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- W2091639403 abstract "A metal–organic framework (MOF)-based catalyst W–Cu–BTC is designed by hybridizing highly active W ions into Cu3(BTC)2(H2O)3 (also known as Cu–BTC or HKUST-1, BTC = 1,3,5-tricarboxylate benzene) frameworks based on density functional (DFT) calculations. We show that the hybrid W–Cu node plays a pivotal role in activating CO2 according to frontier molecular orbital theory. In contrast to the Lewis-acid nature of open metal sites in most MOFs, the exposed W ion in W–Cu–BTC is identified as a Lewis-base site, evidenced by the substantial electron donation from W ion to CO2. Kinetically, the linear CO2 molecule can be readily bent by forming a CO2–W complex after overcoming a negligible activation barrier of 0.09 eV. In addition, we present calculated infrared spectra (IR) and X-Ray spectra (XPS) for reference in future experimental studies." @default.
- W2091639403 created "2016-06-24" @default.
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- W2091639403 date "2012-01-01" @default.
- W2091639403 modified "2023-10-03" @default.
- W2091639403 title "Catalyzed activation of CO2 by a Lewis-base site in W–Cu–BTC hybrid metal organic frameworks" @default.
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- W2091639403 doi "https://doi.org/10.1039/c2sc20521a" @default.
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