A Highly Stable Anode, Carbon-Free, Catalyst Support Based on Tungsten Trioxide Nanoclusters for Proton-Exchange Membrane Fuel Cells

被引:33
作者
Dou, Meiling [1 ,2 ]
Hou, Ming [1 ]
Zhang, Huabing [1 ,2 ]
Li, Guangfu [1 ,2 ]
Lu, Wangting [1 ,2 ]
Wei, Zidong [3 ]
Shao, Zhigang [1 ]
Yi, Baolian [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Lab Fuel Cells, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] Chongqing Univ, Coll Chem & Chem Engn, State Key Lab Power Transmiss Equipment & Syst Se, Chongqing 400044, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
fuel cells; heterogeneous catalysis; Pt; tungsten; WO3; THIN-FILMS; METHANOL OXIDATION; ELECTROCHROMIC PROPERTIES; CO-TOLERANCE; OXIDE; ELECTROCATALYST; STARVATION; PLATINUM; DURABILITY; REVERSAL;
D O I
10.1002/cssc.201100706
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Durability is an important issue in proton-exchange membrane fuel cells (PEMFCs). One of the major challenges lies in the degradation caused by the oxidation of the carbon support under high anode potentials (under fuel starvation conditions). Herein, we report highly stable, carbon-free, WO3 nanoclusters as catalyst supports. The WO3 nanoclusters are synthesized through a hard template method and characterized by means of electron microscopy and electrochemical analysis. The electrochemical studies show that the WO3 nanoclusters have excellent electrochemical stability under a high potential (1.6 V for 10 h) compared to Vulcan XC-72. Pt nanoparticles supported on these nanoclusters exhibit high and stable electrocatalytic activity for the oxidation of hydrogen. The catalyst shows negligible loss in electrochemically active surface area (ECA) after an accelerated durability test, whereas the ECA of the Pt nanoparticles immobilized on conventional carbon decreases significantly after the same oxidation condition. Therefore, Pt/WO3 could be considered as a promising alternative anode catalyst for PEMFCs.
引用
收藏
页码:945 / 951
页数:7
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