Highly stable PtRuTiOx/C anode electrocatalyst for direct methanol fuel cells

被引:70
|
作者
Tian, Juan
Sun, Gongquan [1 ]
Jiang, Luhua
Yan, Shiyou
Mao, Qing
Xin, Qin
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Direct Alcohol Fuel Cell Lab, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
direct methanol fuel cell; PtRu electrocatalyst; titanium oxide; thermal treatment; durability;
D O I
10.1016/j.elecom.2006.10.034
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In the present investigation, PtRuTiOx/C electrocatalyst was prepared by a modified polyol synthesis method and the as-prepared electrocatalyst was treated under the reductive atmosphere (30 vol% H-2 in Ar) at 500 degrees C for 2 h (denoted as PtRuTiOx/C-500) to enhance the interaction between the metal particles and the support. For comparison, the commercial PtRu/C electrocatalyst was also treated by the same procedure as PtRuTiOx/C (denoted as PtRu/C-500). Transmission electron microscopy results indicated that PtRuTiOx/C electrocatalyst exhibited not only a uniform dispersion and narrow size distribution with a smaller particle size, but also excellent stability during the thermal treatment. In contrast, the commercial PtRu/C electrocatalyst is not stable during the thermal treatment and the metal particles greatly agglomerated. The results of CO-stripping voltammetry, single direct methanol fuel cell tests and life-time test jointly showed that PtRuTiOx/C-500 had better durability than commercial PtRu/C while keeping a desirable activity toward methanol electro-oxidation, which may be attributed to the addition of titanium oxide that improved the interaction between noble metal particles and the support. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:563 / 568
页数:6
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