共价有机骨架
共价键
材料科学
膜
微晶
纳米技术
工作(物理)
可扩展性
埃
危险废物
接口(物质)
分子
分子动力学
化学工程
聚合物
金属有机骨架
化学物理
纳米尺度
盐(化学)
纳滤
作者
S N Fang,Yu Liao,Jia-Hao Tang,Mingxiu Tang,Fuxin Zheng,Zhenxiang Pan,Yingnan Feng,Gang Han
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-12-19
卷期号:11 (51): eaeb0929-eaeb0929
被引量:4
标识
DOI:10.1126/sciadv.aeb0929
摘要
This work addresses the long-standing challenge of insufficient permselectivity in two-dimensional (2D) covalent organic framework (COF) membranes by developing a generalizable and potentially scalable self-templating interfacial assembly method to synthesize vertically aligned 2D COF polycrystalline nanofilms. Experiments and molecular simulations reveal that molecular amphiphilicity-driven spontaneous confinement and directional alignment of framework-building units at the organic/aqueous interface instigate the vertical growth of COF monolayers. The superior sieving ability of sub-4 angstrom interlayer nanochannels enables vertically aligned COF membranes to efficiently intercept salt ions, electrically neutral small molecules, and hazardous chemicals, outperforming conventional COF membranes. The implemented strategy can be extended to other building blocks and framework topologies, opening up avenues for fine-tuning the pore structure of 2D COF membranes.
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