沸石咪唑盐骨架
吸附
熵(时间箭头)
组态熵
咪唑酯
氢
液化
金属有机骨架
材料科学
化学工程
热力学
化学
物理化学
无机化学
有机化学
物理
工程类
作者
Joohan Nam,Changhyeon Cho,Sungyeop Jung,Minji Jung,Yeong-Jin Kim,Yejin Hong,Sohyeon Lee,Hyunchul Oh,Wonyoung Choe
标识
DOI:10.1002/anie.202420379
摘要
Entropy‐driven strategy enables the systematic design of complex systems by using entropy as a quantifiable design parameter for the degree of mixing. In this study, we present mixed‐linker zeolitic imidazolate frameworks (ZIFs), sod‐ZIF‐1 series, that features two types of six‐membered rings (6MRs) with aperture sizes of 3.4 Å and 1.7 Å. By adjusting the configurational entropy, the ratio of these 6MRs can be systematically controlled, which significantly influences adsorptive properties, particularly improving the H2 affinity about 3 times throughout the series. This results in the significant enhancement of retention times in dynamic separation of hydrogen isotopes (D2/H2), even over LNG liquefaction temperature. This approach to entropy‐driven pore engineering provides new opportunities for enhancing gas adsorption and separation processes.
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