材料科学
结晶
微型多孔材料
吸附
化学工程
亚胺
共价键
分散性
苯甲腈
共价有机骨架
三元运算
Crystal(编程语言)
单晶
纳米技术
扩散
溶剂
动力学
催化作用
堆积
水解
物理吸附
金属有机骨架
多相催化
聚合物
作者
Yixiao Ren,Jingtian Cheng,Jiao Xie,Wuyan Liu,Yulong Xu,Min Song,Yixuan Wu,Lifeng Chi,Guang Lü
出处
期刊:Small
[Wiley]
日期:2026-01-20
卷期号:22 (15): e09864-e09864
标识
DOI:10.1002/smll.202509864
摘要
The effective control over mesoscale features of covalent organic framework (COF) single crystals is important for definitive structural analysis, systematic structure-performance study, and elucidating crystallization mechanisms. However, the rapid synthesis of COF single crystals with uniform but flexibly tunable size remains a challenge on account of the complicated process of crystallization. Here, we report a dehydration-assisted modulated strategy enabling the rapid synthesis of single-crystalline imine-linked three-dimensional (3D) COFs (COF-300, COF-303, and COF-320). The strategy stems from a systematic study on the role of water in solvothermal and aniline-modulated syntheses of COF-300 using 1,4-dioxane as solvent. Kinetic analyses reveal that the hydrolysis reaction reduces the efficiency of the imine-exchange reaction in regulating the reversible imine bond formation, thereby retarding crystallization in modulated synthesis. Based on this finding, a dehydrated modulated strategy employing hydratable benzonitrile as solvent was developed and flexibly combined with simple adjustments to reaction temperature, solvent, and static/stirring conditions to achieve rapid synthesis of COF-300 single crystals with uniform size tunable from 213 nm to 44.3 µm within 1∼3 h. Crystal size-dependent iodine sorption measurements demonstrate that shortening microporous diffusion paths can accelerate adsorption/desorption kinetics and enhance sorption capacity.
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