4.7 Article

The buffer microporous layer improved water management for proton exchange membrane fuel cell at varying humidification

Journal

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
Volume 928, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2022.117072

Keywords

Proton exchange membrane fuel cell; Gas diffusion layer; Water management; Varying humidification; Buffer microporous layer

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This study improves the water management issue of proton exchange membrane fuel cells (PEMFCs) by enhancing the peak power density of the membrane electrode assembly (MEA) through a cathode hydrophobic microporous layer with added pore forming agent and a buffer microporous layer sprayed over the commercial gas diffusion layer (GDL). The optimized MEA shows a 36.8% increase in peak power density and improved performance under humidity changes, due to efficient water retention capacity and enhanced catalyst layer (CL) wettability.
Proton exchange membrane fuel cells (PEMFCs) are projected to be extensively deployed in different vehicle circumstances, with one of the primary issues being the water management of microporous layers. In this work, the sprayed cathode hydrophobic microporous layer with added pore forming agent has a substantially greater drainage capability than the commercial gas diffusion layer (GDL), significantly enhancing the peak power density of the membrane electrode assembly (MEA). In view of the membrane dehydration of MEA under typical vehicle humidification conditions, a buffer microporous layer (BMPL) comparable in structure to the anode catalyst layer (ACL) is sprayed over the commercial GDL as the anode water-retention GDL. The MEA performs considerably better than the MEA with commercial GDL. The peak power density improved by 36.8%, and its performance is less susceptible to humidity changes. This efficient water retention capacity assures the catalyst layer's (CL) wettability and speeds up hydrogen activation and proton transfer. Furthermore, this GDL preparation and optimization procedure is straightforward, the cost is manageable, and it has actual application value. This work proposes a novel technique for cathode and anode GDL matching, as well as commercial GDL customization.

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