Effect of catalyst layer microstructures on performance and stability for high temperature polymer electrolyte membrane fuel cells

被引:29
|
作者
Zhang, Jujia [1 ]
Wang, Haining [1 ]
Li, Wen [1 ]
Zhang, Jin [1 ]
Lu, Di [1 ]
Yan, Wenrui [1 ]
Xiang, Yan [1 ]
Lu, Shanfu [1 ]
机构
[1] Beihang Univ, Sch Space & Environm, Beijing Key Lab Bioinspired Energy Mat & Devices, Beijing 100191, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Catalyst layer; Microstructures; Pt utilization; Distribution of relaxation times analysis; Mass transfer; High temperature polymer electrolyte membrane fuel cell; IMPEDANCE; CO;
D O I
10.1016/j.jpowsour.2021.230059
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 microstructures of catalyst layers (CLs) provide the paths for phosphoric acid (PA) invasion and decide the amount and distribution of PA in CLs, which is essential to improve the performance and stability of high temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). In this work, the CLs with different microstructures are constructed and the effects of Pt loading on the performance and degradation of HT-PEMFCs are studied. The results show the CLs with flat surface slow down the process of PA invasion and well-developed pore structures promote the redistribution of PA, which results in low mass transfer resistance. Therefore, the peak power density of HT-PEMFC based on CLs prepared by ultrasonic-spraying is 1.4 times than that by screenprinting, while the performance degradation is only 11% after accelerated stress test of 30,000 cycles with the Pt loading of 0.5 mg cm-2. Distribution of relaxation times analysis is used to assist the electrochemical impedance spectroscopy to further distinguish the different physicochemical process within cells. The result reveals that mass transfer is affected greatly by the effects of microstructures and Pt loadings, and gets deterioration gradually with the invasion of PA into CLs, which not only makes Pt particle growth but decreases kinetics of oxygen reduction reaction.
引用
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页数:11
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