Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 15, Pages 8455-8459Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202015735
Keywords
carbon dioxide fixation; charge transfer; metal– organic frameworks; nanostructures; photosynthesis
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Funding
- Hong Kong Research Grant Council (RGC) General Research Fund [CityU 11305419]
- Australian Research Council Discovery Project [DP180102540]
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Encapsulating Cu2O nanowires in metal-organic frameworks (MOFs) enhances activity and stability, facilitates charge separation and CO2 uptake, leading to selective photocatalytic CO2 reduction into CH4. This work demonstrates an effective strategy for CO2 conversion by integrating MOFs with metal oxide photocatalyst.
Improving the stability of cuprous oxide (Cu2O) is imperative to its practical applications in artificial photosynthesis. In this work, Cu2O nanowires are encapsulated by metal-organic frameworks (MOFs) of Cu-3(BTC)(2) (BTC=1,3,5-benzene tricarboxylate) using a surfactant-free method. Such MOFs not only suppress the water vapor-induced corrosion of Cu2O but also facilitate charge separation and CO2 uptake, thus resulting in a nanocomposite representing 1.9 times improved activity and stability for selective photocatalytic CO2 reduction into CH4 under mild reaction conditions. Furthermore, direct transfer of photogenerated electrons from the conduction band of Cu2O to the LUMO level of non-excited Cu-3(BTC)(2) has been evidenced by time-resolved photoluminescence. This work proposes an effective strategy for CO2 conversion by a synergy of charge separation and CO2 adsorption, leading to the enhanced photocatalytic reaction when MOFs are integrated with metal oxide photocatalyst.
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