Study of the effect of temperature on Pt dissolution in polymer electrolyte membrane fuel cells via accelerated stress tests

被引:44
作者
Dhanushkodi, S. R. [1 ,2 ]
Kundu, S. [2 ]
Fowler, M. W. [1 ]
Pritzker, M. D. [1 ]
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[2] Automot Fuel Cell Cooperat, Burnaby, BC V5J 5J8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Accelerated stress testing; Fuel cell catalyst; Durability; Voltage loss analysis; Electrochemical surface area; ELECTROCATALYST DURABILITY; PLATINUM DISSOLUTION; DEGRADATION; CATALYST; PEMFCS; DEPOSITION; COMPONENTS; STABILITY; HYDROGEN;
D O I
10.1016/j.jpowsour.2013.07.016
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 of polymer electrolyte membrane fuel cells (PEMFC) at higher cell temperatures accelerates Pt dissolution in the catalyst layer. In this study, a Pt dissolution accelerated stress testing protocol involving the application of a potentiostatic square-wave with 3 s at 0.6 V followed by 3 s at 1.0 V was developed to test fuel cell membrane electrode assemblies (MEAs). The use of this Pt dissolution protocol at three different temperatures (40 degrees C, 60 degrees C and 80 degrees C) was investigated for the same membrane electrode assembly composition. Impedance analysis of the membrane electrode assemblies showed an increase in polarization resistance during the course of the accelerated stress testing. Polarization analysis and electrochemical active surface area (ECSA) loss measurements revealed evidence of increased cathode catalyst layer (CCL) degradation due to. Pt dissolution and deposition in the membrane as the cell temperature was raised. Scanning electron microscope (SEM) images confirmed the formation of Pt bands in the membrane. A diagnostic expression was developed to estimate kinetic losses due to oxygen reduction using the effective platinum surface area (EPSA) estimated from cyclic voltammograms. The results indicated that performance degradation occurred mainly due to Pt loss. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:1035 / 1045
页数:11
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