聚合
阳离子聚合
单体
聚合物
离子电导率
氢氧化物
离子键合
离子交换
化学
膜
化学工程
高分子化学
材料科学
无机化学
有机化学
离子
电极
物理化学
工程类
电解质
生物化学
作者
Jesse H. Hsu,Cheyenne R. Peltier,Megan Treichel,Jamie C. Gaitor,Qihao Li,Renee Girbau,Alexandra J. Macbeth,Héctor D. Abruña,Kevin J. T. Noonan,Geoffrey W. Coates,Brett P. Fors
标识
DOI:10.1002/anie.202304778
摘要
Abstract The limited number of methods to directly polymerize ionic monomers currently hinders rapid diversification and production of ionic polymeric materials, namely anion exchange membranes (AEMs) which are essential components in emerging alkaline fuel cell and electrolyzer technologies. Herein, we report a direct coordination‐insertion polymerization of cationic monomers, providing the first direct synthesis of aliphatic polymers with high ion incorporations and allowing facile access to a broad range of materials. We demonstrate the utility of this method by rapidly generating a library of solution processable ionic polymers for use as AEMs. We investigate these materials to study the influence of cation identity on hydroxide conductivity and stability. We found that AEMs with piperidinium cations exhibited the highest performance, with high alkaline stability, hydroxide conductivity of 87 mS cm −1 at 80 °C, and a peak power density of 730 mW cm −2 when integrated into a fuel cell device.
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