Improved membrane and electrode assemblies for proton exchange membrane fuel cells

被引:48
作者
Iyuke, SE [1 ]
Mohamad, AB
Kadhum, AAH
Daud, WRW
Rachid, C
机构
[1] Univ Pertanian Malaysia, Dept Environm Chem & Engn, Fac Engn, Serdang 43400, Selangor DE, Malaysia
[2] Univ Kebangsaan Malaysia, Dept Chem & Proc Engn, Bangi 43600, Selangor DE, Malaysia
关键词
fuel cell; membrane and electrode assembly; hydrogen; irreversibility; optimization; platinum catalyst;
D O I
10.1016/S0378-7753(03)00016-8
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
Three electrodes-E1 (0.18 Mg Pt cm(-2)), E2 (0.38 Mg pt cm(-2)), E3 (0.4 Mg pt cm(-2) without a gas-diffusion layer)-are fabricated and compared with a commercial product (E-TEK). The performance of the electrodes increases with increase in Pt loading in the catalyst layer. The performance of the E2 electrode is superior to that of E1, E-TEK or E3. Elimination of the diffusion layer between the carbon-cloth substrate and the catalyst layer affects the performance of electrode E3 in particular. The power density shows a similar pattern to current density. The difference in performance between E2 and E-TEK electrodes may be due to the difference in the method of fabrication. Increase in exchange current density results in an increase in efficiency. The curves for E1, E2 and E-TEK electrodes appear to stabilize at constant efficiency, which indicates maximum efficiency at a lower exchange current density, compared with the E2 electrode, which does not approach a steady efficiency even at an exchange current density of 1 mA cm(-2). This means that the E2 electrode has greater efficiency than E1, E3 or E-TEK electrodes. Voltage and irreversibility curves for the four electrodes meet at different voltage operational limits; namely, 0.48, 0.55, 0.46 and 0.42 V at 1.2, 0.85, 0.4 and 0.3 mA cm(-2), for E-TEK, E2, E1 and E3 electrodes, respectively. Hence, while these electrodes can be operated conveniently, the E2 electrode with a 0.38 mg Pt cm-2 loading can be operated at optimum conditions of 0.55 V and 0.85 mA cm(-2). (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:195 / 202
页数:8
相关论文
共 9 条
[1]  
Buchi Felix N, 1997, J ELECTROCHEM SOC, V144, P2767
[2]  
LARMINIE J, 2001, FUEL CELL SYSTEMS EX, P17
[3]   EFFECT OF SPUTTERED FILM OF PLATINUM ON LOW PLATINUM LOADING ELECTRODES ON ELECTRODE-KINETICS OF OXYGEN REDUCTION IN PROTON-EXCHANGE MEMBRANE FUEL-CELLS [J].
MUKERJEE, S ;
SRINIVASAN, S ;
APPLEBY, AJ .
ELECTROCHIMICA ACTA, 1993, 38 (12) :1661-1669
[4]   Influence of the structure in low-Pt loading electrodes for polymer electrolyte fuel cells [J].
Passalacqua, E ;
Lufrano, F ;
Squadrito, G ;
Patti, A ;
Giorgi, L .
ELECTROCHIMICA ACTA, 1998, 43 (24) :3665-3673
[5]  
RACHID C, 2001, THESIS U KEBANGAAN M, P43
[6]  
SASI KG, 1994, ELECTROCHIM ACTA, V40, P285
[7]   METHODS TO ADVANCE TECHNOLOGY OF PROTON-EXCHANGE MEMBRANE FUEL-CELLS [J].
TICIANELLI, EA ;
DEROUIN, CR ;
REDONDO, A ;
SRINIVASAN, S .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1988, 135 (09) :2209-2214
[8]  
WILSON MS, 1995, ELECTROCHIM ACTA, V40, P355, DOI 10.1016/0013-4686(94)00272-3
[9]   WATER-UPTAKE BY AND TRANSPORT THROUGH NAFION(R) 117 MEMBRANES [J].
ZAWODZINSKI, TA ;
DEROUIN, C ;
RADZINSKI, S ;
SHERMAN, RJ ;
SMITH, VT ;
SPRINGER, TE ;
GOTTESFELD, S .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (04) :1041-1047