Tao Wang, Duoying Chen, Chenxi Wang, Haibing Wei, Yunsheng Ding
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引用次数: 0
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.
期刊介绍:
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