Self-exfoliation of 2D covalent organic frameworks: morphology transformation induced by solvent polarity

被引:40
|
作者
Zhang, Na [1 ]
Wang, Taisheng [1 ]
Wu, Xing [1 ]
Jiang, Chen [1 ]
Chen, Fang [1 ]
Bai, Wei [2 ]
Bai, Ruke [1 ]
机构
[1] Univ Sci & Technol China, Dept Polymer Sci & Engn, CAS Key Lab Soft Matter Chem, Hefei 230026, Anhui, Peoples R China
[2] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
基金
中国国家自然科学基金;
关键词
TRIAZINE-BASED FRAMEWORKS; 2-DIMENSIONAL POLYMER; CRYSTALLINE; NANOSHEETS; OXIDATION;
D O I
10.1039/c7ra09647j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, covalent organic nanosheets (CONs) have emerged as functional two-dimensional (2D) materials for versatile applications. Strong interaction among layers and the instability of borate ester in moisture are the major hurdles to obtain few layered boron-containing CONs by exfoliation of their bulk counterparts. In this paper, we report a facile approach for preparation of few layered borate ester-containing CONs based on electrostatic repulsion of ions. We incorporated organic ionic groups into porous covalent organic frameworks (COFs) and it has been proved that the COFs with quaternary ammonium group could self-exfoliate into few layered ionic covalent organic nanosheets (iCONs) in polar organic solvents. Interestingly, the morphology of the iCOFs-A could be changed from a multilayered aggregation to nanocapsules, or 2D sheets when solvents with different polarity were used. In contrast, non-ionic covalent organic frameworks COFs-B could not self-exfoliate in various solvents. In addition, the self-exfoliated nanosheets could be used to fabricate uniform thin films on SiO2 wafer and the film exhibited explicit optical and electrical properties.
引用
收藏
页码:3803 / 3808
页数:6
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