分子间力
膜
气体分离
氢键
材料科学
分子
金属有机骨架
共价键
纳米技术
非共价相互作用
多孔性
选择性
化学工程
化学物理
化学
物理化学
有机化学
吸附
催化作用
复合材料
工程类
生物化学
作者
Hao Zhan,Tianxiang Yang,Wenyu Xiang,Xiang‐Kui Ren,Zhi Wang,Song Zhao
出处
期刊:Small
[Wiley]
日期:2025-06-10
被引量:1
标识
DOI:10.1002/smll.202504508
摘要
As an emerging class of porous solid materials, metal-organic polyhedra (MOPs), possess inherent porosity and excellent solvent processability, making them highly promising candidates for membrane separation applications. However, the development of continuous and structurally stable MOP-based membranes remains a significant challenge due to the weak noncovalent intermolecular interactions. Herein, an intermolecular transitions strategy is implemented to enhance the intermolecular interactions within MOPs molecules. By transforming unstable intermolecular hydrogen bonds into stable covalent bonds, the continuous metal-organic polyhedral (cMOP) film is successfully constructed. The robust channel-guest interaction between the angstrom-scale channels and CO2 molecules endows the prepared cMOP composite membrane with a remarkable CO2/N2 selectivity of 38 at 1 bar, underscoring the feasibility of employing MOPs to construct efficient continuous angstrom-scale channels for precise gas separation. These findings offer valuable theoretical insights into the continuous assembly of metal-organic porous materials, which is promising for the fabrication of membranes for efficient gas separations.
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