Development of high-power electrodes for a liquid-feed direct methanol fuel cell

被引:95
作者
Lim, C
Wang, CY [1 ]
机构
[1] Penn State Univ, Dept Mech Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Mat Sci & Engn, Electrochem Engine Ctr, ECEC, University Pk, PA 16802 USA
基金
美国国家科学基金会;
关键词
direct methanol fuel cells; membrane-electrode assembly (MEA); polymer electrolytes; high power;
D O I
10.1016/S0378-7753(02)00541-4
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
Based upon Nafion 112 membrane, membrane-electrode assemblies for a liquid-feed direct methanol fuel cell (DMFC) were fabricated by using a novel method of modified Nation solution and tape-casting, with unsupported Pt-Ru as an anode catalyst and carbon supported 40 wt.% Pt as a cathode catalyst. The amounts of catalyst loading were controlled to be 4 mg/cm(2) in the anode and 1.3 mg/cm(2) in the cathode. Morphological characteristics of anode and cathode were examined by scanning electron microscopy (SEM). A time-delayed activation effect was found in single cell tests and attributed to time-dependent wetting behavior of Nation polymers within both catalyst layers. A high compression of the single cell leads to a remarkable decrease in diffusion-limiting current density, caused by hydrophilic broken fibers and cleavage-like defects generated during excessive compression of the cell. A maximum power density of 0.21 W/cm(2) is achieved in 2 M CH3OH solution at 90 degreesC under the operating condition of non-pressurized anode side and non-humidified air pressurized to 15 psi. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:145 / 150
页数:6
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