吸附
多孔性
材料科学
吸附
配位几何学
结晶学
协调数
粉末衍射
铜
纳米技术
化学工程
化学物理
化学
离子
分子
复合材料
物理化学
有机化学
冶金
工程类
氢键
作者
Terumasa SHIMADA,Pavel M. Usov,Yuki Wada,Hiroyoshi Ohtsu,Taku Watanabe,Kiyohiro Adachi,Daisuke Hashizume,Takaya Matsumoto,Masaki Kawano
出处
期刊:Advanced Science
[Wiley]
日期:2023-11-20
卷期号:11 (2): e2307417-e2307417
被引量:4
标识
DOI:10.1002/advs.202307417
摘要
Abstract A coordination network containing isolated pores without interconnecting channels is prepared from a tetrahedral ligand and copper(I) iodide. Despite the lack of accessibility, CO 2 is selectively adsorbed into these pores at 298 K and then retained for more than one week while exposed to the atmosphere. The CO 2 adsorption energy and diffusion mechanism throughout the network are simulated using Matlantis, which helps to rationalize the experimental results. CO 2 enters the isolated voids through transient channels, termed “magic doors”, which can momentarily appear within the structure. Once inside the voids, CO 2 remains locked in limiting its escape. This mechanism is facilitated by the flexibility of organic ligands and the pivot motion of cluster units. In situ powder X‐ray diffraction revealed that the crystal structure change is negligible before and after CO 2 capture, unlike gate‐opening coordination networks. The uncovered CO 2 sorption and retention ability paves the way for the design of sorbents based on isolated voids.
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