网络拓扑
共价键
拓扑(电路)
材料科学
结晶
纳米技术
平面的
微型多孔材料
计算机科学
化学
数学
复合材料
组合数学
操作系统
计算机图形学(图像)
有机化学
作者
Dongyang Zhu,Yifan Zhu,Yu Chen,Qianqian Yan,Han Wu,Chun-Yen Liu,Xu Wang,Lawrence B. Alemany,Guanhui Gao,Thomas P. Senftle,Yongwu Peng,Xiaowei Wu,Rafael Verduzco
标识
DOI:10.1038/s41467-023-38538-x
摘要
Abstract Three-dimensional (3D) covalent organic frameworks (COFs) possess higher surface areas, more abundant pore channels, and lower density compared to their two-dimensional counterparts which makes the development of 3D COFs interesting from a fundamental and practical point of view. However, the construction of highly crystalline 3D COF remains challenging. At the same time, the choice of topologies in 3D COFs is limited by the crystallization problem, the lack of availability of suitable building blocks with appropriate reactivity and symmetries, and the difficulties in crystalline structure determination. Herein, we report two highly crystalline 3D COFs with pto and mhq-z topologies designed by rationally selecting rectangular-planar and trigonal-planar building blocks with appropriate conformational strains. The pto 3D COFs show a large pore size of 46 Å with an extremely low calculated density. The mhq-z net topology is solely constructed from totally face-enclosed organic polyhedra displaying a precise uniform micropore size of 1.0 nm. The 3D COFs show a high CO 2 adsorption capacity at room temperature and can potentially serve as promising carbon capture adsorbents. This work expands the choice of accessible 3D COF topologies, enriching the structural versatility of COFs.
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