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
气体分离
俘获
多孔介质
纳米技术
多孔性
化学工程
精细化工
水准点(测量)
分离(统计)
密度泛函理论
有机分子
二进制数
氢分子
特征(语言学)
衍射
选择性吸附
化学
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
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-30
卷期号:64 (48): e202514417-e202514417
被引量:6
标识
DOI:10.1002/anie.202514417
摘要
Separation of C2H2 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 C2H2/CO2 and C2H2/C2H4 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 C2H2 molecule through hydrogen bonding. This endows the M-HOFs with excellent C2H2 capture capability, achieving a benchmark storage density of 396.0 mg cm-3, while simultaneously demonstrating remarkable selectivity over C2H4 (420-97) and CO2 (188-53). Breakthrough experiments confirm that binary gas mixtures can be efficiently separated by M-HOFs, where an impressive C2H4 productivity (137.4 mol kg-1) is realized in the separation of C2H2/C2H4 (1/99), and an outstanding separation factor (17) is achieved for C2H2/CO2 (50/50) splitting. Coupled with their superior chemical stability, these M-HOFs display tremendous potential for practical applications.
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