质子交换膜燃料电池
微型多孔材料
腐蚀
材料科学
图层(电子)
化学工程
复合材料
扩散层
极化(电化学)
电化学
基质(水族馆)
接触角
电极
膜
化学
生物化学
物理化学
工程类
海洋学
地质学
作者
Keyi Xu,Qian Di,Fengman Sun,Ming Chen,H. Wang
出处
期刊:Fuel
[Elsevier]
日期:2023-11-07
卷期号:358: 130198-130198
被引量:7
标识
DOI:10.1016/j.fuel.2023.130198
摘要
Robust electrochemical corrosion of gas diffusion layers (GDL) in proton exchange membrane fuel cell (PEMFC) could cause significant decline of cell performance. However, the detailed mechanism still remains elusive. Herein, the structural characteristics of GDL after electrochemical accelerated stress test (AST) and sequent impacts on the mass-transfer performance of membrane electrode assemblies were explored. With the electrochemical corrosion duration increasing, polytetrafluoroethylene (PTFE) peeling and carbon fibers exposure were observed on substrate layer surface, while corrosion pores were detected on microporous layer (MPL). Both substrate layer and MPL experienced significant increase in surface roughness, which was reflected in the surface and bulk resistance. Surface contact angle and water permeability threshold tests showed that surface and internal hydrophobicity of GDL degraded comprehensively. More significant carbon corrosion in MPL and PTFE loss in substrate layer were revealed by X-ray photoelectron spectroscopy and thermogravimetric analysis. Collectively, worse power density and severe ohmic and mass-transfer polarization after AST were confirmed and the oxygen mass-transfer performance was analyzed in single-cell tests. This work clearly explains the distinctive degradation mechanisms of the substrate layer and MPL and provides guidance for the design and application of GDL.
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