Experimental study of cell reversal of a high temperature polymer electrolyte membrane fuel cell caused by H2 starvation

被引:39
作者
Zhou, Fan [1 ]
Andreasen, Soren Juhl [1 ]
Koer, Soren Knudsen [1 ]
机构
[1] Aalborg Univ, Dept Energy Technol, DK-9220 Aalborg, Denmark
关键词
H-2; starvation; HT-PEM fuel cell; Cell reversal; Current density distribution; GAS-DIFFUSION ELECTRODE; PHOSPHORIC-ACID; CATALYST LAYER; DEGRADATION; PEMFC; PERFORMANCE;
D O I
10.1016/j.ijhydene.2015.03.148
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
Operation under fuel starvation has been proved to be harmful to the fuel cell by causing severe and irreversible degradation. To characterize the behaviors of the high temperature PEM fuel cell under fuel starvation conditions, the cell voltage and local current density is measured simultaneously under different H-2 stoichiometries below 1.0 and at different current loads. The experimental results show that the cell voltage decreases promptly when the H-2 stoichiometry decreases to below 1.0. Negative cell voltage can be observed which indicates cell reversal. The local current density starts to diverge when the cell voltage decreases. In the H-2 upstream regions the current densities show an increasing trend, while those in the H-2 downstream regions show a decreasing trend. Consequently, the current density distribution becomes very uneven. The current density is the highest in the upstream regions, decreasing along the flow channel direction, becoming the lowest in the downstream regions. In addition, the CO2 and even the O-2 can be detected in the anode exhaust under fuel starvation conditions, confirming the occurring of carbon corrosion and water electrolysis reactions. With lower H-2 stoichiometry and higher current load, the cell voltage decrease rate is higher and the cell reversal is more severe. Higher CO2 concentration in anode exhaust is measured under these conditions, suggesting the degradation is more severe. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6672 / 6680
页数:9
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