Effect of Commercial Gas Diffusion Layers on Catalyst Durability of Polymer Electrolyte Fuel Cells in Varied Cathode Gas Environment

被引:10
|
作者
Khedekar, Kaustubh [1 ,2 ]
Satjaritanun, Pongsarun [2 ,3 ]
Stewart, Sarah [4 ]
Braaten, Jonathan [4 ]
Atanassov, Plamen [1 ,2 ,3 ]
Tamura, Nobumichi [5 ]
Cheng, Lei [4 ]
Johnston, Christina M. [4 ]
Zenyuk, Iryna, V [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Mat Sci & Engn, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Natl Fuel Cell Res Ctr, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Chem & Biomol Engn, Irvine, CA 92697 USA
[4] Bosch Res & Technol Ctr North Amer, Sunnyvale, CA 94085 USA
[5] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
关键词
catalyst degradation; gas diffusion layers; hydrogen; polymer electrolyte fuel cells; OXYGEN-TRANSPORT; DEGRADATION; IMPACT; COMPRESSION; PLATINUM;
D O I
10.1002/smll.202201750
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gas diffusion layers (GDLs) play a crucial role in heat transfer and water management of cathode catalyst layers in polymer electrolyte fuel cells (PEFCs). Thermal and water gradients can accelerate electrocatalyst degradation and therefore the selection of GDLs can have a major influence on PEFC durability. Currently, the role of GDLs in electrocatalyst degradation is poorly studied. In this study, electrocatalyst accelerated stress test studies are performed on membrane electrode assemblies (MEAs) prepared using three most commonly used GDLs. The effect of GDLs on electrocatalyst degradation is evaluated in both nitrogen (non-reactive) and air (reactive) gas environments at 100% relative humidity. In situ electrochemical characterization and extensive physical characterization is performed to understand the subtle differences in electrocatalyst degradation and correlated to the use of different GDLs. Overall, no difference is observed in the electrocatalyst degradation due to GDLs based on polarization curves at the end of life. But interestingly, MEA with a cracked microporous layer (MPL) in the GDL exhibited a higher electrocatalyst loading loss, which resulted in a lower and more heterogeneous increase in the average electrocatalyst nanoparticle size.
引用
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页数:12
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