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Carbon-supported Pd-Co bimetallic nanoparticles as electrocatalysts for the oxygen reduction reaction
被引:206
作者:
Wang, Wenming
Zheng, Dan
Du, Chong
Zou, Zhiqing
Zhang, Xigui
Xia, Baojia
Yang, Hui
[1
]
Akins, Daniel L.
机构:
[1] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, Energy Sci & Technol Lab, Shanghai 200050, Peoples R China
[2] Grad Univ, Chinese Acad Sci, Beijing 100039, Peoples R China
[3] CUNY City Coll, Dept Chem, Ctr Anal Struct & Interfaces, New York, NY 10031 USA
基金:
中国国家自然科学基金;
美国国家科学基金会;
关键词:
Pd-Co nanoparticle;
oxygen reduction reaction;
electrocatalysis;
methanol tolerance;
D O I:
10.1016/j.jpowsour.2007.02.013
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:
Carbon-supported Pd-Co bimetallic nanoparticle electrocatalysts of different Pd/Co atomic ratios were prepared by a modified polyol reduction. Electrocatalytic activities of the catalysts for the oxygen reduction reaction (ORR) have been investigated based on the porous rotating disk and disk-ring electrode techniques. As-prepared Pd-Co bimetallic nanoparticles evidence a single-phase fec disordered structure, and the mean particle size is found to decrease with increase in Co content. A typical TEM image of the Pd2Co/C catalyst, heat-treated at 500 degrees C, reveals a mean particle diameter is ca. 8.3 nm with a relatively narrow size distribution. For synthesized Pd-Co catalysts, the highest catalytic activity for the ORR, when supported on carbon (i.e., Pd-Co/C) was found for a Pd:Co atomic ratio of 2:1 and heat treatment at ca. 500 degrees C, corresponding to a Pd-Pd mean interatomic distance of ca. 0.273 nm. Kinetic analysis based on the rotating disk and disk-ring electrode measurements reveals that the ORR on Pd-Co/C catalysts undergoes a four-electron process in forming water Because the Pd-Co/C catalyst is inactive for the adsorption and oxidation of methanol, it may function as a methanol-tolerant ORR catalyst in a direct methanol fuel cell. (c) 2007 Elsevier B.V. All rights reserved.
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页码:243 / 249
页数:7
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