超分子化学
膜
多孔性
氢键
离子液体
离子键合
共价键
材料科学
化学工程
分子
聚电解质
热的
聚合物
纳米技术
高分子化学
化学
化学物理
有机化学
复合材料
热力学
离子
催化作用
工程类
物理
生物化学
作者
Yue Shao,Yong‐Lei Wang,Xiangshuai Li,Atefeh Khorsand Kheirabad,Qiang Zhao,Jiayin Yuan,Hong Wang
标识
DOI:10.1002/anie.202002679
摘要
Abstract Reversible regulation of membrane microstructures via non‐covalent interactions is of considerable interest yet remains a challenge. Herein, we discover a general one‐step approach to fabricate supramolecular porous polyelectrolyte membranes (SPPMs) from a single poly(ionic liquid) (PIL). The experimental results and theoretical simulation suggested that SPPMs were formed by a hydrogen‐bond‐induced phase separation of a PIL between its polar and apolar domains, which were linked together by water molecules. This unique feature was capable of modulating microscopic porous architectures and thus the global mechanical property of SPPMs by a rational design of the molecular structure of PILs. Such SPPMs could switch porosity upon thermal stimuli, as exemplified by dynamically adaptive transparency to thermal fluctuation. This finding provides fascinating opportunities for creating multifunctional SPPMs.
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