Performance comparison of low-temperature direct alcohol fuel cells with different anode catalysts

被引:194
作者
Zhou, WJ
Zhou, B
Li, WZ
Zhou, ZH
Song, SQ
Sun, GQ
Xin, Q
Douvartzides, S
Goula, A
Tsiakaras, P
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Direct Alcohol Fuel Cells Lab, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Natl Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Univ Thessaly, Dept Mech & Ind Engn, Volos 38334, Volos, Greece
[4] Headwaters Nanokinetix, Lawrenceville, NJ 08648 USA
基金
中国国家自然科学基金;
关键词
direct methanol fuel cell; direct ethanol fuel cell; PtRu anode; PtSn anode;
D O I
10.1016/j.jpowsour.2003.08.009
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
Low-temperature polymer electrolyte membrane fuel cells directly fed by methanol and ethanol were investigated employing carbon supported Pt, PtSn and PtRu as anode catalysts, respectively. Employing Pt/C as anode catalyst, both direct methanol fuel cell (DMFC) and direct ethanol fuel cell (DEFC) showed poor performances even in presence of high Pt loading on anode. It was found that the addition of Ru or Sn to the Pt dramatically enhances the electro-oxidation of both methanol and ethanol. It was also found that the single cell adopting PtRu/C as anode shows better DMFC performance, while PtSn/C catalyst shows better DEFC performance. The single fuel cell using PtSn/C as anode catalyst at 90degreesC shows similar power densities whenever fueled by methanol or ethanol. The cyclic voltammetry (CV) and single fuel cell tests indicated that PtRu is more suitable for DMFC while PtSn is more suitable for DEFC. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:16 / 22
页数:7
相关论文
共 47 条
[1]   Investigation of PEMFC operation above 100°C employing perfluorosulfonic acid silicon oxide composite membranes [J].
Adjemian, KT ;
Srinivasan, S ;
Benziger, J ;
Bocarsly, AB .
JOURNAL OF POWER SOURCES, 2002, 109 (02) :356-364
[2]   Formation of carbon-supported PtM alloys for low temperature fuel cells: a review [J].
Antolini, E .
MATERIALS CHEMISTRY AND PHYSICS, 2003, 78 (03) :563-573
[3]  
ANTONUCCI V, 2002, FUELS CELLS B, V7, P6
[4]   STUDY OF METHANOL ELECTROOXIDATION ON RH-SN OXIDE, PT-SN OXIDE, AND IR-SN OXIDE IN COMPARISON WITH THAT ON THE PT METALS [J].
ARAMATA, A ;
TOYOSHIMA, I ;
ENYO, M .
ELECTROCHIMICA ACTA, 1992, 37 (08) :1317-1320
[5]  
Aricò AS, 2001, FUEL CELLS, V1, P133
[6]  
Aricò AS, 1998, ELECTROCHEM SOLID ST, V1, P66, DOI 10.1149/1.1390638
[7]   Effect of carbon-supported and unsupported Pt–Ru anodes on the performance of solid-polymer-electrolyte direct methanol fuel cells [J].
A.S. Aricò ;
A.K. Shukla ;
K.M. El-Khatib ;
P. Cretì ;
V. Antonucci .
Journal of Applied Electrochemistry, 1999, 29 (6) :673-678
[8]   Formic acid oxidation on ultrathin Pd films on Au(hkl) and Pt(hkl) electrodes [J].
Baldauf, M ;
Kolb, DM .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (27) :11375-11381
[9]   EFFECT OF BI AND SN ADATOMS ON FORMIC-ACID AND METHANOL OXIDATION AT WELL DEFINED PLATINUM SURFACES [J].
CAMPBELL, SA ;
PARSONS, R .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1992, 88 (06) :833-841
[10]   METAL CRYSTALLINITY EFFECTS IN ELECTROCATALYSIS AS PROBED BY REAL-TIME FTIR SPECTROSCOPY - ELECTROOXIDATION OF FORMIC-ACID, METHANOL, AND ETHANOL ON ORDERED LOW-INDEX PLATINUM SURFACES [J].
CHANG, SC ;
LEUNG, LWH ;
WEAVER, MJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (15) :6013-6021