| Literature DB >> 27736031 |
Huabin Zhang1, Jing Wei2, Juncai Dong3, Guigao Liu1, Li Shi1, Pengfei An3, Guixia Zhao1, Jintao Kong2, Xiaojun Wang1, Xianguang Meng1, Jing Zhang3, Jinhua Ye4,5,6.
Abstract
Modular optimization of metal-organic frameworks (MOFs) was realized by incorporation of coordinatively unsaturated single atoms in a MOF matrix. The newly developed MOF can selectively capture and photoreduce CO2 with high efficiency under visible-light irradiation. Mechanistic investigation reveals that the presence of single Co atoms in the MOF can greatly boost the electron-hole separation efficiency in porphyrin units. Directional migration of photogenerated excitons from porphyrin to catalytic Co centers was witnessed, thereby achieving supply of long-lived electrons for the reduction of CO2 molecules adsorbed on Co centers. As a direct result, porphyrin MOF comprising atomically dispersed catalytic centers exhibits significantly enhanced photocatalytic conversion of CO2 , which is equivalent to a 3.13-fold improvement in CO evolution rate (200.6 μmol g-1 h-1 ) and a 5.93-fold enhancement in CH4 generation rate (36.67 μmol g-1 h-1 ) compared to the parent MOF.Entities:
Keywords: CO2 reduction; active sites; heterogeneous catalysis; photocatalysis; solar-energy conversion
Year: 2016 PMID: 27736031 DOI: 10.1002/anie.201608597
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336