选择性
吸附
吸附
表面电荷
表面改性
多孔性
调制(音乐)
静电学
选择性吸附
材料科学
金属有机骨架
静电相互作用
化学工程
纳米技术
化学物理
化学
有机化学
物理化学
催化作用
哲学
美学
工程类
作者
Salamanti Ainiwaner,Hengcong Huang,Jia-Jia Zheng,Fengting Li,Xue-Tong Yang,Yangyang Guo,Fangli Yuan,Ming‐Shui Yao,Yifan Gu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-08-20
卷期号:17 (11): 10083-10087
被引量:23
标识
DOI:10.1007/s12274-024-6883-z
摘要
The regulation of gas sorption via simple pore modification is crucial to molecular recognition and chemical separation. Herein, a rational pore surface electrostatic modulation in synthetic one dimensioned (1-D) channel is demonstrated to boost ethane/ethylene (C2H6/C2H4) selectivity for one-step extraction of C2H4 from C2H6/C2H4 mixtures. Through the precise modulation of the surface charge arrangement with negatively charged moieties in the 1-D channel of a metal—organic framework (MOF), enhanced C2H6—host framework and decreased C2H4—host framework electrostatic interactions were obtained, which resulted in an obvious improvement in adsorption selectivity. Furthermore, the breakthrough separation performance rendered the obtained MOF an efficient adsorbent for C2H4 purification from C2H6/C2H4 mixture. The combined detail theoretical studies prove that the gas sorption selectivity is remarkably sensitive to framework electrostatic change even in the case of pore surface modification at the atomic level. These results are of fundamental importance to the design of porous materials for challenging separation tasks.
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