沸石咪唑盐骨架
咪唑酯
氢同位素
化学
金属有机骨架
氢
纳米技术
材料科学
无机化学
吸附
物理化学
有机化学
作者
Joohan Nam,Changhyeon Cho,Sungyeop Jung,Minji Jung,Yeongjin Kim,Yejin Hong,Sohyeon Lee,Hyunchul Oh,Wonyoung Choe
标识
DOI:10.1002/ange.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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