磷酸
电解质
膜
聚合物
化学工程
离聚物
化学
无机化学
有机化学
电极
工程类
共聚物
生物化学
物理化学
作者
Katie Heeyum Lim,Ivana Matanović,Sandip Maurya,Youngkwang Kim,Youngkwang Kim,Emory S. De Castro,Ji‐Hoon Jang,Hyounmyung Park,Yu Seung Kim,Yu Seung Kim
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-12-15
卷期号:8 (1): 529-536
被引量:56
标识
DOI:10.1021/acsenergylett.2c02367
摘要
Phosphoric acid loss poses immense hurdles for the durability of high-temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Here we report quaternary ammonium-biphosphate ion-pair HT-PEMFCs that do not lose phosphoric acids under normal and accelerated stress conditions. Our energetics study explains the acid loss behavior of the conventional phosphoric acid-polybenzimidazole (PA-PBI) system by two mechanisms. If PA loss occurs via acid evaporation, the acid loss is constant over time. On the other hand, when water activity in the PA-PBI system is high, exponential decay of PA loss occurs via the water replacement mechanism. Combined 31P NMR and computational studies show that the proposed ion-pair system has six times higher interaction energy, which allows for containing all PAs in the membrane electrode assemblies under a broad range of operating conditions. In addition, polar interactions between the phosphonic acid ionomer and phosphoric acid explain acid retention in the electrodes of the ion-pair HT-PEMFCs.
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