质子交换膜燃料电池
膜电极组件
阴极
材料科学
化学工程
膜
离聚物
电极
电化学
复合材料
电解质
化学
聚合物
共聚物
生物化学
物理化学
工程类
作者
Lei Liu,Zhiyong Fu,Yijing Xing,Yifan Li,Zhuoqun Li,Haibin Li
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-09-03
卷期号:37 (18): 14315-14323
被引量:1
标识
DOI:10.1021/acs.energyfuels.3c02168
摘要
The preparation method of membrane electrode assemblies (MEAs) is a key factor that determines their electrochemical performance and lifespan. In this study, we develop a novel preparation method based on a wet-combining interface forming strategy for fabricating a high-performance MEA with an ultrathin proton exchange membrane (PEM). Through this method, an integrated MEA (R-MEA), assembled with an ultrathin (<10 μm) membrane reinforced with expanded polytetrafluoroethylene (ePTFE), is fabricated. In the wet-combining process, the liquid perfluorosulfonic acid (PFSA) ionomer sufficiently adheres to the surface of the three-dimensional (3D) catalyst layer (CL) of the gas diffusion electrode (GDE), thus forming a 3D coupling interface between the PEM and the cathode CL. Such a tight 3D PEM/cathode CL interface enlarges the contact area between the PEM and the cathode CL, thereby increasing the triple-phase boundary for the oxygen reduction reaction. On this basis, the novel R-MEA exhibits a significantly higher electrochemical surface area and a superior power performance compared to a conventional MEA (C-MEA) prepared by the catalyst-coated membrane method. Furthermore, the introduction of the ePTFE reinforcement in the PEM makes R-MEA possess a hydrogen crossover current close to that of C-MEA (which has a commercial GORE-SELECT membrane as its PEM). After 1000 cycles of wet/dry conditions, the R-MEA still maintains its superior power performance and a stable hydrogen crossover current, thus demonstrating its excellent mechanical durability.
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