单层
膜
剥脱关节
材料科学
纳米片
共价有机骨架
化学工程
单体
石墨烯
阳离子聚合
复合数
氧化物
纳米技术
高分子化学
复合材料
聚合物
化学
冶金
工程类
生物化学
多孔性
作者
Jie Zhang,Xiaofeng Li,Feng Yang,Zhengdong Ouyang,Pan He,Zhimin Jia,Honghan Long,Ningning He,Yingdan Zhang,Yingdi Zou,Bo Jiang,Ziqian Han,Guo‐Hong Tao,Ning Liu,Yang Li,Lijian Ma
标识
DOI:10.1021/acsami.4c14803
摘要
The efficient preparation of two-dimensional large-sized monolayer covalent organic framework (COF) nanosheets for highly permeable membranes has posed a long-standing challenge in the COF field. While the self-exfoliation of charged COFs represents a promising method for nanosheet production, its efficiency requires further enhancement. In this study, we present a novel finding that the presence of hydroxyl groups on the monomer significantly influences the self-exfoliation efficiency of charged COFs. Through precise regulation of hydroxyl group numbers on the monomers, we successfully achieved the efficient fabrication of large monolayer cationic COF nanosheets with impressive solubilities in common organic solvents. By virtue of their positive charge, COF monolayer nanosheets rapidly interacted with negatively charged monolayer graphene oxide (GO) in solution, facilitating their assembly into interlaced composite membranes through electrostatic interactions. The composite membranes benefited from the strong Coulombic attraction between the COF and GO nanosheets, leading to enhanced membrane stability, while the shielding effect of GO on the COF pores contributed to improved size sieving efficiency. This innovative strategy enabled the composite membranes to achieve highly selective separation of ReO4– and MoO42–, with a remarkable 100% interception rate for MoO42–.
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