Core-shell structured SiC@C supported platinum electrocatalysts for direct methanol fuel cells

被引:34
|
作者
Zang, Jianbing [1 ]
Dong, Liang [1 ]
Jia, Yingdan [1 ]
Pan, Hong [1 ]
Gao, Zhenzhen [1 ]
Wang, Yanhui [1 ]
机构
[1] Yanshan Univ, Coll Mat Sci & Engn, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Peoples R China
基金
中国国家自然科学基金;
关键词
Nano-SiC; Graphitization; Support; Eletrocatalyst; Stability; OXYGEN-REDUCTION REACTION; CATALYST SUPPORT; RAMAN-SCATTERING; ACID-SOLUTIONS; SURFACE-AREA; THIN-FILMS; DURABILITY; ELECTRODES; ELECTROOXIDATION; NANOPARTICLES;
D O I
10.1016/j.apcatb.2013.06.031
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
Core-shell structured SiC@C with a nanoscale SiC core covered by a graphitic carbon shell was used as a novel support for Pt electrocatalyst in direct methanol fuel cells (DMFCs) to achieve high durability and catalytic performance. The SiC@C was prepared by graphitization of nano-SiC under a vacuum of 10(-3) Pa at 1500 degrees C. The epitaxial growth carbon layer had a high conductivity and an affinity for Pt catalyst metal, while SiC core retained its high stability. Pt electrocatalysts supported on SiC@C (Pt/SiC@C) were prepared using a microwave heating method. The electrochemical results showed that the Pt/SiC@C electrocatalyst had much higher catalytic activities for methanol electro-oxidation and oxygen reduction reactions than the Pt/SiC. More significantly, the Pt/SiC@C electrocatalyst showed a greater stability in comparison to the traditional Pt/C. The superior electrocatalytic performances of Pt/SiC@C were ascribed to a high dispersion of Pt nanoparticles on the SiC@C support and a high stability of the SiC@C support in acid solution. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:166 / 173
页数:8
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