Electrochemical impedance investigation of proton exchange membrane fuel cells experienced subzero temperature

被引:42
作者
Hou, Junbo
Song, Wei
Yu, Hongmei
Fu, Yu
Shao, Zhigang
Yi, Baolian
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Fuel Cell Syst & Engn Lab, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
关键词
proton exchange membrane (PEM) fuel cell; subzero; electrochemical impedance spectroscopy; mass transport; oxygen reduction reaction; agglomerate; COLD START; ELECTRODES; BEHAVIOR;
D O I
10.1016/j.jpowsour.2007.07.015
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
Polarization losses of the fuel cells with different residual water amount frozen at subzero temperature were investigated by electrochemical impedance spectroscopy (EIS) taking into account the ohmic resistance, charge transfer process, and oxygen mass transport. The potential-dependent impedance before and after eight freeze/thaw cycles suggested that the ohmic resistance did not change, while the change of the charge transfer resistance greatly depended on the residual water amount. Among the four cells, the mass transport resistance of the cell with the largest water amount increased significantly even at the small current density region. According to the thin film-flooded agglomerate model, the interfacial charge transfer process and oxygen mass transport within the agglomerate and through the ionomer thin film in the catalyst layer both contributed to the high frequency impedance arc. From the analysis of the Tafel slopes, the mechanism of the oxygen reduction reaction (ORR) was the same after the cells experienced subzero temperature. The agglomerate diffusion changed a little in all cells and the thin film diffusion effect was obvious for the cell with the largest residual water amount. These results indicated that the slower oxygen diffusion within the catalyst layer (CL) was the main contributor for the evident performance loss after eight freeze/thaw cycles. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:610 / 616
页数:7
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