Revealing the critical role of low voltage excursions in enhancing PEM fuel cell catalyst degradation by automotive hydrogen/air potential cycling experiments

被引:4
|
作者
Colombo, Elena [1 ]
Casalegno, Andrea [1 ]
Guetaz, Laure [2 ]
Baricci, Andrea [1 ]
机构
[1] Politecn Milan, Dept Energy, Via Lambruschini 4, I-20156 Milan, Italy
[2] Univ Grenoble Alpes, CEA, LITEN, 17 Rue Martyrs, F-38054 Grenoble, France
关键词
Proton exchange membrane fuel cell; Catalyst degradation; Accelerated stress test; Voltage cycling; Short-stops; Nanoparticles growth; PLATINUM DISSOLUTION; SURFACE-AREA; PERFORMANCE; DURABILITY; IMPACT; PT/C; ELECTROCATALYSTS; TEMPERATURE; INSTABILITY; MECHANISMS;
D O I
10.1016/j.ijhydene.2024.03.373
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
The durability of Polymer Electrolyte Membrane Fuel Cells under dynamic operation still needs to be improved. To understand the automotive voltage cycling -induced catalyst degradation, the loss of the electrochemically active surface area (ECSA) is investigated through an experimental campaign on Membrane Electrode Assemblies. Ad -hoc hydrogen/air accelerated protocols were designed to evaluate the voltage profile impact in a range relevant for both automotive and heavy duty transport application ( <0.90 V). Besides the well-known aging dependence on the upper potential limit, this work evidences the critical role of the short-stops, characterized by low voltage transients. Effort was spent in studying this procedure parameters (voltage level, duration, scan rate, humidification). The accelerated ECSA loss is due to Pt nanoparticles coarsening as proved by transmission electron microscopy and is suspected dominated by Pt cathodic dissolution, incentivized during excursions towards very low potentials ( <0.4 V). These findings help the development of system mitigation strategies.
引用
收藏
页码:292 / 307
页数:16
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