微型多孔材料
等结构
材料科学
氢气储存
金属有机骨架
氢
选择性
分子
金属
纳米技术
化学工程
结晶学
晶体结构
物理化学
化学
催化作用
有机化学
吸附
冶金
复合材料
工程类
作者
Jiali Fu,Qingxue Hui,Yu Gu,Qi Ding,Hongxia Xu,Biao Yang,Chengyu Huangfu,Q.D. Wang,Xinli Liu,Xin‐Yi Wang,Youting Wu,Xingbang Hu,Shuai Yuan,Zhaoqiang Zhang
标识
DOI:10.1002/anie.202514417
摘要
Abstract Separation of C 2 H 2 from industrially important gas pairs using energy‐efficient adsorptive techniques with multifunctional porous materials remains a significant yet challenging issue. Here, we report the highly efficient separation of C 2 H 2 /CO 2 and C 2 H 2 /C 2 H 4 mixtures with isostructural metal‐containing hydrogen‐bonded organic frameworks (M–HOFs), which feature micropore channels decorated with high‐density and uncoordinated carboxyl groups. Single‐crystal X‐ray diffraction analysis reveals that each free carboxyl group is capable of trapping one C 2 H 2 molecule through hydrogen bonding. This endows the M–HOFs with excellent C 2 H 2 capture capability, achieving a benchmark storage density of 396.0 mg cm −3 , while simultaneously demonstrating remarkable selectivity over C 2 H 4 (420–97) and CO 2 (188–53). Breakthrough experiments confirm that binary gas mixtures can be efficiently separated by M–HOFs, where an impressive C 2 H 4 productivity (137.4 mol kg −1 ) is realized in the separation of C 2 H 2 /C 2 H 4 (1/99), and an outstanding separation factor (17) is achieved for C 2 H 2 /CO 2 (50/50) splitting. Coupled with their superior chemical stability, these M–HOFs display tremendous potential for practical applications.
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