Direct ethanol PEM fuel cells: The case of platinum based anodes

被引:210
作者
Song, SQ
Zhou, WJ
Zhou, ZH
Jiang, LH
Sun, GQ
Xin, Q
Leontidis, V
Kontou, S
Tsiakaras, P
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Direct Alcohol Fuel Cell Lab, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Univ Thessaly, Sch Engn, Dept Mech Engn, Thessaly 38334, Greece
基金
中国国家自然科学基金;
关键词
direct ethanol fuel cells; PtSn/C; PtRu/C; ethanol electrooxidation;
D O I
10.1016/j.ijhydene.2004.11.006
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
PtSn/C catalysts were prepared by the direct decoration of Pt/C with Sn through a modified poly process. XRD results showed there existed obvious SnO2 in this catalyst, different from the PtSn/C prepared by co-precipitation, Sn presenting in different valence. The techniques of cyclic voltammetry, anode polarization curve and single direct ethanol fuel cell (DEFC) tests were used to evaluate and compare the electrocatalytic activities to ethanol oxidation over PtSn/C prepared by different preparation procedure and over the commercial PtRu/C catalyst. The experimental results showed that PtSn/C presents higher electrocatalytic activity than PtRu/C. The results also showed that, compared to the PtSn/C prepared by co-precipitation, PtSn/C in this investigation exhibits a similar initial activity but a lower activity along with the current density increment, probably due to its poor electronic conductivity and part coverage of platinum active sites resulting from SnO2. It was found from the GC analysis results that PtSn/C can oxidize ethanol molecules to a deeper extent than PtRu/C, leading to both a higher fuel utilization coefficient and a higher fuel cell efficiency. (c) 2005 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:995 / 1001
页数:7
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