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WO3/BiOBr S-Scheme Heterojunction Photocatalyst for Enhanced Photocatalytic CO2 Reduction.
Li, Chen; Lu, Xingyu; Chen, Liuyun; Xie, Xinling; Qin, Zuzeng; Ji, Hongbing; Su, Tongming.
Afiliação
  • Li C; Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
  • Lu X; Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
  • Chen L; Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
  • Xie X; Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
  • Qin Z; Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
  • Ji H; Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, China.
  • Su T; State Key Laboratory Breeding Base of Green-Chemical Synthesis Technology, Institute of Green Petroleum Processing and Light Hydrocarbon Conversion, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014, China.
Materials (Basel) ; 17(13)2024 Jun 30.
Article em En | MEDLINE | ID: mdl-38998282
ABSTRACT
The photocatalytic CO2 reduction strategy driven by visible light is a practical way to solve the energy crisis. However, limited by the fast recombination of photogenerated electrons and holes in photocatalysts, photocatalytic efficiency is still low. Herein, a WO3/BiOBr S-scheme heterojunction was formed by combining WO3 with BiOBr, which facilitated the transfer and separation of photoinduced electrons and holes and enhanced the photocatalytic CO2 reaction. The optimized WO3/BiOBr heterostructures exhibited best activity for photocatalytic CO2 reduction without any sacrificial reagents, and the CO yield reached 17.14 µmol g-1 after reaction for 4 h, which was 1.56 times greater than that of BiOBr. The photocatalytic stability of WO3/BiOBr was also improved.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article