离子液体
水溶液
相(物质)
热导率
质子
共价键
材料科学
热的
共价有机骨架
化学工程
化学
色谱法
有机化学
热力学
催化作用
复合材料
物理
工程类
量子力学
作者
Wenhui Yao,Yongkui Chen,Timing Fang,Xiaomin Liu,Xiao Zhao,Shuaiqi Gao,Zhiyong Li,Jianji Wang,Jianji Wang
标识
DOI:10.1021/acs.jpclett.3c02069
摘要
Covalent organic frameworks (COFs) have regular channels that can accommodate guest molecules to provide highly conductive solid electrolytes. However, designing smart, conductive COFs remains a great challenge. Herein, we report the first example of PEG-functionalized ionic liquids (ILs) anchored on the COF walls by strong hydrogen bonding to fabricate thermally responsive COFs (ILm@COF). We found that similar to the traditional IL/water mixture, the ILs undergo lower critical solution temperature (LCST)-type phase behavior within COF nanopores under high moisture levels. However, the phase separation temperature of aqueous IL decreases in COF channels due to the strong interaction between the IL and COF. Thus, the proton conductivity of ILm@COF can be reversibly switched by phase miscibility and separation in COF nanopores, and there is no obvious decrease even after 20 switching cycles. Our work provides important clues for understanding liquid-liquid phase separation in a confined nanospace and opens a new pathway to switchable proton conductivity.
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