{"title":"Vacancy-engineered bismuth vanadate for photoelectrocatalytic glycerol oxidation with simultaneous hydrogen production†","authors":"Haoyue Sun, Rui Tang, Lizhuo Wang, Yuhang Liang, Wenjie Yang, Zhisheng Lin, Xingmo Zhang, Kaijuan Chen, Weibin Liang, Shenlong Zhao, Rongkun Zheng and Jun Huang","doi":"10.1039/D4EY00211C","DOIUrl":null,"url":null,"abstract":"<p >Photoelectrocatalytic (PEC) water splitting offers a sustainable pathway for clean H<small><sub>2</sub></small> production, and its integration with biomass valorization further enhances eco-economic efficiency. In this study, a BiVO<small><sub>4</sub></small> catalyst with an optimized oxygen vacancy (Ov-BVO) concentration was grown on a SnO<small><sub>2</sub></small> skeleton, achieving efficient PEC glycerol oxidation to selectively produce dihydroxyacetone (DHA) and H<small><sub>2</sub></small> under neutral conditions. By incorporating Ov-BVO with SnO<small><sub>2</sub></small>, the light-harvesting and photo-induced carrier transfer efficiencies were significantly improved. Ov played a crucial role in selectively absorbing and activating the secondary –OH group of glycerol molecules, as revealed by theoretical and experimental studies. However, excessive Ov induced carrier recombination, underscoring the need for an optimal Ov concentration, which was achieved by tailoring heat treatment conditions. The SnO<small><sub>2</sub></small>/BVO-400 catalyst demonstrated a trade-off between the prolonged carrier lifetime and efficient reactant adsorption, exhibiting a PEC DHA productivity of 144 mmol m<small><sup>−2</sup></small> h<small><sup>−1</sup></small> with 26.5% selectivity, alongside H<small><sub>2</sub></small> generation (1850 mmol m<small><sup>−2</sup></small> h<small><sup>−1</sup></small>). This work lays the groundwork to achieve value-added chemical fabrication through neutral PEC glycerol reforming and the potential scale-up of this sustainable technology.</p>","PeriodicalId":72877,"journal":{"name":"EES catalysis","volume":" 2","pages":" 337-346"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ey/d4ey00211c?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EES catalysis","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ey/d4ey00211c","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Photoelectrocatalytic (PEC) water splitting offers a sustainable pathway for clean H2 production, and its integration with biomass valorization further enhances eco-economic efficiency. In this study, a BiVO4 catalyst with an optimized oxygen vacancy (Ov-BVO) concentration was grown on a SnO2 skeleton, achieving efficient PEC glycerol oxidation to selectively produce dihydroxyacetone (DHA) and H2 under neutral conditions. By incorporating Ov-BVO with SnO2, the light-harvesting and photo-induced carrier transfer efficiencies were significantly improved. Ov played a crucial role in selectively absorbing and activating the secondary –OH group of glycerol molecules, as revealed by theoretical and experimental studies. However, excessive Ov induced carrier recombination, underscoring the need for an optimal Ov concentration, which was achieved by tailoring heat treatment conditions. The SnO2/BVO-400 catalyst demonstrated a trade-off between the prolonged carrier lifetime and efficient reactant adsorption, exhibiting a PEC DHA productivity of 144 mmol m−2 h−1 with 26.5% selectivity, alongside H2 generation (1850 mmol m−2 h−1). This work lays the groundwork to achieve value-added chemical fabrication through neutral PEC glycerol reforming and the potential scale-up of this sustainable technology.