Model- and Theory-Based Evaluation of Pt Dissolution for Supported Pt Nanoparticle Distributions under Potential Cycling

被引:38
作者
Rinaldo, Steven G. [1 ,2 ]
Lee, Wendy [2 ]
Stumper, Juergen [2 ]
Eikerling, Michael [1 ]
机构
[1] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
[2] Automot Fuel Cell Cooperat Corp, 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
PEM FUEL-CELL; CATALYST DEGRADATION; PLATINUM DISSOLUTION; PEFC CATHODE; DURABILITY; ELECTRODES; SURFACES; PT/C; VOLTAMMETRY; INSTABILITY;
D O I
10.1149/1.3548504
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Pt dissolution is a leading cause of performance degradation in polymer electrolyte fuel cells, however, the mechanisms leading to accelerated Pt dissolution during potential cycling are unclear. In a new diagnostic application of our previously developed potentiostatic nanoparticle dissolution model, we outline here the use of the model as a method for determining the fundamental dissolution rate parameters that may control potential cycling induced electrochemically active surface area loss for supported Pt nanoparticles. We furthermore provide a pertinent foundation for the development of concerted experimental, theoretical, and modeling approaches for unraveling the mechanisms behind accelerated Pt dissolution. (C) 2011 The Electrochemical Society. [DOI: 10.1149/1.3548504] All rights reserved.
引用
收藏
页码:B47 / B49
页数:3
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