An ultra-tunable platform for molecular engineering of high-performance crystalline porous materials

Metal-organic frameworks are a class of crystalline porous materials with potential applications in catalysis, gas separation and storage, and so on. Of great importance is the development of innovative synthetic strategies to optimize porosity, composition and functionality to target specific appli...

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Published inNature communications Vol. 7; no. 1; p. 13645
Main Authors Zhai, Quan-Guo, Bu, Xianhui, Mao, Chengyu, Zhao, Xiang, Daemen, Luke, Cheng, Yongqiang, Ramirez-Cuesta, Anibal J., Feng, Pingyun
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 07.12.2016
Nature Publishing Group
Nature Portfolio
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Summary:Metal-organic frameworks are a class of crystalline porous materials with potential applications in catalysis, gas separation and storage, and so on. Of great importance is the development of innovative synthetic strategies to optimize porosity, composition and functionality to target specific applications. Here we show a platform for the development of metal-organic materials and control of their gas sorption properties. This platform can accommodate a large variety of organic ligands and homo- or hetero-metallic clusters, which allows for extraordinary tunability in gas sorption properties. Even without any strong binding sites, most members of this platform exhibit high gas uptake capacity. The high capacity is accomplished with an isosteric heat of adsorption as low as 20 kJ mol −1 for carbon dioxide, which could bring a distinct economic advantage because of the significantly reduced energy consumption for activation and regeneration of adsorbents. Synthetic design of crystalline porous materials is important for applications such as catalysis and adsorption. Here, the authors demonstrate a platform for the development of crystalline porous materials with a variety of organic ligands and metallic clusters, and control of their gas sorption properties.
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USDOE
AC05-00OR22725
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms13645