Oxygen Reduction Kinetics on Pt Monolayer Shell Highly Affected by the Structure of Bimetallic AuNi Cores

被引:47
作者
Chen, Guangyu [1 ,2 ]
Kuttiyiel, Kurian A. [2 ]
Su, Dong [3 ]
Li, Meng [2 ]
Wang, Chiu-Hui [2 ]
Buceta, David [2 ]
Du, Chunyu [1 ]
Gao, Yunzhi [1 ]
Yin, Geping [1 ]
Sasaki, Kotaro [2 ]
Vukmirovic, Miomir B. [2 ]
Adzic, Radoslav R. [2 ]
机构
[1] Harbin Inst Technol, Sch Chem Engn & Technol, State Key Lab Urban Water Resource & Environm, Harbin 150001, Peoples R China
[2] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[3] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
基金
中国国家自然科学基金;
关键词
RAY-ABSORPTION SPECTROSCOPY; FUEL-CELL CATALYSTS; PLATINUM-MONOLAYER; NANOPARTICLE ELECTROCATALYSTS; ALLOY NANOPARTICLES; CHARGE REDISTRIBUTION; O-2; REDUCTION; CARBON; METAL; CO;
D O I
10.1021/acs.chemmater.6b00500
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
We describe pronounced effects of structural changes of the AuNi cores on the oxygen reduction reaction (ORR) activity of a Pt monolayer shell. The study of alloyed AuNi nanoparticles compared with AuNi core shell structured nanoparticles revealed configurations having different electronic and electrochemical properties. Controlled alloying of Au with Ni was essential to tune the electronic properties of Au interacting with the Pt monolayer shell to achieve suitable adsorption of 02 on Pt for expediting the ORR The alloyed AuNi nanoparticles made the Pt shell more catalytically active for the ORR than the core shell structured AuNi nanoparticles. The Pt monolayer supported on the alloyed AuNi nanoparticles showed the Pt mass and specific activities as high as 1.52 A mg(-1) and 1.18 mA cm(-2), respectively, with almost no loss over 5 000 cycles of stability test. This high ORR activity is ascribed to the role of nonspecific steric configuration of Ni atoms changing the electronic properties of the alloy that affect the oxygen and water interaction with the Pt shell and facilitate increased ORR kinetics.
引用
收藏
页码:5274 / 5281
页数:8
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