钋
氢氧化物
阳离子聚合
材料科学
膜
离子液体
化学工程
电化学
离子键合
共价键
氢氧化锌
离子电导率
锌
电化学储能
离子
纳米技术
无机化学
电极
化学
高分子化学
有机化学
超级电容器
电解质
工程类
冶金
生物化学
物理化学
催化作用
作者
Ye Tian,Xiaobin Hui,Kaiyu Wang,Yufei Yuan,Huanhuan Chen,Ki‐Taek Bang,Ran Tao,Rui Wang,Dong‐Myeong Shin,Yaozhong Lan,Zheng‐Long Xu,Yoonseob Kim
标识
DOI:10.1002/anie.202419257
摘要
Owing to their well‐defined crystalline pore structures and ordered functional ionic groups along the skeleton, ionic covalent organic frameworks (iCOFs) exhibit excellent performance and have significant potential for use in energy storage and conversion devices. Herein, we for the first time developed cationic phosphonium COFs with high hydroxide conduction even with low ion exchange capacity (IEC). Specifically, we synthesized COFs containing quaternary phosphonium groups as excellent ion transport moieties. Then, we fabricated freestanding phosphonium membranes through a vapor‐assisted method, which exhibited high hydroxide conductivity of 126 mS cm–1 at 80 °C from a minimal IEC of 1.17 mmol g–1. The resulting film was successfully applied to zinc–air batteries, demonstrating energy density of 96.1 mW cm–2, specific capacity of 95.0 mAh cm–2, and stable operation over 2,300 min. Overall, in addition to investigating a novel cationic functional group, we demonstrated a freestanding film formation method of COF‐based materials. The findings can provide a solid foundation for advancing the field of iCOFs to ion transport and promoting electrochemical applications.
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