Correlating Catalyst Growth with Liquid Water Distribution in Polymer Electrolyte Fuel Cells

被引:1
作者
Sharma, Preetam [1 ]
Aaron, Douglas [1 ]
Boillat, Pierre [2 ]
Cheng, Lei [3 ]
Johnston, Christina [3 ]
Mench, Matthew M. [1 ]
机构
[1] Univ Tennessee, Dept Mech Aerosp & Biomed Engn, Electrochem Energy Storage & Convers Lab, Knoxville, TN 37919 USA
[2] Paul Scherrer Inst PSI, Lab Neutron Scattering & Imaging, Forschungsstr 111, CH-5232 Villigen, Switzerland
[3] Bosch Res & Technol Ctr, Sunnyvale, CA 94085 USA
关键词
accelerated stress test (AST); catalyst growth; fuel cells; neutron imaging; water distribution; ACCELERATED DEGRADATION; MEMBRANE DEGRADATION; PHYSICAL DEGRADATION; QUANTIFICATION; NANOPARTICLES; ASSEMBLIES; MECHANISMS; TRANSPORT; IMPACT; PEMFC;
D O I
10.1002/smll.202404023
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study investigates the impact of liquid water distribution in a polymer electrolyte fuel cell (PEFC) on the spatially heterogeneous platinum (Pt) catalyst degradation. The membrane electrode assemblies (MEAs) are aged using accelerated stress tests (ASTs) in varied cathode gas environments (N2 and air) to instigate Pt catalyst degradation. The study employs high-resolution neutron imaging and synchrotron micro-X-ray diffraction (micro-XRD) to map liquid water distribution and Pt particle size, respectively. Neutron radiographs reveal liquid water accumulation primarily within the diffusion media, especially under flow field lands, due to thermal resistance differences between channels and lands. Aged MEAs exhibit increased water retention, likely due to increased hydrophilicity of the diffusion media with aging. Synchrotron micro-XRD maps unveil significant heterogeneity in Pt particle size distribution in the aged MEAs, correlated with preferential liquid water accumulation under flow field lands. This study highlights the critical role of flow field design and water distribution in catalyst degradation, underscoring the need for innovative strategies to enhance fuel cell durability and performance.
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页数:14
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