芳烯
材料科学
耐久性
电解质
膜
化学工程
高分子化学
复合材料
有机化学
电极
化学
物理化学
生物化学
烷基
芳基
工程类
作者
Tao Wang,D. Chen,Chenxi Wang,Haibing Wei,Yunsheng Ding
标识
DOI:10.1002/adfm.202422504
摘要
Abstract The isomerization strategy is employed to enhance the alkaline stability of poly(arylene piperidinium)s (PAP) while maintaining the monomer commerciality and polymer architecture tunability. Isomeric poly(arylene piperidinium) ( i ‐PAP) exhibits improved alkali resistance relative to conventional PAP, as evidenced by ex situ alkaline stability and in situ cell durability tests. Following treatment in 10 m aqueous NaOH at 80 °C for 360 h or operation at 0.4 A cm −2 for 100 h in an anion exchange membrane fuel cell (AEMFC) prototype, the decomposition of the piperidinium moieties in i ‐PAP is ≈50% of that observed in PAP. Moreover, through a copolymerization strategy, the i ‐PAP‐88 membrane, which has suppressed water absorption, reaches a peak power density of 1.44 W cm −2 and demonstrates an in situ durability of 310 h. Furthermore, a noble metal‐free (anode) AEM water electrolyzer (AEMWE) achieves a high current density of 6.43 A cm⁻ 2 at 2.0 V and an excellent Faradaic efficiency of 98.3%. This study highlights a strategy for designing alkali‐stable polyelectrolytes that mitigate degradation during the operation of alkaline electrochemical devices.
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