % Pd loading. Moreover, the Pd loading lowered the temperature, in which the maximum sensor response to H 2 was obtained, due to the efficient catalytic combustion of H 2 on Pd. © 2012 American Chemical Society.
  • Effects of crystallite size and donor density on the sensor response of SnO 2 nano-particles in the state of volume depletion, Koichi Suematsu, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, Kengo Shimanoe, Journal of the Electrochemical Society, 159,   2012年02月29日, 10.1149/2.107204jes, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84857418755&origin=inward
    概要:To verify theoretical model based on the surface depletion effect of oxide semiconductor in small crystallite, the SnO 2 particles of different crystallite size and donor density were prepared by controlling heat-treatment temperature and Fe 3+ doping concentration, respectively. In addition, Fe 3+-doped SnO 2 was compared with Fe 2O 3-loaded SnO 2 to discuss the effect of donor density. The electrical resistance and sensor response of prepared SnO 2 films were measured in various partial pressures of oxygen and hydrogen. As results, both undoped-and Fe 3+-doped SnO 2 showed the volume depletion in the oxygen concentration of more than 2.5% at 350°C. The dependence of electrical resistance on oxygen partial pressure for smaller crystallite had steeper slope. Furthermore Fe 3+-doping improved the sensor response to hydrogen, while the Fe 2O 3-loading did not work. Good agreement between experimental data the volume depletion theory was found. © 2012 The Electrochemical Society.
  • Combustion-type H2 gas sensor using a PTC thermistor based on Bi, Na-Codoped BaTiO3 as a transducer, Naoki Tachibana, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, Kengo Shimanoe, Sensor Letters, 9, 21, 25,   2011年12月15日, 10.1166/sl.2011.1411, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=83255192738&origin=inward
    概要:We investigated the H2 sensing properties of a catalytic combustion-type hydrogen sensor using a BaTiO3-based positive temperature coefficient (PTC) thermistor as a transducer. In this sensor, catalytic combustion of H2 on Pt electrodes or a catalyst layer induces a remarkable change in the electric resistance as a sensor signal when the operating temperature is set near the Curie temperature of BaTiO3 (120 °C). However, the sensor response to H2 is relatively low at lower H2 concentrations because of lower combustion efficiency near 120 °C. In this study, Ba0.9(Bi0.5Na 0.5)0.1Ti0.999Nb0.001O3 (BNN-BT) with a higher Curie temperature (146 °C) was used as a transducer to increase the operating temperature and thus improve the sensor response. The sensor using BNN-BT and a Pt/SiO2 combustion catalyst showed improved sensor responses particularly at lower H2 concentrations. It also showed good response and recovery behaviors in response to 100-1000 ppm H 2 in air. Copyright © 2011 American Scientific Publishers.
  • Enhanced gas sensing characteristics of Au-Loaded TiO2 Nanotube Sensors, Min Hyun Seo, Masayoshi Yuasa, Tetsuya Kida, Jeung Soo Huh, Noboru Yamazoe, Kengo Shimanoe, Sensor Letters, 9, 26, 30,   2011年12月15日, 10.1165/sl.2011.1412, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=81255133410&origin=inward
    概要:The loading of noble metals was carried out to enhance the gas sensing characteristics of TiO2 nanotube-based sensors. Using a photochemical deposition method, Au nanoparticles were successfully deposited on TiO 2 nanotubes prepared by a hydrothermal method in a highly-dispersed state. The sensor device using a porous film composed of the Au-loaded (0.5 wt%) TiO2 nanotubes exhibited improved sensor responses to 10-50 ppm toluene in air at 500 °C. The sensor response was about two times higher than that of a sensor using commercial TiO2 nanoparticles (degussa P-25). The results demonstrate that the Au loading is a very efficient method for improving the sensing characteristics of TiO2 nanotube-based sensors operative at high temperatures. Copyright © 2011 American Scientific Publishers.
  • Semiconductor gas sensor using nano-sized oxide for high-sensitive detection of environment-related gases, Kengo Shimanoe, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, 2011 IEEE Nanotechnology Materials and Devices Conference, NMDC 2011, 38, 43,   2011年12月01日, 10.1109/NMDC.2011.6155309, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84860490847&origin=inward
    概要:Semiconductor gas sensors are device consisting of sintered metal oxides, which can indicate target gas concentration by measuring the electric resistance of device. The gas sensors have been developed widely for detection of inflammable gases, toxic gases, odor gases, environmental-related gases and so on. As the materials, n-type oxides, such as SnO 2, In 2O 3, WO 3 and so on, are well known. For the material design of the semiconductor gas sensor, we have reported important three functions i.e. receptor function, transducer function and utility factor. In this presentation, the material design for high-sensitive detection of environmental-related gases is shown. © 2011 IEEE.
  • Gas sensor using noble metal-loaded TiO2 nanotubes for detection of large-sized volatile organic compounds, Min Hyun Seo, Masayoshi Yuasa, Tetsuya Kida, Yuich Kanmura, Jeung Soo Huh, Noboru Yamazoe, Kengo Shimanoe, Nippon Seramikkusu Kyokai Gakujutsu Ronbunshi/Journal of the Ceramic Society of Japan, 119, 884, 889,   2011年11月01日, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=81255177648&origin=inward
    概要:Detection of volatile organic compounds (VOCs) has attracted considerable attention for indoor air quality and human breath analysis. Here, resistive-type gas sensors with porous films made of Au-loaded TiO2 nanotubes were developed for the detection of large-sized VOCs. Well-dispersed Au nanoparticles (10 to 20 nm) were photo-chemically deposited on TiO2 nanotubes (80nm in diameter, 700nm in length) prepared by a hydrothermal method. The device using the Au-loaded TiO2 nanotubes showed improved sensor responses to ethanol and toluene (50 ppm) in air at 500°C. This suggested that Au nanoparticles deposited on the surface of TiO2 nanotubules without aggregation. We also demonstrated that the device could be used for the detection of largesized VOC molecule, i.e., 2,6-diisopropylphenol (propofol), an intravenously administered hypnotic drug for induction and maintenance of anesthesia. The Au-loaded TiO2 nanotubes would offer a way to continuously monitor a change in the concentration of VOCs in exhaled air for medical diagnostics. © 2011 The Ceramic Society of Japan.
  • Microstructure control of TiO2 nanotubular films for improved VOC sensing, Min Hyun Seo, Masayoshi Yuasa, Tetsuya Kida, Jeung Soo Huh, Noboru Yamazoe, Kengo Shimanoe, Sensors and Actuators, B: Chemical, 154, 251, 256,   2011年06月20日, 10.1016/j.snb.2010.01.069, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79955672208&origin=inward
    概要:Porous gas sensing films composed of TiO2 nanotubes were fabricated for the detection of volatile organic compounds (VOCs), such as alcohol and toluene. In order to control the microstructure of TiO2 nanotubular films, ball-milling treatments were used to shorten the length of TiO2 nanotubes and to improve the particle packing density of the films without destroying their tubular morphology and crystal structure. The ball-milling treatment successfully modified the porosity of the gas sensing films by inducing more intimate contacts between nanotubes, as confirmed by scanning electron microscopy (SEM) and mercury porosimetry. The sensor using nanotubes after the ball-milling treatment for 3 h exhibited an improved sensor response and selectivity to toluene (50 ppm) at the operating temperature of 500 °C. However, an extensive ball-milling treatment did not enhance the original sensor response, probably owing to a decrease in the porosity of the film. The results obtained indicated the importance of the microstructure control of sensing layers in terms of particle packing density and porosity for detecting large sized organic gas molecules. © 2010 Elsevier B.V. All rights reserved.
  • Durability of carbon-supported La-Mn-based perovskite-type oxides as oxygen reduction catalysts in strong alkaline solution, Masayoshi Yuasa, Noboru Yamazoe, Kengo Shimanoe, Journal of the Electrochemical Society, 158,   2011年04月29日, 10.1149/1.3551499, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79955153519&origin=inward
    概要:The durability of carbon-supported La-Mn-based perovskites for the oxygen reduction reaction in strong alkaline solutions was investigated. Carbon-supported perovskite-type oxide nanoparticles were prepared by using a reverse micelle method. The durability of the carbon-supported LaMnO3 nanoparticles was compared with that of carbon-supported LaMnO3 prepared by the mechanical mixing of LaMnO3 with the carbon support. As a result, the durability of the carbon-supported LaMnO3 nanoparticles was less than that of the carbon-supported LaMnO3 prepared by the mixing method due to a difference in the surface area of LaMnO3, which has an effect on the oxygen reduction reaction. In order to improve the durability of the carbon-supported LaMnO3 nanoparticles, Ca and Fe were substituted at the A-sites and B-sites of the perovskite lattice, respectively. As a result, it was found that the partial substitution of Ca and Fe is effective in improving the durability of LaMnO 3 under cathodic polarization in strong alkaline solutions. In particular, the substitution of Ca at the A-site not only improved the durability of the oxide but also enhanced the oxygen reduction activity owing to an increase in the average valence state of the B-sites of the perovskite lattice. © 2011 The Electrochemical Society.
  • Bi-functional oxygen electrodes using LaMnO3/LaNiO3 for rechargeable metal-air batteries, Masayoshi Yuasa, Masatoshi Nishida, Tetsuya Kida, Noboru Yamazoe, Kengo Shimanoe, Journal of the Electrochemical Society, 158,   2011年04月04日, 10.1149/1.3562564, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79953189710&origin=inward
    概要:Carbon supported-electrocatalysts are principally used as catalytic layers for air electrodes of metal air batteries. However, these types of air electrodes are problematic because the carbon support can be oxidized to water soluble organic compounds under anodic polarization for a charge process. In this study, we have investigated to use LaNiO3 as a possible electrode material to replace the carbon support because LaNiO3 has both high electric conductivity and high oxygen evolution activity. LaNiO 3 was prepared by a reverse homogeneous precipitation method, and then LaMnO3, which is active for oxygen reduction reactions, was successfully loaded onto the LaNiO3 by using a reverse micelle method. LaNiO3 had a much higher stability against anodic polarization as compared to carbon support. The LaMnO3/LaNiO 3 composite electrode showed excellent bi-functional oxygen reduction/evolution activity in an alkaline solution and this makes it a highly potential candidate for use in rechargeable metal-air batteries. © 2011 The Electrochemical Society.
  • High-performance oxygen reduction catalyst using carbon-supported La-Mn-based perovskite-type oxide, Masayoshi Yuasa, Kengo Shimanoe, Yasutake Teraoka, Noboru Yamazoe, Electrochemical and Solid-State Letters, 14,   2011年03月16日, 10.1149/1.3561762, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79952514049&origin=inward
    概要:To obtain a highly active and low-cost oxygen reduction electrode, as compared with a Pt-loaded carbon electrode, a nano-sized La-Mn-based perovskite-type oxide on a carbon support was prepared through the reverse-micelle method. An gas diffusion oxygen reduction electrode using nano-sized La0.4Ca0.6Mn0.9Fe 0.1O3 as a electrocatalyst allowed a electrode potential as high as -50 mV (vs HgHgO) in 9 moll NaOH at 500 mA cm-2. This electrode potential is much higher than the electrode potential of carbon-supported Pt nanoparticles at the same current density. This result suggests that nano-sized La0.4Ca0.6Mn0.9Fe 0.1O3 is a promising candidate as an alternative oxygen reduction catalyst of Pt nanoparticles. © 2011 The Electrochemical Society. All rights reserved.
  • C O2 sensor combining an MISiC capacitor and a binary carbonate, Hirofumi Inoue, Mike Andersson, Masayoshi Yuasa, Tetsuya Kida, Anita Lloyd Spetz, Kengo Shimanoe, Electrochemical and Solid-State Letters, 14,   2011年01月24日, 10.1149/1.3512998, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78751483299&origin=inward
    概要:A solid-state C O2 sensor device using a metal-insulator-silicon carbide (MISiC) capacitor combined with a Li2 C O3 -BaC O3 auxiliary layer was fabricated and tested for its basic sensing properties. The MISiC-based C O2 sensor attached with the carbonate showed typical capacitance-voltage (C-V) properties in air at 400°C, and the sensor device responded well to changes in C O2 concentration in air at 400°C. The sensor signals were directly proportional to the logarithm of C O2 concentration. The results suggested that an electrochemical reaction of C O2 occurred at the interface between the carbonate layer and the electrode, causing the applied voltage to shift in response to C O2. © 2010 The Electrochemical Society.
  • The enhancement of response speed by loading the noble metal into the sensing layer for FET-Type N O2 sensors, Hirofumi Inoue, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, Kengo Shimanoe, Journal of the Electrochemical Society, 158,   2011年01月05日, 10.1149/1.3525625, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78650754851&origin=inward
    概要:In order to enhance the response speed, noble metal (Ru) loading into the W O3-NaN O2 sensing layer for the field effect transistor (FET)-based N O2 sensors was investigated. The sensing layer was prepared by heat-treating the mixture powder of NaN O2 and noble metal (Ru)-loaded W O3 at 300°C. The effects of loading amounts of the noble metal on N O2 sensing performances as well as the microstructure of the sensing layer have been examined. It was found that the optimization of the noble metal loading amount into the sensing layer was important for the improvement of 90% response-and recovery-times. Field emission scanning electron microscopy observations revealed that the sensing layer became porous with increasing noble metal loading amounts. However, extensive addition of Ru (above 0.2 wt % to W O3) into the sensing layer resulted in the degradation of sensing characteristics, although the sensing layer showed a highly porous structure. According to theoretical analysis based on Knudsen gas diffusion reported by Matsunaga, the diffusion of gas molecules into such a porous sensing layer is very fast. Therefore the obtained results suggested that the improvement of the response-and recovery-speeds is owing to the large contribution of noble metal nanoparticle to the electrochemical promotion rather than the diffusion of N O2 gas into the sensing layer. © 2010 The Electrochemical Society.
  • Microstructure effect on the oxygen permeation through Ba 0.95La0.05FeO3-δ membranes fabricated by different methods, Ken Watanabe, Subaru Ninomiya, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, Hajime Haneda, Kengo Shimanoe, Journal of the American Ceramic Society, 93, 2012, 2017,   2010年07月01日, 10.1111/j.1551-2916.2010.03700.x, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77953787945&origin=inward
    概要:In order to investigate the effect of the microstructure on the oxygen permeation in Ba0.95La0.05FeO3-δ membranes, three different methods such as solid-state reaction, nitrate and acetate decomposition (NAD), and amorphous malic acid precursor (AMP) methods were used to fabricate membranes with different grain sizes. The grain size of the membranes was successfully controlled from 35 to 829 μm2 via sintering at 1175°-1275°C. The oxygen permeation fluxes through the Ba0.95La0.05FeO3-δ membranes increased with a decrease in the grain size. The AMP method, using malic acid as a complexing agent, produced a membrane having the highest oxygen permeability (3.10 cm3·(min·cm2)-1 at 930°C) and the smallest grain size. The results obtained again confirmed the significant importance of microstructure control in designing high-performance oxygen permeable membranes. © 2010 The American Ceramic Society.
  • High-performance oxygen-permeable membranes with an asymmetric structure using Ba0.95La0.05FeO3-δ perovskite-type oxide, Ken Watenabe, Masayoshi Yuasa, Tetsuya Kida, Yasutake Teraoka, Noboru Yamazoe, Kengo Shimanoe, Advanced Materials, 22, 2367, 2370,   2010年06月04日, 10.1002/adma.200903953, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77953140408&origin=inward
    概要:(Figure Presented) High oxygen permeability was achieved using an asymmetric Ba0.95La0.05FeO3-δ membrane. In this membrane, oxygen diffuses physically through pores of a porous support and oxygen permeates electrochemically through a dense layer. The oxygen permeation flux of the asymmetric Ba0.95La0.05FeO 3-δ membrane reached more than 10 cm3 (STP) min -1 cm-2 from a test gas containing 50% oxygen at 930°C. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
  • Structural optimization of gas diffusion electrodes loaded with LaMnO 3 electrocatalysts, Masayoshi Yuasa, Akiko Koga, Tetsuya Kida, Kengo Shimanoe, Noboru Yamazoe, Journal of Applied Electrochemistry, 40, 675, 681,   2010年03月01日, 10.1007/s10800-009-0042-9, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77949265452&origin=inward
    概要:In this study, gas diffusion electrodes (GDEs) with two catalyst layers were fabricated and tested for their electrode performance for oxygen reduction in an alkaline solution. The LaMnO3/carbon black catalyst layers were fabricated using a reverse micelle method to finely disperse the LaMnO 3 particles onto the carbon matrices, for which commercial Ketjen Black (KB) (1270 m2 g-1) and Vulcan XC-72R (VX) (254 m2 g-1) were used. The three-layer-structured GDE with the two LaMnO3/KB and LaMnO3/VX catalyst layers exhibited a superior oxygen reduction activity when compared to that of a conventional GDE with only one LaMnO3/KB catalyst layer. Pore size distribution and gas permeability measurements revealed that the LaMnO3/VX layer was more porous and had higher gas permeability than the LaMnO3/KB layer. These results suggest that the intermediate layer of LaMnO3/VX can efficiently supply oxygen to reaction sites dispersed in the LaMnO 3/KB and LaMnO3/VX catalyst layers, which consequently leads to an improvement in the electrode performance. © 2009 Springer Science+Business Media B.V.
  • Wet process-preparation of Re-doped WO3 for wide range of NO2 detection, Masayoshi Yuasa, Yoshiyuki Matoba, Yoshiyuki Matoba, Noboru Yamazoe, Kengo Shimanoe, Nippon Seramikkusu Kyokai Gakujutsu Ronbunshi/Journal of the Ceramic Society of Japan, 118, 184, 187,   2010年03月01日, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77949498317&origin=inward
    概要:In order to reduce the electric resistance of the WO3 sensing film fabricated from the ion-exchange method, lamellar-structured and Re-doped WO3 was prepared through the acidification method. The mixed solution of Na2WO4 and Re2O7 was dropped into the mixed solution of H2SO4 and HCHO. Then the obtained gel was deposited on alumina substrate with Au electrode for thick film devices and calcined at 300°C. The size of the Re-doped WO3 particles was smaller in one order in magnitude than that of the WO3 by the ion-exchange method. The electric resistance of Re-doped WO3 device in air showed minimum value at the 4 at% Re doping due to the increase in the donor density in the WO3 crystal. As a result, the Re-doped WO3 device exhibited low electric resistance less than 108 Ω even in the 800 ppb NO2. Such a low electric resistance device is suitable for the detection of the wide range of NO2. © 2010 The Ceramic Society of Japan.
  • Oxygen permeation properties of partially A-site substituted BaFe O3-δ perovskites, Tetsuya Kida, Daisuke Takauchi, Ken Watanabe, Masayoshi Yuasa, Kengo Shimanoe, Yasutake Teraoka, Noboru Yamazoe, Journal of the Electrochemical Society, 156,   2009年11月10日, 10.1149/1.3231690, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=70350738275&origin=inward
    概要:To explore oxygen permeable materials, oxygen permeation properties of partially A-site substituted BaFe O3-δ perovskites were investigated. Ba sites in BaFe O3-δ were substituted with cations such as Na, Rb, Ca, Y, and La by 5%. The partial substitution with Ca, Y, and La, whose ionic radii are smaller than that of Ba, succeeded in stabilizing a cubic perovskite structure that is a highly oxygen permeable phase, as revealed by X-ray diffraction analysis. This can be explained in terms of a decrease in the tolerance factor (t). Among the Ba0.95 M 0.05 Fe O3-δ (M = Na, Rb, Ca, Y, and La) membranes tested, Ba0.95 La0.05 Fe O3-δ showed the highest oxygen permeability at 600-930°C, owing to the stabilization of the cubic phase without the formation of impurity phases. From chemical analysis, the oxygen permeability of Ba1-x Lax Fe O 3-δ membranes was correlated with the amount of oxygen defects (δ) in the lattice. The oxygen permeation flux of Ba0.95 La0.05 Fe O3-δ membrane was significantly increased by reducing its thickness. Furthermore, a Ba0.975 La0.025 Fe O3-δ membrane exhibited good phase stability under He flow at elevated temperatures. The obtained results indicate the promising properties of Ba1-x Lax Fe O3-δ membranes as a cobalt-free material that has a high oxygen permeability, good phase stability, and low cost. © 2009 The Electrochemical Society.
  • Glass-coated mixed conducting cobaltites as solid-reference electrode materials for NASICON-based potentiometric CO2 sensors, Shotaro Kishi, Yuji Miyachi, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, Noboru Yamazoe, Journal of the Electrochemical Society, 156,   2009年10月13日, 10.1149/1.3216044, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=70349754513&origin=inward
    概要:To improve the stability of Na3Zr2Si 2PO12 (NASICON)-based potentiometric CO2 sensors fitted with carbonate/Au layers (sensing electrode), mixed conducting oxides of Li0.4CoO2 and Na0.6CoO2 were examined for their applicability to solid-reference electrodes in terms of their stability against CO2 and humidity. Compared with the Na 0.6CoO2 electrode, the Li0.4CoO2 electrode showed far better stability against CO2. When the Li 0.4CoO2 electrode was coated with a layer of glass, the electrode showed no response to CO2 (200-2000 ppm) and little interference from humidity [21-86% relative humidity (RH)] at 450°C. A CO2 sensor device using Li2CO3-BaCO3 and a glass-coated Li0.4CoO2 showed stable electromotive force (emf) responses to CO2 in humid air (86% RH) at 450°C. The emf of the device was also stable even after it was exposed to humid air (86% RH) containing CO2 (400 ppm) at room temperature for 1-2 days. The present study indicates the promising features of the glass-coated Li 0.4CoO2 as a stable solid-reference material for NASICON-based CO2 sensors. © 2009 The Electrochemical Society.
  • Detection of organic gases using TiO2 nanotube-based gas sensors, Min Hyun Seo, Masayoshi Yuasa, Tetsuya Kida, Jeung Soo Huh, Noboru Yamazoe, Kengo Shimanoe, Procedia Chemistry, 1, 192, 195,   2009年09月01日, 10.1016/j.proche.2009.07.048, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=71549153470&origin=inward
    概要:We fabricated porous gas sensing films composed of TiO2 nanotubes prepared by a hydrothermal treatment for the detection of organic gases, such as alcohol and toluene. The morphology of the sensing films was controlled with a ball-milling treatment and calcination at high temperature to improve the sensitivity of the films. The sensor using nanotubes with the ball-milling treatment exhibited the improved sensor responses to toluene at 500oC. The results obtained indicated the importance of the microstructure control of sensing layers in terms of particle packing density, pore size distribution, and particle size and shape for detecting large sized organic gas molecules. © 2009.
  • Microstructure control of WO 3 film by adding nano-particles of SnO 2 for NO 2 detection in ppb level, Kengo Shimanoe, Aya Nishiyama, Masayoshi Yuasa, Tetsuya Kida, Noboru Yamazoe, Procedia Chemistry, 1, 212, 215,   2009年09月01日, 10.1016/j.proche.2009.07.053, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=71549173713&origin=inward
    概要:To fabricate more excellent NO 2 sensor with high sensor response and good linearity between the sensor response and NO 2 concentration, the microstructure of WO 3 lamellae was controlled by adding nano-particles of SnO 2. It was found that the sintering of WO 3 lamellae was inhibited by adding nano-particles of SnO 2. The device using WO 3 lamellae added a small amount of SnO 2 nano-particles had the highest sensor response, exhibiting a high sensor response (S = 60-540) even to dilute NO 2 (100-1000 ppb) in air at 200°C. © 2009.
  • Oxygen permeation of a dense/porous asymmetric membrane using La 0.6 Ca 0.4 CoO 3-δ-BaFe 0.975 Zr 0.025 O 3-δ system, Ken Watanabe, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, Yasutake Teraoka, Noboru Yamazoe, Chemistry Letters, 38, 94, 95,   2009年07月20日, 10.1246/cl.2009.94, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=67650489156&origin=inward
    概要:To achieve a high oxygen permeation rate at medium and high temperature, an asymmetrically structured membrane, in which a thin dense layer (30μm) made of La 0.6Ca 0.4CoO 3-δ (LCC) and BaFe 0.975Zr 0.025O 3-δ (BFZ) was formed on a porous LCC support, was fabricated and tested for its oxygen permeability. The oxygen permeation flux significantly increased by mixing BFZ with LCC and reached a fairly high value of 1.60 cm 3 min -1 cm -2 even at 780°C. Copyright © 2009 The Chemical Society of Japan.
  • Oxygen permeation properties of Co-free perovskite-type oxide membranes based on BaFe 1-yZr yO 3-δ, Ken Watanabe, Daisuke Takauchi, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, Yasutake Teraoka, Noboru Yamazoe, Journal of the Electrochemical Society, 156,   2009年04月08日, 10.1149/1.3086763, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=63649099847&origin=inward
    概要:Partially Zr-substituted BaFe 1-yZr yO 3-δ membranes were developed as a Co-free oxygen permeable membrane. In order to stabilize the cubic perovskite structure, Fe sites in BaFeO 3-δ were partially substituted with Zr 4+. In the substitution range of y=0.01-0.1, the cubic perovskite structure was stabilized even at room temperature. Among the membranes prepared, a BaFe 0.975Zr 0.025O3 -δ material (y=0.025) showed the highest oxygen permeation flux of 1.30 cm3 (standard temperature pressure) min-1 cm-2 at 930°C under an air/He gradient. The oxygen permeation flux was higher than that of partially Ce-substituted BaFe 1-yCe yO 3-δ membranes reported previously. From the results obtained by chemical and scanning electron microscope analyses, it appears that the oxygen permeability for BaFe 1-yZr yO 3-δ membranes was well correlated with the amount of oxygen defects in the lattice as well as the grain size. In addition, the oxygen permeation flux of the BaFe 0.975Zr 0.025O3 -δ membrane was significantly increased after decreasing the thickness of the membrane from 2.0 to 0.4 mm. For thin membranes (0.4-1.0 mm), the thickness dependence of the oxygen permeability deviated from the Wagner equation, suggesting that the oxygen permeation of BaFe 0.975Zr 0.025O3 -δ is controlled by not only bulk diffusion of oxide ions but also their surface reactions. © 2009 The Electrochemical Society.
  • Gas sensing characteristics and porosity control of nanostructured films composed of TiO2 nanotubes, Min Hyun Seo, Masayoshi Yuasa, Tetsuya Kida, Jeung Soo Huh, Kengo Shimanoe, Noboru Yamazoe, Sensors and Actuators, B: Chemical, 137, 513, 520,   2009年04月02日, 10.1016/j.snb.2009.01.057, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=62649120085&origin=inward
    概要:Preparation and morphology control of TiO2 nanostructured films for gas sensor applications were investigated. To examine the effect of the morphology of sensing films on the sensing characteristics, TiO2 with different morphologies, nanoparticles and nanotubes, were used for the film preparation. TiO2 nanotubes were prepared by a hydrothermal treatment of TiO2 nanoparticles in a NaOH solution at 160, 200, and 230 °C for 24 h and subsequent washing with an HCl solution. Uniform sized TiO2 nanotubes of 1 μm in length and 50 nm in diameter were formed at 230 °C. The sensing films composed of nanotubes prepared at 230 °C showed a high sensor response to toluene at 500 °C as compared with those composed of TiO2 nanoparticles. Scanning electron microscope (SEM) analysis and pore size distribution measurements indicated that the sensing films composed of the TiO2 nanotubes had a high porous morphology with a peak pore size of around 200 nm, which can promote the diffusion of toluene deep inside the films and improve the sensor response. The obtained results demonstrated the importance of microstructure control of sensing layers for improving the sensitivity to large size molecules like volatile organic compounds (VOCs). © 2009 Elsevier B.V. All rights reserved.
  • Planar-type BiCuVOx solid electrolyte sensor for the detection of volatile organic compounds, Tetsuya Kida, Takuya Minami, Shotaro Kishi, Masayoshi Yuasa, Kengo Shimanoe, Noboru Yamazoe, Sensors and Actuators, B: Chemical, 137, 147, 153,   2009年03月28日, 10.1016/j.snb.2008.12.014, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=60549108719&origin=inward
    概要:Mixed potential-type gas sensors with a BiCuVOx (Bi2Cu0.1V0.9O5.35) oxygen conductor, fitted with composite electrodes made of perovskite-type oxide (La0.6Sr0.4Co0.8Fe0.2O3) and BiCuVOx, were tested for their organic gas sensing properties. A planar-type BiCuVOx-based device, in which thin sensing electrode and thick counter electrode are attached, exhibited good sensing characteristics to low ethanol concentrations (4-30 ppm) at 400 °C. The electromotive force (EMF) of the device had a linear relation to the logarithm of ethanol concentration. The 90% response and recovery times of the device were short, i.e., less than 1 min. Moreover, the planar structure successfully eliminated any oxygen interference. The ethanol sensing mechanism is based on the mixed potential generation from the simultaneous anodic oxidation of ethanol and the cathodic reduction of oxygen, at the BiCuVOx/electrode interface. © 2008 Elsevier B.V. All rights reserved.
  • Nano-sized PdO loaded SnO2 nanoparticles by reverse micelle method for highly sensitive CO gas sensor, Masayoshi Yuasa, Takanori Masaki, Tetsuya Kida, Kengo Shimanoe, Noboru Yamazoe, Sensors and Actuators, B: Chemical, 136, 99, 104,   2009年02月02日, 10.1016/j.snb.2008.11.022, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=58249144823&origin=inward
    概要:A reverse micelle method was investigated for preparing nano-sized PdO loaded on SnO2 nanoparticles. PdO-SnO2 nano-composite was prepared by precipitating Pd(OH)2 and Sn(OH)4 inside a reverse micelle. The microstructure and the gas sensing properties of obtained nanoparticles were investigated. Although the particle size of SnO2 was as same as ca. 10 nm at each observed sample, the particle size of PdO got larger as increasing with loading amount of PdO because of agglomeration of PdO nanoparticles each other. As a result of the gas sensing measurement, it was found that the particle size of PdO on SnO2 nanoparticle influences the gas sensing property closely. That is, the sensor response declined gradually with increasing the particle size of PdO although the maximum of the sensor response was obtained in PdO = 0.1 mol%. In this method, small amount of PdO loading can be achieved as compared with PdO-loaded SnO2 sensor prepared by the conventional impregnation method. © 2008 Elsevier B.V. All rights reserved.
  • Highly sensitive NO2 sensors using lamellar-structured WO3 particles prepared by an acidification method, Tetsuya Kida, Aya Nishiyama, Masayoshi Yuasa, Kengo Shimanoe, Noboru Yamazoe, Sensors and Actuators, B: Chemical, 135, 568, 574,   2009年01月15日, 10.1016/j.snb.2008.09.056, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=57949113496&origin=inward
    概要:Tungsten trioxide (WO3) was prepared by acidification of Na2WO4 with acid solutions such as H2SO4, HCl, and HNO3 (pH 0.5 to -0.8) and tested for its NO2 sensing properties. Acidification with strong acid solutions (pH -0.5, -0.8) was found to produce lamellar-structured WO3 particles, which consisted of nano-sized crystalline plates that were 100-350 nm in lateral size and 20-50 nm in thickness, as observed by XRD and SEM analyses. The sizes of the primary and secondary particles were decreased by decreasing the pH of the acid solution used. This was accompanied by an increase in the specific surface area. The NO2 responses of the prepared WO3 lamellae were dependent on their morphology. The device using smaller WO3 lamellae prepared with a H2SO4 solution (pH -0.8) had the highest sensor response, exhibiting a high sensor response (S = 150-280), even to dilute NO2 (50-1000 ppb) in air at 200 °C. The use of smaller lamellae resulted in a decrease in the electrical resistance of the device, probably due to intimate contact between smaller lamellar particles, which allowed the detection of NO2 in a rather wide concentration range. In addition, the developed device showed high NO2 selectivity without substantial interference from NO. © 2008 Elsevier B.V. All rights reserved.
  • Effect of preparation routes on the catalytic activity over SmFeO3 oxide, Masami Mori, Yuji Iwamoto, Makiko Asamoto, Yoshiteru Itagaki, Hidenori Yahiro, Yoshihiko Sadaoka, Satoko Takase, Youichi Shimizu, Masayoshi Yuasa, Kengo Shimanoe, Hajime Kusaba, Yasutake Teraoka, Catalysis Today, 139, 125, 129,   2008年12月15日, 10.1016/j.cattod.2008.08.014, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=54849413775&origin=inward
    概要:The perovskite-type SmFeO3 powders were prepared by the four different methods, named decomposition method of heteronuclear cyano complexes (CN), polymer precursor method (PP), reverse micelle method (RM) and reverse homogenous precipitation method (RHP), and their catalytic activities were evaluated with a CO oxidation reaction. The surface areas and the surface chemical compositions of Sm, Fe, O and C were strongly dependent on the preparation methods and calcination temperatures. On the basis of such the characteristics on the surface the factors controlling the catalytic activity are discussed. © 2008 Elsevier B.V. All rights reserved.
  • Exploration of new sensing electrode materials for FET-type NOx sensors with fast response, H. Inoue, M. Yuasa, T. Kida, K. Shimanoe, N. Yamazoe, Sensor Letters, 6, 912, 915,   2008年12月01日, 10.1166/sl.2008.528, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=63049099002&origin=inward
    概要:A FET type NO2 sensor fitted with NaNO2-RU/WO3 as a new auxiliary (sensing) layer was fabricated and tested for its NO2 sensing properties. The developed device responded to dilute NO2 of ppb concentrations (20-300 ppb) at 130 and 170 °C. The sensor signal (VGs; gate-source voltage) is linearly proportional to the logarithm of NO2 concentration, exhibiting the Nernstian response. It was found that the response speed was improved at lower operating temperature by adding Ru to the NaNO2-WO3 auxiliary layer. It was suggested that Ru nanoparticles deposited in the auxiliary layer with a porous morphology improved the rate of adsorption and electrochemical reaction of NO2 occurring at the interface between the Au gate electrode and auxiliary layer. Copyright © 2008 American Scientific Publishers All rights reserved.
  • Dense/porous asymmetric-structured oxygen permeable Membranes based on la0.6Ca0.4CoO3 perovskite-type oxide, Ken Watanabe, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, Yasutake Teraoka, Noboru Yamazoe, Chemistry of Materials, 20, 6965, 6973,   2008年11月25日, 10.1021/cm8013144, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=57649111998&origin=inward
    概要:To achieve high-efficiency oxygen permeation using mixed (ionic and electronic) conducting perovskite-type oxides, we examined asymmetric-structured membranes of La0.6Ca0.4CoO3 in which a thin dense membrane was deposited on a porous support. The La0.6Ca 0.4CoO3 porous support was fabricated using irregular-shaped precursor particles prepared through an oxalate method. The fabricated support had good gas permeability and thermal stability, showing sufficient properties as a support for dense thin membranes. A dense membrane of 10 μm thickness was successfully formed on the porous support by coating a La0.6Ca0.4CoO3 slurry and subsequent densification by sintering. The deposited thin membrane was gastight and free from clacks, as revealed by gas permeation tests and SEM observations. The asymmetric membrane exhibited a high oxygen permeability of 1.66 cm3 (STP, standard temperature and pressure) min-1 cm-2 at 930 °C, which was four times higher than that of a typical sintered-disk type membrane with 1200 μm thickness, demonstrating its feasibility as a high-performance oxygen separation membrane. © 2008 American Chemical Society.
  • Deposition of Pd onto SnO2 nanoparticles-based gas sensors using a Pd complex as the precursor, Tetsuya Kida, Hiroyuki Kurachi, Masayoshi Yuasa, Kengo Shimanoe, Noboru Yamazoe, Advanced Materials Research, 47-50 PART 2, 1506, 1509,   2008年11月24日, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=56349156742&origin=inward
    概要:The deposition of Pd nanoparticles onto thiol-functionalized SnO 2 nanoparticles was carried out at the aqueous/organic liquid/liquid interface to prepare Pd-loaded SnO2 nanoparticles for high-sensitive sensor materials. The method is based on the self-assembly deposition of Pd onto dimercaptosucinic acid (DMSA)-functionalized SnO2 nanoparticles (mean diameter: 4 nm) prepared by a hydrothermal method. Pd nanoparticles of 2-3 nm in chloroform were prepared by thermal decomposition of a Pd complex at high temperature (170°C). Thin film-type device using the prepared Pd-loaded SnO2 nanoparticles was fabricated and tested for its sensing properties. © 2008 Trans Tech Publications.
  • Effect of foreign metal doping on the gas sensing behaviors of SnO 2-based gas sensor, Kouichi Suematsu, Takanori Honda, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, Noboru Yamazoe, Advanced Materials Research, 47-50 PART 2, 1502, 1505,   2008年11月24日, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=56349104834&origin=inward
    概要:Recently, we have proposed some theoretical models, power laws and effect of particle shape and size, for semiconductor gas sensors. The models show that a depletion theory of semiconductor can be combined with the dynamics of adsorption and/or reactions of gases on the surface. In the case of SnO 2, the relative resistance (R/R0) is proportional to PO2 n, where n is a constant value (n=1/2) on oxygen partial pressure. In addition, carrier concentration in SnO2 influences depth of the depletion. In this study, to experimentally reveal such effects, we tried to control the carrier concentration in SnO2 by foreign doping and examined their electrical resistance and sensor response. Correlations between doping concentration, crystalline size, and partial pressures of oxygen and H2 on the electric resistance are discussed to reveal the material design for semiconductor gas sensors. © 2008 Trans Tech Publications.
  • Preparation of oxygen evolution layer/La0.6Ca0.4CoO3 dense membrane/porous support asymmetric structure for high-performance oxygen permeation, Ken Watanabe, Masayoshi Yuasa, Tetsuya Kida, Kengo Shimanoe, Yasutake Teraoka, Noboru Yamazoe, Solid State Ionics, 179, 1377, 1381,   2008年09月30日, 10.1016/j.ssi.2007.12.092, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=48349096486&origin=inward
    概要:An asymmetric-structured membrane, in which a dense thin La0.6Ca0.4CoO3 layer of 10 μm was deposited on porous La0.6Ca0.4CoO3 support by a slurry dropping method, were tested for its oxygen permeability at 630-930 °C. In order to increase the oxygen permeability, porous La0.6Ca0.4CoO3 and SrCo0.8Fe0.2O3 - δ oxygen evolution layers were attached on the dense layer. It was found that the asymmetric structured membranes with the porous oxygen evolution layers showed remarkably higher oxygen permeability as compared with a conventional sintered disk-type membrane (1200 μm). This suggests that oxygen permeation through membranes of 10 μm in thickness is rate-determined by both bulk O2- diffusion and oxygen evolution reaction. The maximum oxygen permeability reached 4.77 cm3 (STP) min- 1 cm- 2 (3.54 × 10- 6 mol cm- 2 s- 1) at 930 °C for the asymmetric membrane with porous La0.6Ca0.4CoO3 oxygen evolution layer of 10 μm in thickness (STP = Standard Temperature and Pressure). Further improvements in the oxygen permeability would be achieved through control of the micro-structure of the oxygen evolution layers. © 2008 Elsevier B.V. All rights reserved.
  • Study on the response and recovery properties of semiconductor gas sensors using a high-speed gas-switching system, Tetsuya Kida, Toru Kuroiwa, Masayoshi Yuasa, Kengo Shimanoe, Noboru Yamazoe, Sensors and Actuators, B: Chemical, 134, 928, 933,   2008年09月25日, 10.1016/j.snb.2008.06.044, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=51649126606&origin=inward
    概要:A high-speed gas-switching system, in which a low-dead volume chamber (0.6 cm3) was connected to a gas flow apparatus equipped with a high-speed gas-switching valve operative at a rate of 30 ms, was designed to investigate the real response and recovery properties of semiconductor gas sensors. The developed system allowed rapid replacement of the gas atmosphere in the chamber where a gas sensor device was placed within 0.3 s. It was revealed that the response speed of the sensor device based on a SnO2 porous film (pore size at maximum population: 37 nm) was remarkably fast, reaching a response time of less than 1 s for H2 and CO detection at 250 and 350 °C. This suggests that the diffusion and surface reaction of H2 and CO are quite fast in the porous film. On the other hand, the recovery speed was not comparably fast and the resistance of the device did not recover to the original state within 20 s after switching the gas atmosphere in the chamber from the sample gases to air. This is possibly due to the slow desorption of the H2O and CO2 that were formed by the surface reaction of H2 and CO, respectively with the adsorbed oxygen on SnO2. © 2008 Elsevier B.V. All rights reserved.
  • Planar NASICON-based CO2 sensor using BiCuVOx /Perovskite-type oxide as a solid-reference electrode, Tetsuya Kida, Tetsuya Kida, Shotaro Kishi, Masayoshi Yuasa, Kengo Shimanoe, Kengo Shimanoe, Noboru Yamazoe, Noboru Yamazoe, Journal of the Electrochemical Society, 155,   2008年04月14日, 10.1149/1.2889011, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=41849122337&origin=inward
    概要:To improve the stability of a NASICON (Na3 Zr2 Si2 PO12; Na+ conductor)-based potentiometric CO2 sensor under humid conditions, a composite of BiCuVOx (Bi2 Cu0.1 V0.9 O5.35) and perovskite-type oxide (La0.6 Sr0.4 Co0.78 Ni0.02 Fe0.2 O3) was used as a solid-reference electrode. The CO2 sensing properties and stability of a NASICON-based planar device fitted with Li2 CO3 - BaCO3 (auxiliary phase) and the composite reference electrode were examined under humid conditions. The planar device mounted on an alumina substrate with a Pt heater showed stable electromotive force (emf) responses to changes in the CO2 concentration (100-400 ppm) at 400 and 450°C in humid air without degradation. The sensor device also exhibited a good warming-up characteristic, i.e., the emf of the device quickly reached a steady and constant value when the sensor operation was restarted even after the sensor was exposed to humid air (86% relative humidity at 25°C) at room temperature for a long time. © 2008 The Electrochemical Society.
  • Organic gas sensor using BiCuVOx solid electrolyte, Tetsuya Kida, Takuya Minami, Masayoshi Yuasa, Kengo Shimanoe, Noboru Yamazoe, Electrochemistry Communications, 10, 311, 314,   2008年02月01日, 10.1016/j.elecom.2007.12.013, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=38649111963&origin=inward
    概要:A potentiometric organic gas sensor-based on BiCuVOx (Bi2Cu0.1V0.9O5.35) solid electrolyte was investigated. Electromotive force (EMF) of the sensor device, in which a BiCuVOx sintered disk is fitted with composite electrodes of BiCuVOx/La0.6Sr0.4Co0.78Ni0.02Fe0.2O3, was measured in the presence of various organic gases at 350-500 °C. The device responded to volatile organic compounds (VOC) of formaldehyde, toluene, and ethanol, but showed little sensitivities to methane, propane, propene, CO, and H2. The EMF of the sensor was linear to the logarithm of organic gas concentrations, suggesting that the generation of EMF is explained on the basis of the mixed potential theory. The observed good sensitivity toward VOC derives from the good oxide ion conductivity of BiCuVOx and proper electro-catalytic activity of the perovskite oxide electrode even at lower temperature. © 2008 Elsevier B.V. All rights reserved.
  • Nasicon-based planar-type cO2 sensor attached with solid reference electrode stable under high humid conditions, T. Kida, S. Kishi, M. Yuasa, K. Shimanoe, N. Yamazoe, TRANSDUCERS and EUROSENSORS '07 - 4th International Conference on Solid-State Sensors, Actuators and Microsystems, 975, 978,   2007年12月01日, 10.1109/SENSOR.2007.4300295, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=50049120495&origin=inward
    概要:In order to improve the stability of a NASICON (Na3Zr 2Si2PO12; Na+ conductor)-based potentiometric CO2 sensor under humid conditions, a new solid-reference electrode of the BiCuVOx (Bi2Cu0.1V 0.9O5.35)/perovskite-type oxide (La0.6Sr 0.4Co0.02Ni0.02Fe0.2O3) composite was investigated. The fabricated electrochemical cell (CO 2+O2, Au/ Li2CO3-BaCO3/ NASICON/ BiCuVOx-La0.6Sr0.4Co0.78Ni 0.02Fe0.2O3, O2) responded well to changes in CO2 concentration (100-400 ppm) at 400-450 °C under high humid conditions (86 %RH) without degradation. The sensor device also exhibited a good warming-up characteristic, i.e., the electromotive force of the device quickly reached a steady and constant value when the sensor operation is re-started even after the sensor was exposed to high humid air at room temperature. ©2007 IEEE.
  • A stable solid-reference electrode of BiCuVOx/perovskite-oxide for potentiometric solid electrolyte CO2 sensor, Shotaro Kishi, Masayoshi Yuasa, Tetsuya Kida, Vilho Eelis Lantto, Kengo Shimanoe, Noboru Yamazoe, Nippon Seramikkusu Kyokai Gakujutsu Ronbunshi/Journal of the Ceramic Society of Japan, 115, 706, 711,   2007年11月01日, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=44849102394&origin=inward
    概要:A laminated solid-reference electrode of BiCuVOx (Bi 2Cu0.1V0.9O5.35)/Jperovskite-oxide (La0.6Sr0.4Co0.78Ni0.02 Fe 0.2O3) was developed for a NASICON (Na3Zr 2Si2PO12; Na+ conductor)-based potentiometric CO2 sensor. The fabricated electrochemical cell expressed as, CO2, O2/Au (sensing electrode)JLi 2CO3-BaCO3 (auxiliary phase)JNASICON/ BiCuVOx/BiCuVOx-perovskite-oxide (reference electrode) /O2, responded well to changes in CO2 concentration (100-400 ppm) at 450°C under high humid conditions (88%RH). The potential of the developed reference electrode was stable and exhibited little interference by water vapor. Furthermore, the reference electrode potential did not response to CO2 even after the BiCuVOx layer was contaminated with carbonate, indicating a good stability of BiCuVOx against CO 2. The sensor device attached with the laminated solid-reference electrode showed a good warming-up characteristic, i.e., the electromotive force (EMF) of the device reached a steady and constant value when the sensor operation is re-started even after the sensor was exposed to humid air containing CO2 at room temperature.
  • Preparation of carbon-supported nano-sized LaMnO3 using reverse micelle method for energy-saving oxygen reduction cathode, Masayoshi Yuasa, Kengo Shimanoe, Yasutake Teraoka, Noboru Yamazoe, Catalysis Today, 126, 313, 319,   2007年08月30日, 10.1016/j.cattod.2007.06.006, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=34547690959&origin=inward
    概要:Two ways of reverse micelle (RM) method were investigated to prepare carbon-supported nano-sized LaMnO3 with high oxygen reduction activity. Hydrolysis precipitation in reverse micelle (HP-RM) method could give nano-sized particles of LaMnO3 easily because the particles size decreased with decreasing Rw (=[H2O]/[surfactant]) value as well as nitrate concentration. The electrode prepared by the resulting particles showed high oxygen reduction activity as compared with that prepared by mechanical mixing-method. Furthermore, it was found that new RM method (ROP-RM) using KMnO4 as an oxidizer gave higher oxygen reduction activity than the HP-RM method, although particle size of LaMnO3 obtained by the ROP-RM method was almost same as that by RM-HP method. © 2007.
  • New approach towards preparation of efficient gas diffusion-type oxygen reduction electrode, Jerzy P. Lukaszewicz, Shin Imaizumi, Masayoshi Yuasa, Kengo Shimanoe, Noboru Yamazoe, Journal of Materials Science, 41, 6215, 6220,   2006年10月01日, 10.1007/s10853-006-0723-2, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=34250373009&origin=inward
    概要:A novel method by combining NAC-FAS (NAnometer-sized Crystal Formation in Alcoholic Solutions) method and mechanical milling treatment was successfully applied for dispersing perovskite type oxide LaMnO3 finely on carbon support. Microscopic observation revealed that nano-sized oxide particles were dispersed fairly well in the carbon support. The gas diffusion-type electrode prepared by means of reducing number and quantity of chemicals exhibited more excellent oxygen reduction activity than the electrodes containing LaMnO 3 prepared by RHP (Reverse Homogeneous Precipitation) method. It allowed current density as high as 300 mA cm-2 at -80 mV (vs. Hg/HgO) in 8 M KOH at 60 °C under air flow. © Springer Science+Business Media, Inc. 2006.
  • SnO2クラスター分散水溶液を用いた高感度薄膜型ガスセンサの検討, 吉田 宏平, 湯浅 雅賀, 島ノ江 憲剛, Proceedings of the Chemical Sensor Symposium, 41, 4, 6,   2006年04月, http://ci.nii.ac.jp/naid/40007380815
  • 逆ミセル法によるSnO2ナノ粒子上へのPd担持の検討, 眞崎 貴則, 湯浅 雅賀, 島ノ江 憲剛, Proceedings of the Chemical Sensor Symposium, 42, 145, 147,   2006年09月, http://ci.nii.ac.jp/naid/40015136645
  • 高速ガス置換による半導体ガスセンサの応答特性解析, 黒岩 徹, 湯浅 雅賀, 島ノ江 憲剛, Proceedings of the Chemical Sensor Symposium, 42, 148, 150,   2006年09月, http://ci.nii.ac.jp/naid/40015136646
  • BaTiO3系PTCサーミスターを用いた可燃性ガスセンサの検討, 永野 崇仁, 湯浅 雅賀, 島ノ江 憲剛, Proceedings of the Chemical Sensor Symposium, 42, 151, 153,   2006年09月, http://ci.nii.ac.jp/naid/40015136647
  • FET型NOxセンサの検知電極の検討, 井上 浩文, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 43, 94, 96,   2007年03月, http://ci.nii.ac.jp/naid/40015522439
  • BiCuVOx固体電解質を用いたVOCsセンサの検討, 南 卓也, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 43, 130, 132,   2007年03月, http://ci.nii.ac.jp/naid/40015522451
  • 固体電解質CO2ガスセンサにおける固体参照極/NASICON固体電解質界面の構造解析, 岸 章太郎, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 43, 136, 138,   2007年03月, http://ci.nii.ac.jp/naid/40015522453
  • 逆ミセル法によりPdOを微細担持したSnO2半導体ガスセンサのガス検知特性, 湯浅 雅賀, 眞崎 貴則, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 44, 4, 6,   2007年09月, http://ci.nii.ac.jp/naid/40015668749
  • BiCuVO_x/ペロブスカイト酸化物-固体参照電極を取り付けた固体電解質二酸化炭素センサ(秋季シンポジウム若手研究者論文), 岸 章太郎, 湯浅 雅賀, 木田 徹也, LANTTO Vilho Eelis, 島ノ江 憲剛, 山添 昇, 日本セラミックス協会学術論文誌 : Nippon Seramikkusu Kyokai gakujutsu ronbunshi = Journal of the Ceramic Society of Japan, 115, 1347, 706, 711,   2007年11月01日, http://ci.nii.ac.jp/naid/110006438672
    概要:A laminated solid-reference electrode of BiCuVO_x (Bi_2Cu_<0.1>V_<0.9>O_<5.35>)/perovskite-oxide (La_<0.6>Sr_<0.4>Co_<0.78>Ni_<0.02> Fe_<0.2>O_3) was developed for a NASICON (Na_3Zr_2Si_2PO_<12> ; Na^+ conductor)-based potentiometric CO_2 sensor. The fabricated electrochemical cell expressed as, CO_2, O_2/Au (sensing electrode)/Li_2CO_3-BaCO_3 (auxiliary phase)/NASICON/BiCuVO_x/BiCuVO_x-perovskite-oxide (reference electrode)/O_2, responded well to changes in CO_2 concentration (100-400ppm) at 450℃ under high humid conditions (88%RH). The potential of the developed reference electrode was stable and exhibited little interference by water vapor. Furthermore, the reference electrode potential did not response to CO_2 even after the BiCuVO_x layer was contaminated with carbonate, indicating a good stability of BiCuVO_x against CO_2. The sensor device attached with the laminated solid-reference electrode showed a good warming-up characteristic, i.e., the electromotive force (EMF) of the device reached a steady and constant value when the sensor operation is re-started even after the sensor was exposed to humid air containing CO_2 at room temperature.
  • TiO2ガスセンサの微細構造制御とガス検知特性, 徐 敏鉉, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 45, 22, 24,   2008年03月, http://ci.nii.ac.jp/naid/40015986431
  • BiCuVOx固体電解質ガスセンサの電極構造の検討, 南 卓也, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 45, 31, 33,   2008年03月, http://ci.nii.ac.jp/naid/40015986434
  • ラメラ状WO3を用いたNO2センサの微細構造とガス応答特性, 西山 綾, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 46, 46, 48,   2008年09月, http://ci.nii.ac.jp/naid/40016279333
  • SnO2ナノ粒子へのFe[3+]ドーピングとセンサ特性, 末松 昴一, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 46, 52, 54,   2008年09月, http://ci.nii.ac.jp/naid/40016279335
  • Oxygen Permeation of a Dense/Porous Asymmetric Membrane Using La_<0.6>Ca_<0.4>CoO_<3-δ>-BaFe_<0.975>Zr_<0.025>O_<3-δ> System, WATANABE Ken, YUASA Masayoshi, KIDA Tetsuya, SHIMANOE Kengo, TERAOKA Yasutake, YAMAZOE Noboru, Chemistry letters, 38, 1, 94, 95,   2009年01月05日, http://ci.nii.ac.jp/naid/10023990739
  • SnO2ガスセンサにおける結晶子径及びドナー密度の影響, 末松 昴一, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 47, 34, 36,   2009年03月, http://ci.nii.ac.jp/naid/40016615123
  • TiO2ナノチューブを用いた有機ガス検知の検討, 徐 敏鉉, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 47, 40, 42,   2009年03月, http://ci.nii.ac.jp/naid/40016615125
  • FET型NO2センサにおけるNaNO2系検知補助相への貴金属添加量の影響, 井上 浩文, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 47, 58, 60,   2009年03月, http://ci.nii.ac.jp/naid/40016615131
  • 半導体ガスセンサにおける粒子サイズと感応膜利用効率の関係, 藤山 修平, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 48, 85, 87,   2009年09月, http://ci.nii.ac.jp/naid/40016854566
  • 炭酸塩を補助相とするMetal-Insulator-SiC構造CO2センサの検討, 井上 浩文, Andersson Mike, 湯浅 雅賀, Proceedings of the Chemical Sensor Symposium, 49, 46, 48,   2010年03月, http://ci.nii.ac.jp/naid/40017082297
  • BaTiO3系サーミスタを用いた水素センサの高感度化, 立花 直樹, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 49, 58, 60,   2010年03月, http://ci.nii.ac.jp/naid/40017082301
  • 分極曲線・サイクリックボルタンメトリー(15)ガス拡散電極 空気電池用正極, 湯浅 雅賀, 島ノ江 憲剛, 電気化学および工業物理化学 : denki kagaku, 78, 7, 629, 632,   2010年07月05日, http://ci.nii.ac.jp/naid/10026485485
  • 半導体ガスセンサにおける粒子径効果と利用効率の相関, 島ノ江 憲剛, 藤山 修平, 湯浅 雅賀, Proceedings of the Chemical Sensor Symposium, 50, 76, 78,   2010年09月, http://ci.nii.ac.jp/naid/40017357986
  • Au担持TiO2ナノチューブセンサのVOCガスに対する応答特性, 徐 敏鉉, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 50, 94, 96,   2010年09月, http://ci.nii.ac.jp/naid/40017357992
  • 逆ミセル法によるランタンーマンガン系ペロブスカイト型酸化物の合成と酸素還元電極への応用, 湯浅 雅賀, 島ノ江 憲剛, セラミックス, 46, 1, 17, 21,   2011年01月01日, http://ci.nii.ac.jp/naid/10028235712
  • 固体電解質NASICONに複合酸化物電極を接合した有機ガスセンサの検討, 森永 直樹, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 51, 103, 105,   2011年03月, http://ci.nii.ac.jp/naid/40018913103
  • SnO2半導体の電気的特性に及ぼす水蒸気の効果, 末松 昂一, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 51, 148, 150,   2011年03月, http://ci.nii.ac.jp/naid/40018913118
  • SnO2半導体表面への酸素吸着特性における水蒸気吸着の影響, 末松 昴一, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 52, 13, 15,   2011年09月, http://ci.nii.ac.jp/naid/40019025276
  • 熱安定性に優れた酸化スズナノ粒子の合成とガス検知特性, 湯浅 雅賀, 山田 清美, 渡邉 賢, Proceedings of the Chemical Sensor Symposium, 52, 16, 18,   2011年09月, http://ci.nii.ac.jp/naid/40019025277
  • SnO₂ナノ粒子ガスセンサにおける水素応答メカニズムの検討, 末松 昂一, 湯浅 雅賀, 木田 徹也, Proceedings of the Chemical Sensor Symposium, 53, 0, 115, 117,   2012年03月, http://ci.nii.ac.jp/naid/40019318798
  • 水熱処理法によるパラジウム担持酸化スズクラスターの調製とそのガス検知特性, 進 由佳, 末松 昂一, 湯浅 雅賀, Proceedings of the Chemical Sensor Symposium, 53, 0, 118, 120,   2012年03月, http://ci.nii.ac.jp/naid/40019318805
  • Reverse micelle-based preparation of carbon-supported La 1-xSrxMn1-yFeyO3+δ for oxygen reduction electrode, M. Yuasa, G. Sakai, K. Shimanoe, Y. Teraoka, N. Yamazoe, Journal of the Electrochemical Society, 151,   2004年11月26日, 10.1149/1.1789156, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=8644242324&origin=inward
    概要:La1-xSrxMn0.8Fe0.2O 3+δ (x = 0-0.4) and La0.8Sr0.2Mn 1-yFeyO3+δ (y = 0-0.8) supported on carbon were successfully prepared by a reverse micelle method. Aqueous solutions dissolving nitrates of constituent metals of the intended oxides and tetramethylammonium hydroxide (precipitant) were separately transformed into reverse micelle dispersions by using poly(oxyethylene)5-lauryl ether (surfactant) and cyclohexane (oil). These dispersions were mixed together to derive a reverse micelle dispersion containing mixed hydroxides as precursors of the oxides, into which carbon powder suspended in cyclohexane was put under agitation. The suspension was destabilized with ethanol, and the resulting precipitate (carbon-supported precursors) was calcined in N2 atmosphere to prevent the carbon matrix from being combusted. Single-phase oxides supported on carbon were obtained by calcination at 700°C unless the oxides were free of Fe. Oxygen reduction activity of the gas-diffusion-type electrodes fabricated with thus prepared carbon-supported oxides increased sharply and decreased gradually with increasing x and y, respectively. Among the prepared oxides, the greatest activity, i.e., 500 mA/cm2 at -67 mV (vs. Hg/HgO electrode) in 9 M NaOH at 85°C under O2 flow, was achieved by the oxide with x = 0.4 and y = 0.2. Optimal loading on carbon as well as durability under oxygen reduction conditions were tested for selected oxides. 17 wt % La0.6Sr0.4Mn0.8Fe 0.2O3+δ loading electrode was compared with 27.7 wt % Pt-loading electrode in an oxygen reduction activity, and it was found that the former electrode was better than the Pt loading electrode. © 2004 the electrochemical society All rights reserved.
  • Exploration of reverse micelle synthesis of carbon-supported LaMnO 3, M. Yuasa, G. Sakai, K. Shimanoe, Y. Teraoka, N. Yamazoe, Journal of the Electrochemical Society, 151,   2004年10月18日, 10.1149/1.1782165, http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=4944261830&origin=inward
    概要:Reverse micelle (RM) based synthesis of carbon-supported perovskite type oxide (LaMnO3) was investigated. By using cyclohexane as oil phase, six kinds of nonionic surfactants were tested for the formation of the revere micelle dispersions containing aqueous solutions of mixed nitrates of La 3+ and Mn2+ (RM-N) and tetramethylammonium hydroxide (RM-A) at the water/surfactant molar ratio (Rw) of 3. RM-A was found to be more difficult to form compared with RM-N or the RM containing pure water. At a temperature range of 5-25°C, it was given only by the surfactants with hydrophilic-lipophilic balance (HLB) values of 10.0-10.9. Phase diagrams of oil-surfactant-alkaline solution (or pure water) were constructed at 5 and 15°C for the best two surfactants, i.e., poly-(oxyetylene) 6-nonylphenyl ether and poly-(oxyetylene)5-lauryl ether. Mixing RM-N and RM-A together gave the RM containing a mixed hydroxides-precursor (RM-P), which was further converted into carbon-supported LaMnO3 through a series of treatments including the addition of carbon powder and calcination in N2 atmosphere at 600°C. The size of RM-P as well as that of the LaMnO3 grains supported on carbon could be controlled well by selecting Rw. The carbon-supported LaMnO3 proved to be highly active for the electrochemical reduction of oxygen. © 2004 The Electrochemical Society. All rights reserved.

特許

  • リチウム空気二次電池, 林 政彦, 蓑輪 浩伸, 林 克也, 小林 隆一, 島ノ江 憲剛, 木田 徹也, 湯浅 雅賀, 特願2013-144975, 特開2015-018679
  • 空気電池用ガス拡散電極およびその作製方法ならびに空気電池, 松元 隆志, 新井 健太郎, 斉藤 憲明, 木野 貴允, 岩本 淳, 島ノ江 憲剛, 湯浅 雅賀, 特願2012-191962, 特開2014-049304
  • SnO2ガスセンサの製造方法と、貴金属ナノ粒子を担持したSnO2の製造方法, 島ノ江 憲剛, 木田 徹也, 湯浅 雅賀, 特願2008-194402, 特開2010-032343
  • 酸素分離膜, 島ノ江 憲剛, 寺岡 靖剛, 山添 ▲昇▼, 木田 徹也, 湯浅 雅賀, 高内 大輔, 渡邉 賢, 特願2007-146704, 特開2008-296162
  • BiMeVOx系VOCsセンサ, 島ノ江 憲剛, 山添 昇, 木田 徹也, 湯浅 雅賀, 南 卓也, 特願2007-078736, 特開2008-241299, 特許第4859129号
  • SnO2ガスセンサの製造方法, 島ノ江 憲剛, 山添 昇, 湯浅 雅賀, 特願2006-244356, 特開2008-064674, 特許第4794398号

受賞

  •   2011年11月, Outstanding paper of International Conference on Advanced Electromaterials 2011

競争的資金

  • 文部科学省, 科学研究費補助金(基盤研究(C)), 高性能な金属空気二次電池用空気極のための触媒担持導電性酸化物の精密合成, 湯浅 雅賀
  • 徳山科学技術振興財団, 平成25年度 徳山科学技術振興財団研究助成, 導電性酸化チタンナノ粒子の合成と金属空気二次電池用空気極への応用, 湯浅雅賀
  • 大倉和親記念財団, 平成24年度 大倉和親記念財団 学術研究助成, 異種酸化物半導体ナノ粒子の接合で構築した室温作動型半導体ガスセンサの開発, 湯浅雅賀
  • 文部科学省, 科学研究費補助金(若手研究(B)), 高出力な金属空気電池のための空気極のナノ材料設計, 湯浅 雅賀, La-Mn系ペロブスカイト型酸化物を電極触媒とした金属空気電池用空気極の酸素還元電位を向上するために、酸化物組成およびPtとLaMnO3の共担持の効果について検討を行った。LaMnO3にCa,Feを置換し、酸素還元活性を調べた結果、酸素還元活性はMnサイトの酸化数に依存する傾向にあることがわかった。また、ペロブスカイト型酸化物中のAサイト欠陥が酸素還元活性の向上に寄与している可能性が示唆された。LaMnO3ナノ粒子と微量のPtとをカーボン担体に共担持した酸素還元触媒を合成し、その特性を調べた結果、Ptが空気極の浸漬電位の向上に、LaMnO3が過電圧の削減に有効に作用することが明らかとなった。
  • 科学技術振興機構, 研究成果最適展開支援事業A-STEPフィージビリティスタディ【FS】ステージ探索タイプ, 金属空気電池の二次電池化に向けた導電性酸化物空気極の開発, 湯浅雅賀
  • 日本板硝子材料工学助成会, 平成20年度 日本板硝子材料工学助成金, Pd/SnO2ナノコンポジットの液相合成と半導体ガスセンサへの応用, 湯浅雅賀
  • 文部科学省, 科学研究費補助金(若手研究(B)), 金属空気電池の二次電池化のための新規空気電極の創製, 湯浅 雅賀, 金属空気電池は最も理論エネルギー密度の高い電池であり、次世代のエネルギーデバイスとして注目されている。しかし現在の空気電池は、空気中の酸素を取り込む空気極が充電反応の際に腐食劣化するため、二次電池として動作しない。そこで本研究では、腐食劣化を起こさず、電極反応に高活性なLaNiO_3ナノ粒子を従来の空気極材料の代替として用いるための研究を行った。その結果、LaNiO_3が従来の材料の代替となりうることを見出し、さらに、LaMnO_3とLaNiO_3を組み合わせることで充放電可能な空気極となることが明らかとなった。

その他

  •   2016年04月, 高性能金属空気二次電池の実現に向けたグラフェン複合材料の開発, 近畿大学学内研究助成金 奨励研究助成金 SR17 研究内容:金属空気電池用空気極のカーボン代替材料として、触媒担持グラフェンの使用を検討した。