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具有高效碘吸附性能的共价有机框架有序大孔-微孔单晶

Ordered Macro-Microporous Single Crystals of Covalent Organic Frameworks with Efficient Sorption of Iodine.

作者信息

Liu Tong, Zhao Yi, Song Min, Pang Xinghan, Shi Xiaofei, Jia Jingjing, Chi Lifeng, Lu Guang

机构信息

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou 215123, China.

出版信息

J Am Chem Soc. 2023 Feb 1;145(4):2544-2552. doi: 10.1021/jacs.2c12284. Epub 2023 Jan 20.

Abstract

Fashioning microporous covalent organic frameworks (COFs) into single crystals with ordered macropores allows for an effective reduction of the mass transfer resistance and the maximum preservation of their intrinsic properties but remains unexplored. Here, we report the first synthesis of three-dimensional (3D) ordered macroporous single crystals of the imine-linked 3D microporous COFs (COF-300 and COF-303) via a template-assisted modulated strategy. In this strategy, COFs crystallized within the sacrificial colloidal crystal template, assembled from monodisperse polystyrene microspheres, and underwent an aniline-modulated amorphous-to-crystalline transformation to form large single crystals with 3D interconnected macropores. The effects of the introduced macroporous structure on the sorption performances of COF-300 single crystals were further probed by iodine. Our results indicate that iodine adsorption occurred in micropores of COF-300 but not in the introduced macropores. Accordingly, the iodine adsorption capacity of COF single crystals was governed by their micropore accessibility. The relatively long diffusion path in the non-macroporous COF-300 single crystals resulted in a limited micropore accessibility (48.4%) and thus a low capacity in iodine adsorption (1.48 g·g). The introduction of 3D ordered macropores can greatly shorten the microporous diffusion path in COF-300 single crystals and thus render all their micropores fully accessible in iodine adsorption with a capacity (3.15 g·g) that coincides well with the theoretical one.

摘要

将微孔共价有机框架(COF)制成具有有序大孔的单晶,可有效降低传质阻力并最大程度地保留其固有特性,但这一点尚未得到探索。在此,我们报告了通过模板辅助调制策略首次合成亚胺连接的三维(3D)微孔COF(COF-300和COF-303)的三维有序大孔单晶。在该策略中,COF在由单分散聚苯乙烯微球组装而成的牺牲性胶体晶体模板内结晶,并经历苯胺调制的非晶态到晶态转变,以形成具有三维互连大孔的大单晶。通过碘进一步探究了引入的大孔结构对COF-300单晶吸附性能的影响。我们的结果表明,碘吸附发生在COF-300的微孔中,而不是在引入的大孔中。因此,COF单晶的碘吸附容量取决于其微孔可及性。在无大孔的COF-300单晶中相对较长的扩散路径导致有限的微孔可及性(48.4%),从而导致碘吸附容量较低(1.48 g·g)。引入三维有序大孔可大大缩短COF-300单晶中的微孔扩散路径,从而使它们的所有微孔在碘吸附中完全可及,其容量(3.15 g·g)与理论值非常吻合。

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