金属
无机化学
离子键合
溶解度
水溶液中的金属离子
化学
作者
Vahid Nozari,Courtney Calahoo,Joshua M. Tuffnell,David A. Keen,Thomas D. Bennett,Lothar Wondraczek
标识
DOI:10.1038/s41467-021-25970-0
摘要
Hybrid glasses from melt-quenched metal-organic frameworks (MOFs) have been emerging as a new class of materials, which combine the functional properties of crystalline MOFs with the processability of glasses. However, only a handful of the crystalline MOFs are meltable. Porosity and metal-linker interaction strength have both been identified as crucial parameters in the trade-off between thermal decomposition of the organic linker and, more desirably, melting. For example, the inability of the prototypical zeolitic imidazolate framework (ZIF) ZIF-8 to melt, is ascribed to the instability of the organic linker upon dissociation from the metal center. Here, we demonstrate that the incorporation of an ionic liquid (IL) into the porous interior of ZIF-8 provides a means to reduce its melting temperature to below its thermal decomposition temperature. Our structural studies show that the prevention of decomposition, and successful melting, is due to the IL interactions stabilizing the rapidly dissociating ZIF-8 linkers upon heating. This understanding may act as a general guide for extending the range of meltable MOF materials and, hence, the chemical and structural variety of MOF-derived glasses. The variety of hybrid glasses from metal-organic frameworks (MOFs) has remained strongly limited to only a handful of compounds. Here, the authors introduce a route to melt highly porous and non-meltable MOFs using ionic liquids in order to extend the range of MOF glasses.
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