化学
乙腈
纳米技术
共价键
氧化物
离解(化学)
胶体
膜
化学工程
亚胺
石墨烯
溶解度
动态共价化学
气体分离
溶剂化
水溶液
共价有机骨架
制作
纳米结构
组合化学
精细化工
选择性
一步到位
自组装
纳米颗粒
三元运算
氢甲酰化
纳米复合材料
欺骗
膜技术
纳米材料
模板
分离(统计)
作者
Guipeng Yu,Hu Cui,F Zhang,Lifeng Deng,Qingyang Zou,Junxi Shou,Xi Zhang,Shuai Gu,Pengpeng Shao,Juntao Tang
摘要
Two-dimensional covalent organic framework nanosheets (2D-CONs) have garnered significant attention in gas separation owing to their ultrathin nature and vertically aligned ordered nanopores. However, the efficient synthesis of CONs with high crystallinity, minimal defects, and large aspect ratios remains a major challenge. Herein, a scalable and rapid fabrication based on a “solvation-induced reassembly” strategy is developed to construct CONs with exceptional aspect ratios from colloidal particles, wherein water, acting as a poor solvent, plays a pivotal role in directing the assembly of nanospheres. Mechanism insights reveal that the pronounced difference in Hansen solubility parameters between water and acetonitrile enables water not only to disrupt the acetonitrile solvation shell and promote covalent organic framework (COF) colloid aggregation, but also to activate the reversible dissociation and reformation of imine bonds, thereby driving the transformation from nanospheres to nanosheets. The versatility of this method is demonstrated by the successful preparation of high aspect ratio CONs from a range of commonly used aldehydes. Membranes were fabricated by coassembling the as-produced CONs with graphene oxide (GO), and they achieved highly efficient H 2 /CO 2 separation performance that exceeds most reported COF-based separation membranes, significantly surpassing the 2008 Robeson upper bound. This study provides a versatile strategy for the controlled preparation of CONs and opens new avenues for the processing and integration of COF-based materials in advanced gas separation technologies.
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