journal article Sep 29, 2021

Surface Local Polarization Induced by Bismuth‐Oxygen Vacancy Pairs Tuning Non‐Covalent Interaction for CO2 Photoreduction

View at Publisher Save 10.1002/aenm.202102389
Abstract
AbstractThe inefficient charge separation and lack of active sites have been regarded as the main obstacles limiting the CO2 photoreduction efficiency. It is highly desirable but challenging to create a local polarization field to accelerate charge separation and build reactive sites for CO2 reduction dynamics. Herein, atomic level bismuth‐oxygen vacancy pairs are engineered into Bi24O31Br10 (BOB) atomic layers to create a local polarization field. It facilitates photogenerated electrons to migrate from BOB to vacancy pair sites and favors the activation of CO2 molecules. Simultaneously, it works as reactive sites to tune the non‐covalent interaction of intermediates and optimizes the reaction process. The vacancy pairs tuned surface atomic structures enable the formation of a highly stable Bi−C−O−Bi intermediate state and consecutive Bi−C−O intermediate, thus changing the rate‐determining step from CO* formation to COOH* formation. Benefiting from these features, the VBiO‐BOB delivers a 20.9‐fold CO2 photoreduction activity enhancement relative to highly crystalline BOB in pure water with highly stability. This work provides new insights for the design of a vacancy pair to create local polarization and tune the non‐covalent interaction.
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Cited By
202
ACS Catalysis
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202
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Details
Published
Sep 29, 2021
Vol/Issue
11(41)
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Authors
Funding
National Natural Science Foundation of China Award: 21725102
Key Technologies Research and Development Program Award: 2017YFA0207301
Cite This Article
Jun Di, Chao Chen, Chao Zhu, et al. (2021). Surface Local Polarization Induced by Bismuth‐Oxygen Vacancy Pairs Tuning Non‐Covalent Interaction for CO2 Photoreduction. Advanced Energy Materials, 11(41). https://doi.org/10.1002/aenm.202102389