化学
选择性
连接器
吸附
极地的
极性(国际关系)
化学极性
极化率
选择性吸附
工作(物理)
氯
分子
组合化学
分子动力学
化学工程
计算化学
调制(音乐)
分子识别
亲缘关系
位阻效应
单层
纳米技术
无机化学
化学物理
作者
Hui‐Fang Ma,Yue Wang,Junmin Chen,Hui‐Ping Xiao,Wen-Rou Yu,Qing‐Yan Liu
标识
DOI:10.1021/acs.inorgchem.6c04424
摘要
Abstract Efficient separation of Xe/Kr mixture remains a challenge, due to their chemical inertness and the striking similarity of their physicochemical properties. In this work, the chlorine-decorated metal–organic framework (MOF) of JXNU-24(Cl) and its pristine JXNU-24 are presented for Xe/Kr separation. The chlorine-functionalized framework with a more polar pore microenvironment exhibits a stronger binding affinity toward Xe. Consequently, JXNU-24(Cl) exhibits a Xe/Kr adsorption selectivity of 10.3 and outstanding separation performance with a high productivity of 184 L kg–1 for high-purity Kr (>99.9%). Computational simulations reveal that the presence of chlorine substituents generates polar pore surfaces, which preferentially interact with the more polarizable Xe molecules, thereby enhancing Xe-framework interactions and Xe/Kr selectivity for JXNU-24(Cl). This work achieves preferential Xe recognition via framework polarity modulation and offers an effective molecular design strategy for constructing MOFs for efficient Xe/Kr separation.
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