Takuya Masuda 교수

In situ electrochemical X-ray absorption fine structure (XAFS) measurements were performed at the Pt L3 and Ce L3 edges of the Pt–CeOx/C catalyst, which was prepared by a combined process of precipitation and coimpregnation methods, as well as at the Pt L3 edge of the conventional Pt/C catalyst in oxygen-saturated H2SO4 solution to clarify the role of CeOx in the reduction of the overpotential for the oxygen reduction reaction (ORR) at the Pt–CeOx nanocomposite compared with the conventional Pt/

In situ electrochemical X-ray photoelectron spectroscopy (XPS) apparatus, which allows XPS at solid/liquid interfaces under potential control, was constructed utilizing a microcell with an ultra-thin Si membrane, which separates vacuum and a solution. Hard X-rays from a synchrotron source penetrate into the Si membrane surface exposed to the solution. Electrons emitted at the Si/solution interface can pass through the membrane and be analyzed by an analyzer placed in vacuum. Its operation was de

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTransition metal catalyzed asymmetric organic syntheses via polymer-attached optically active phosphine ligands. Synthesis of R amino acids by hydrogenation with a polymer catalyst containing optically active alcohol sitesT. Masuda and J. K. StilleCite this: J. Am. Chem. Soc. 1978, 100, 1, 268–272Publication Date (Print):January 1, 1978Publication History Published online1 May 2002Published inissue 1 January 1978https://doi.org/10.1021/ja00469a045RIGHT

Potential-dependent adsorption/desorption behavior of perfluorosulfonated ionomer (PFSI) on a platinum electrode was investigated by cyclic voltammetry, electrochemical quartz crystal microbalance (EQCM), and electrochemical atomic force microscope (EC-AFM) in a Nafion, that is, PFSI, dispersed aqueous solution without any other electrolyte. PFSI adsorbed on the platinum surface in the potential region between 0.1 and 0.8 V versus Ag/AgCl and desorbed from the surface at 1.1 V where place-exchan

<i>In situ</i> X-ray photoelectron spectroscopy is applied to electrochemical lithiation/delithiation processes of an amorphous Si electrode sputter-deposited on a Li_6.6La₃Zr_1.6Ta_0.4O₁₂ solid electrolyte. After the first lithiation, a broad Li peak appears at the Si surface, and peaks corresponding to bulk Si and Si suboxide significantly shift to lower binding energy. The appearance of the Li peak and shift of the Si peaks confirm the forma

Potential-dependent adsorption/desorption behavior of perfluorosulfonated ionomer (PFSI) on a gold electrode was investigated by cyclic voltammetry (CV), electrochemical quartz crystal microbalance (EQCM), and electrochemical atomic force microscopy (EC-AFM) in a Nafion (i.e., PFSI) dispersed aqueous solution without any other electrolyte. It was found that PFSI serves as an electrolyte and that electrochemical measurements can be performed in this solution without any significant IR drop. PFSI

Abstract Adsorption process and structure of perfluorosulfonated acid (PFSA) polymer on a highly oriented pyrolytic graphite (HOPG) surface were elucidated by an in situ tapping mode atomic force microscope (AFM). Micellar aggregates of PFSA polymers first randomly adsorbed on a bare HOPG surface, and then the adsorbed aggregates extended under the influence of atomic arrangement of HOPG surface, to form two-dimensionally ordered domains.

The structure of the perfluorosulfonated ionomer (PFSI)/Pt(111) interface in a membrane electrode assembly (MEA)-like configuration of a polymer electrolyte membrane (PEM) fuel cell, that is, a vacuum evaporated Pt layer/PEM(Nafion membrane)/PFSI(adhesion Nafion layer)/Pt(111) single crystal, and its bias-induced change were investigated by surface X-ray scattering measurement at an atomic level. Crystal truncation rod measurement shows that PFSI adsorbed on the Pt(111)-(1 × 1) surface without b