化学
结晶度
连接器
Crystal(编程语言)
多孔性
单体
共价键
单晶
化学工程
吸附
无定形固体
聚合物
晶体生长
纳米技术
结晶学
有机化学
材料科学
计算机科学
操作系统
工程类
程序设计语言
作者
Zhipeng Zhou,Xiao‐Hong Xiong,Lei Zhang,Yuyao Li,Yonghang Yang,Xin Dong,Dongyang Lou,Zhang‐Wen Wei,Wei Liu,Cheng‐Yong Su,Junliang Sun,Zhikun Zheng
摘要
The core features of covalent organic frameworks (COFs) are crystallinity and porosity. However, the synthesis of single-crystal COFs with monomers of diverse reactivity and adjustment of their pore structures remain challenging. Here, we show that linkers that can react with a node to form single-crystal COFs can guide other linkers that form either COFs or amorphous polymers with the node to gain single-crystal COFs with mixed components, which are homogeneous on the unit cell scale with controlled ratios. With the linker-guided crystal growth method, we created nine types of single-crystal COFs with up to nine different components, which are more complex than any known crystal. The structure of the crystal adapted approximately to that of the main component, and its pore volume could be expanded up to 8.8%. Different components lead to complex and diverse pore structures and offer the possibilities to gain positive synergies, as exemplified by a bicomponent COF with 2200 and 733% SO2 uptake capacity of that of the two pure-component counterparts at 298 K and 0.002 bar. The selectivity for separation of SO2/CO2 ranges from 1230 to 4247 for flue gas based on ideal adsorbed solution theory, recording porous crystals. The bicomponent COF also exhibits a 1300% retention time of its pure-component counterparts for SO2 in a dynamic column breakthrough experiment for deep desulfurization.
科研通智能强力驱动
Strongly Powered by AbleSci AI