膜
电解
共价键
共价有机骨架
聚合物
离子交换
化学
纳米孔
电导率
离子
肿胀 的
材料科学
极限抗拉强度
离子运输机
化学工程
芯(光纤)
高分子化学
电解水
水运
无机化学
工作(物理)
合成膜
机械强度
金属有机骨架
水处理
离子电导率
作者
Caili Yuan,Xiaoqin Ma,Zude Shen,Yuhang Chen,Xiaoli Lu,Wei Yuan,Li Li,Jianchuan Wang,Zidong Wei
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-07
卷期号:64 (48): e202513244-e202513244
被引量:8
标识
DOI:10.1002/anie.202513244
摘要
Abstract Covalent organic frameworks (COFs) offer well‐defined pores for efficient ion transport but suffer from poor mechanical stability. Herein, a sandwich‐like free‐standing COF‐based anion exchange membrane (COF‐AEM) is prepared, combining a COF core with in situ‐grown functional polymer layers. This strategy not only overcomes the polymer/COF incompatibility but also retains the intrinsic nanopores of the COF framework, enabling ion transport with a conductivity of 110 mS cm −1 at 80 °C under a remarkably low ion exchange capacity (IEC) (1.53 mmol g −1 ). Furthermore, the rigid and hydrophobic COF core effectively mitigates the membrane swelling ratio (SR) (5.2% @ 80 °C), while its combination with the flexible hydrophilic polymer skin enhances the robustness of the COF‐AEM simultaneously, achieving a tensile strength of 21.4 MPa. Demonstrated in alkaline water electrolysis, this represents the first free‐standing COF‐AEM for such applications. Our design expands COF‐AEM structural diversity, offering a promising approach for advanced ion‐conductive materials.
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