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Photocatalytic Generation of H2O2 Via a Hydrogen-Abstraction Pathway by Bi2.15WO6 under Visible Light.
Ren, Hai-Tao; Cai, Chao-Chen; Zhu, Peng-Yue; Wang, Cong; Wu, Song-Hai; Liu, Yong; Han, Xu.
  • Ren HT; Tianjin and Ministry of Education Key Laboratory of Advanced Textile Composite Materials, School of Textile Science and Engineering, Tiangong University, Tianjin 300387, P.R. China.
  • Cai CC; Tianjin and Ministry of Education Key Laboratory of Advanced Textile Composite Materials, School of Textile Science and Engineering, Tiangong University, Tianjin 300387, P.R. China.
  • Zhu PY; School of Environmental Science and Engineering, Tianjin University, Tianjin 300072, P.R. China.
  • Wang C; Hebei Key Laboratory of Hazardous Chemicals Safety and Control Technology, School of Chemical Safety, North China Institute of Science and Technology, Langfang Hebei 065201, P.R. China.
  • Wu SH; School of Chemical Engineering and Technology, Tianjin University, Tianjin 300382, P.R. China.
  • Liu Y; School of Chemistry and Chemical Engineering, Tianjin University of Technology, Tianjin 300382, P.R. China.
  • Han X; School of Chemical Engineering and Technology, Tianjin University, Tianjin 300382, P.R. China.
Langmuir ; 40(14): 7384-7394, 2024 Apr 09.
Article en En | MEDLINE | ID: mdl-38530344
ABSTRACT
Photocatalytic technology is a popular research area for converting solar energy into environmentally friendly chemicals and is considered the greenest approach for producing H2O2. However, the corresponding reactive oxygen species (ROS) and pathway involved in the photocatalytic generation of H2O2 by the Bi2.15WO6-glucose system are still not clear. Quenching experiments have established that neither •OH nor h+ contribute to the formation of H2O2, and show that the formed surface superoxo (≡Bi-OO•) and peroxo (≡Bi-OOH) species are the predominant ROS in H2O2 generation. In addition, various characterizations indicate the enhanced electron-transfer on the surface of Bi2.15WO6 with increasing contents of glucose via the ligand-to-metal charge transfer pathway, confirming H-transfer from glucose to ≡Bi-OO• or ≡Bi-OOH. The increased production of H2O2 with decreasing bond dissociation energy (BDEO-H) values of various phenolic compounds again supports the H-transfer mechanism from phenolic compounds to ≡Bi-OO• and then to ≡Bi-OOH. DFT calculations further reveal that on the Bi2.15WO6 surface, oxygen is sequentially reduced to ≡Bi-OO• and ≡Bi-OOH, while H-transfer from H2O or glucose to ≡Bi-OO• and ≡Bi-OOH, resulting in the production of H2O2. The lower energy barrier of H-transfer from adsorbed glucose (0.636 eV) than that from H2O (1.157 eV) indicates that H-transfer is more favorable from adsorbed glucose. This work gives new insight into the photocatalytic generation of H2O2 by Bi2.15WO6 in the presence of glucose/phenolic compounds via the H-abstraction pathway.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article