介孔材料
成核
纳米反应器
微型多孔材料
笼状水合物
水合物
化学工程
材料科学
氢
化学
纳米技术
纳米颗粒
催化作用
有机化学
工程类
作者
Carolina Carrillo‐Carrión,Judit Farrando‐Perez,Luke L. Daemen,Yongqiang Cheng,Anibal J. Ramirez‐Cuesta,Joaquín Silvestre-Alberó
标识
DOI:10.1002/anie.202315280
摘要
Abstract We report the first experimental evidence for rapid formation of hydrogen clathrates under mild pressure and temperature conditions within the cavities of a zirconium‐metalloporphyrin framework, specifically PCN‐222. PCN‐222 has been selected for its 1D mesoporous channels, high water‐stability, and proper hydrophilic behavior. Firstly, we optimize a microwave (MW)‐assisted method for the synthesis of nanosized PCN‐222 particles with precise structure control (exceptional homogeneity in morphology and crystalline phase purity), taking advantage of MW in terms of rapid/homogeneous heating, time and energy savings, as well as potential scalability of the synthetic method. Second, we explore the relevance of the large mesoporous 1D open channels within the PCN‐222 to promote the nucleation and growth of confined hydrogen clathrates. Experimental results show that PCN‐222 drives the nucleation process at a lower pressure than the bulk system (1.35 kbar vs 2 kbar), with fast kinetics (minutes), using pure water, and with a nearly complete water‐to‐hydrate conversion. Unfortunately, PCN‐222 cannot withstand these high pressures, which lead to a significant alteration of the mesoporous structure while the microporous network remains mainly unchanged.
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