膜
离子
渗透
化学物理
选择性
存水弯(水管)
相(物质)
离子阱
扩散
分子动力学
化学
基质(化学分析)
化学工程
分析化学(期刊)
材料科学
计算化学
色谱法
有机化学
热力学
物理
工程类
环境工程
生物化学
催化作用
作者
Meidi Wang,Tianyu Ma,Zhuo‐Hao Wu,Yawei Liu,Shuang Li,Zixuan Cheng,Xue‐Qian Wu,Bojing Sun,Zhongyi Jiang,Dong‐Sheng Li
标识
DOI:10.1002/anie.202504990
摘要
Artificial molecular/ion traps afford grand potential in membrane‐based separation processes. However, the existing trap‐based architectures often confer over‐strong binding forces, which severely impedes the release of bound solutes during their transmembrane diffusion processes. Herein, we propose an unprecedented local‐ion trap bearing moderate binding force and additional repulsion force in a type of phase‐reversed mixed matrix covalent organic framework (PRCOF) membranes. By implementing COF as continuous phase and polymer as dispersed phase at molecular level, the local‐ion trap is formed in the COF channels equipped with free amino groups from polyethyleneimine (PEI). This unique local‐ion trap built by electronegative COF nano‐domains and electropositive PEI nano‐domains, offers appropriate interaction towards Li+, which allows the precise recognition and rapid transport of Li+ in the membrane channels. By tuning the microenvironments of local‐ion trap, the optimum PRCOF‐1 membrane exhibits considerably high actual selectivity of 190 along with rapid Li+ permeation rate of 0.262 mol h‐1 m‐2 in dealing with a Li+/Mg2+ binary mixture. This work provides in‐depth insights into the design of high‐performance membranes with appropriate chemical interactions.
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