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Fe-Based MOFs for Photocatalytic CO2 Reduction: Role of Coordination Unsaturated Sites and Dual Excitation Pathways

Wang, Dengke, Huang, Renkun, Liu, Wenjun, Sun, Dengrong, Li, Zhaohui·2014·ACS Catalysis

Abstract

The utilization of solar energy for the conversion of CO 2 into valuable organic products is one of the best solutions to solve the problems of global warming and energy shortage. The development of photocatalysts capable of reducing CO 2 under visible light, especially those containing earth-abundant metals, is significant. Herein we report that a series of earth-abundant Fe-containing MOFs (MIL-101(Fe), MIL-53(Fe), MIL-88B(Fe)) show photocatalytic activity for CO 2 reduction to give formate under visible light irradiation. The direct excitation of the Fe–O clusters in these MOFs induces the electron transfer from O 2– to Fe 3+ to form Fe 2+, which is responsible for the photocatalytic CO 2 reduction. Among the three investigated Fe-based MOFs, MIL-101(Fe) showed the best activity due to the existence of the coordination unsaturated Fe sites in its structure. All three amine-functionalized Fe-containing MOFs (NH 2 -MIL-101(Fe), NH 2 -MIL-53(Fe) and NH 2 -MIL-88B(Fe)) showed enhanced photocatalytic activity in comparison to the unfunctionalized MOF, due to the existence of dual excitation pathways: i.e., excitation of an NH 2 functionality followed by an electron transfer to the Fe center in addition to the direct excitation of Fe–O clusters.

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Metadata

Authors
Wang, D., Huang, R., Liu, W., Sun, D., & Li, Z.
Venue
ACS Catalysis
Published
2014-10-31
Volume
4
Issue
12
Pages
4254-4260
ISSN
2155-5435 (ISSN-L)
OpenAlex
W2322118693
Cited by
869
References
2
FWCI
13.86
Type
journal article
Language
en
Open access
closed

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