Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water Oxidation

Abstract Bismuth vanadate (BiVO4) is known as one of the most potential candidates in photocatalytic water oxidation for supplying oxygen in extreme environment. However, its photocatalytic oxygen evolution is hindered by the rapid photogenerated charge carrier separation efficiency. Herein, plasmon...

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Main Authors: Liyang Li, Zhiming Chen, Dong Fang, Jingxiang Low, Jianhong Yi
Format: Article
Language:English
Published: Wiley 2025-08-01
Series:Advanced Science
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Online Access:https://doi.org/10.1002/advs.202500666
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author Liyang Li
Zhiming Chen
Dong Fang
Jingxiang Low
Jianhong Yi
author_facet Liyang Li
Zhiming Chen
Dong Fang
Jingxiang Low
Jianhong Yi
author_sort Liyang Li
collection DOAJ
description Abstract Bismuth vanadate (BiVO4) is known as one of the most potential candidates in photocatalytic water oxidation for supplying oxygen in extreme environment. However, its photocatalytic oxygen evolution is hindered by the rapid photogenerated charge carrier separation efficiency. Herein, plasmonic bismuth (Bi) nanoparticles loaded BiVO4 is prepared for photocatalytic water oxidation. Specifically, the plasmonic bismuth nanoparticles are in situ loaded on the BiVO4 via reduction of partial BiVO4, allowing the formation of the Bi─O─V covalent bridges. Based on the femtosecond transient absorption spectroscopy and density functional theory calculations, such Bi─O─V covalent bridges can significantly facilitate the migration of the plasmonic‐induced hot electrons from Bi to BiVO4, allowing more photogenerated charge carrier to participate in the surface reaction. As a result, the optimized Bi/BiVO4 demonstrates a record‐high photocatalytic evolution rate of 4567.94 µmol h−1 g−1. More importantly, the obtained Bi/BiVO4 show plausible photocatalytic water oxidation capability (oxygen production rate of 381.47 µmol h−1 g−1) under near‐infrared light irradiation, further collaborating its potential to be utilized in extreme conditions. This work on design of low‐cost and highly‐efficient photocatalysts for water oxidation is anticipated to push forward the development of photocatalytic oxygen production in various application scenarios.
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publishDate 2025-08-01
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spelling doaj-art-614245aefb0741a6814d5dbb8e7bf22a2025-08-23T14:14:30ZengWileyAdvanced Science2198-38442025-08-011231n/an/a10.1002/advs.202500666Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water OxidationLiyang Li0Zhiming Chen1Dong Fang2Jingxiang Low3Jianhong Yi4Faculty of Materials Science and Engineering Kunming University of Science and Technology Kunming 650093 P. R. ChinaSchool of Physical Science and Technology Tiangong University Tianjin 300387 P. R. ChinaFaculty of Materials Science and Engineering Kunming University of Science and Technology Kunming 650093 P. R. ChinaSchool of Physical Science and Technology Tiangong University Tianjin 300387 P. R. ChinaFaculty of Materials Science and Engineering Kunming University of Science and Technology Kunming 650093 P. R. ChinaAbstract Bismuth vanadate (BiVO4) is known as one of the most potential candidates in photocatalytic water oxidation for supplying oxygen in extreme environment. However, its photocatalytic oxygen evolution is hindered by the rapid photogenerated charge carrier separation efficiency. Herein, plasmonic bismuth (Bi) nanoparticles loaded BiVO4 is prepared for photocatalytic water oxidation. Specifically, the plasmonic bismuth nanoparticles are in situ loaded on the BiVO4 via reduction of partial BiVO4, allowing the formation of the Bi─O─V covalent bridges. Based on the femtosecond transient absorption spectroscopy and density functional theory calculations, such Bi─O─V covalent bridges can significantly facilitate the migration of the plasmonic‐induced hot electrons from Bi to BiVO4, allowing more photogenerated charge carrier to participate in the surface reaction. As a result, the optimized Bi/BiVO4 demonstrates a record‐high photocatalytic evolution rate of 4567.94 µmol h−1 g−1. More importantly, the obtained Bi/BiVO4 show plausible photocatalytic water oxidation capability (oxygen production rate of 381.47 µmol h−1 g−1) under near‐infrared light irradiation, further collaborating its potential to be utilized in extreme conditions. This work on design of low‐cost and highly‐efficient photocatalysts for water oxidation is anticipated to push forward the development of photocatalytic oxygen production in various application scenarios.https://doi.org/10.1002/advs.202500666BiVO4covalent bridgeelectron transferheterojunctionphotocatalysis
spellingShingle Liyang Li
Zhiming Chen
Dong Fang
Jingxiang Low
Jianhong Yi
Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water Oxidation
Advanced Science
BiVO4
covalent bridge
electron transfer
heterojunction
photocatalysis
title Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water Oxidation
title_full Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water Oxidation
title_fullStr Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water Oxidation
title_full_unstemmed Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water Oxidation
title_short Covalent Bridges in Bi Loaded BiVO4 Enabling Rapid Charge Transfer for Efficient Photocatalytic Water Oxidation
title_sort covalent bridges in bi loaded bivo4 enabling rapid charge transfer for efficient photocatalytic water oxidation
topic BiVO4
covalent bridge
electron transfer
heterojunction
photocatalysis
url https://doi.org/10.1002/advs.202500666
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AT zhimingchen covalentbridgesinbiloadedbivo4enablingrapidchargetransferforefficientphotocatalyticwateroxidation
AT dongfang covalentbridgesinbiloadedbivo4enablingrapidchargetransferforefficientphotocatalyticwateroxidation
AT jingxianglow covalentbridgesinbiloadedbivo4enablingrapidchargetransferforefficientphotocatalyticwateroxidation
AT jianhongyi covalentbridgesinbiloadedbivo4enablingrapidchargetransferforefficientphotocatalyticwateroxidation