微型多孔材料
材料科学
电解
膜
化学工程
金刚烷
离子交换
电化学
水溶液
氢氧化物
碱性燃料电池
无机化学
聚合物
高分子化学
碱性水电解
侧链
质子交换膜燃料电池
膜电极组件
共轭微孔聚合物
核化学
电极
金属氢氧化物
电导率
功率密度
多孔性
电解水
作者
Xin Lan,Dongrui Chu,Mengjie Gu,Xinran Wang,Xiaojuan Zhang,Basheer Mansoor,Yi Xing,Nanwen Li,Lei Liu
标识
DOI:10.1021/acsami.6c01509
摘要
Microporous anion exchange membranes (AEMs) featuring rapid and selective ion–water transport have been extensively employed in various electrochemical devices, including AEM water electrolysis (AEMWE), AEM fuel cells (AEMFC), and aqueous flow batteries. Traditionally, the synthesis of microporous polymers has predominantly been dependent on the integration of bulky and twisted structural units within the polymer backbone. In this work, we introduce an efficient approach for fabricating microporous poly(terphenyl piperidinium) AEMs by the grafting of bulky adamantane side chains. Two series of adamantane-grafted AEMs, derived from poly( p -terphenyl piperidinium) (PTP) and poly( m -/ p -terphenyl piperidinium) ( m PTP) polymers, were synthesized, exhibiting an enhanced fraction of free volume and subsequently high λ-normalized hydroxide conductivity. The incorporation of adamantane markedly enhanced the membranes’ resistance to degradation under alkaline and oxidative conditions, and the m PTP-ada-15 membrane demonstrated a 15% reduction in conductivity and an 18% decrease in dry weight after 1360 and 240 h of immersion in 1 M NaOH at 80 °C and in Fenton’s reagent, respectively. Furthermore, the microporous AEMs functionalized with adamantane side chains exhibited superior performance in AEMFCs and AEMWEs relative to their ungrafted analogues, achieving a peak power density of 1230 mW cm –2 and a current density of 4.47 A cm –2 at 2.0 V for the m PTP-ada-15 membrane.
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