膜
离子交换
化学
动力学
吸附
阳离子聚合
水运
化学工程
质子交换膜燃料电池
电解质
离子
热力学
高分子化学
有机化学
物理化学
环境科学
环境工程
吸附
工程类
物理
量子力学
生物化学
水流
电极
作者
Yiwei Zheng,Uri Ash,Ravi P. Pandey,Amobi G. Ozioko,Julia Ponce-González,Michael Handl,Thomas Weissbach,John R. Varcoe,Steven Holdcroft,Matthew W. Liberatore,Renate Hiesgen,Dario R. Dekel
出处
期刊:Macromolecules
[American Chemical Society]
日期:2018-04-17
卷期号:51 (9): 3264-3278
被引量:179
标识
DOI:10.1021/acs.macromol.8b00034
摘要
Anion exchange membrane fuel cells (AEMFCs) have attracted extensive attention in the recent years, primarily due to the distinct advantage potentials they have over the mainstream proton exchange membrane fuel cells. The anion exchange membrane (AEM) is the key component of AEMFC systems. Because of the unique characteristics of water management in AEMFCs, understanding the water mobility through AEMs is key for this technology, as it significantly affects (and limits) overall cell performances. This work presents a study of the equilibrium state and kinetics of water uptake (WU) for AEMs exposed to vapor source H2O. We investigate different AEMs that exhibit diverse water uptake behaviors. AEMs containing different backbones (fluorinated and hydrocarbon-based backbones) and different functional groups (various cations as part of the backbone or as pendant groups) were studied. Equilibrium WU isotherms are measured and fitted by the Park model. The influence of relative humidity and temperature is also studied for both equilibrium and dynamic WU. A characteristic time constant is used to describe WU kinetics during the H2O sorption process. To the best of our knowledge, this is the first time that WU kinetics has been thoroughly investigated on AEMs containing different backbones and cationic functional groups. The method and analysis described in this work provide critical insights to assist with the design of the next-generation anion conducting polymer electrolytes and membranes for use in advanced high-performance AEMFCs.
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