A strategy for easy synthesis of carbon supported Co@Pt core-shell configuration as highly active catalyst for oxygen reduction reaction

被引:35
|
作者
Li, Zesheng [1 ,2 ]
He, Chunyong [1 ,2 ]
Cai, Mei [3 ]
Kang, Shuai [1 ,2 ]
Shen, Pei Kang [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Phys & Engn, State Key Lab Optoelect Mat & Technol, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Sch Phys & Engn, Guangdong Prov Key Lab Low Carbon Chem & Energy C, Guangzhou 510275, Guangdong, Peoples R China
[3] Gen Motors Res & Dev Ctr, Warren, MI 48090 USA
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Co@Pt core-shell nanostructures; Branched morphologies; Supported electrocatalyst; Oxygen reduction reaction; Fuel cells; ELECTROCATALYTIC ACTIVITY; BIMETALLIC NANODENDRITES; NANOPARTICLES; OXIDATION;
D O I
10.1016/j.ijhydene.2012.07.100
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
An oxygen-mediated galvanic battery reaction strategy has been developed to one-step synthesize carbon-supported Co@Pt core-shell nanostructures. Relying on this strategy, a structural evolution of 3-D Pt-on-Co bimetallic nanodendrites into Co@Pt core-shell configuration is readily achieved in our study. These well-supported and low-Pt-content nanostructures show superior electrocatalytic activities to oxygen reduction reaction. Especially, the supported Co@Pt core-shell electrocatalyst for oxygen reduction reaction shows a high activity with the maximal Pt-mass activity of 465 mA mg(-1) Pt at 0.9 V (vs. RHE). The present investigation clearly demonstrates that the design and synthesis of the core-shell nanostructures is a viable route for building Pt-based electrocatalysts with optimized utilization efficiency and higher cost performance. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:14152 / 14160
页数:9
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