Particle-Size- and Ru-Core-Induced Surface Electronic States of Ru-Core/Pt-Shell Electrocatalyst Nanoparticles

被引:28
作者
Goto, Shuji [1 ,2 ]
Hosoi, Shizuka [1 ]
Arai, Ryoji [1 ]
Tanaka, Shinji [1 ]
Umeda, Minoru [3 ]
Yoshimoto, Mamoru [2 ]
Kudo, Yoshihiro [1 ]
机构
[1] Sony Corp, Adv Mat Labs, Atsugi, Kanagawa 2430014, Japan
[2] Tokyo Inst Technol, Dept Innovat & Engn Mat, Midori Ku, Yokohama, Kanagawa 2268502, Japan
[3] Nagaoka Univ Technol, Dept Mat Sci & Technol, Fac Engn, Nagaoka, Niigata 9402188, Japan
关键词
OXYGEN REDUCTION REACTION; PLATINUM-MONOLAYER ELECTROCATALYSTS; METHANOL FUEL-CELLS; CATALYTIC-ACTIVITY; CARBON NANOTUBES; PD; ELECTROOXIDATION; ADSORPTION; CLUSTERS; SPECTROSCOPY;
D O I
10.1021/jp411871y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The unique electrocatalytic properties of core/shell-structured bimetallic nanoparticles (NPs) are generally attributed to core-induced electronic effects on surface atoms. For small core/shell NPs, however, size-dependent electronic modifications can be non-negligible. Here, using synchrotron-based photoelectron spectroscopy, we identified both size- and core-induced modifications in the surface electronic states of core/shell NPs with approximately monolayer-thick Pt shells completely covering Ru cores. The embedded Ru cores were found to induce a downward shift in energy of the d states of the surface Pt atoms. However, with a decrease in core size from 1.9 to 1.3 nm, these Ru-core-induced, low-lying d states increased in energy and decreased in intensity. Extended X-ray absorption fine structure measurements indicated that this size-induced electronic modification can be associated with a decrease in the number of Pt-Ru bonds per surface Pt atom. The observed size- and core-induced electronic modifications were confirmed to affect the electrochemical desorption of CO from the core/shell NPs. Our findings indicate that both size- and core-induced electronic effects must be considered in the rational design of real-world core/shell electrocatalyst NPs.
引用
收藏
页码:2634 / 2640
页数:7
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