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Regulating the Transfer of Photogenerated Carriers for Photocatalytic Hydrogen Evolution Coupled with Furfural Synthesis.
Liu, Boxin; Li, Yanfang; Guo, Yuchen; Tang, Yuan; Wang, Chunyang; Sun, Yan; Tan, Xin; Hu, Zhuofeng; Yu, Tao.
Affiliation
  • Liu B; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, P. R. China.
  • Li Y; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, P. R. China.
  • Guo Y; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, P. R. China.
  • Tang Y; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, P. R. China.
  • Wang C; School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, P. R. China.
  • Sun Y; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, P. R. China.
  • Tan X; School of Environmental Science and Engineering, Tianjin University, Tianjin 300350, P. R. China.
  • Hu Z; School of Environmental Science and Engineering, Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, Sun Yat-sen University, Guangzhou 510006, P. R. China.
  • Yu T; School of Chemical Engineering and Technology, Tianjin University, Tianjin 300350, P. R. China.
ACS Nano ; 18(27): 17939-17949, 2024 Jul 09.
Article in En | MEDLINE | ID: mdl-38918079
ABSTRACT
How to simultaneously utilize photogenerated electrons and holes still remains a critical challenge in the field of artificial photosynthesis, especially in the process of photocatalytic hydrogen (H2) evolution coupled with biomass oxidation to value-added chemicals. Herein, a series-parallel photocatalyst (Cu NPs/CdS/In2O3) that can intrinsically regulate the transfer of photogenerated carriers is ingeniously designed for photocatalytic H2 evolution synergized with furfural alcohol (FFA) selective oxidation to furfural (FF). Accordingly, the desired H2 and FF evolution rates with near 100% selectivity toward FF are achieved on Cu NPs/CdS/In2O3 in a sealed atmospheric system. Experimental and theoretical analyses confirm that the localized surface plasmon resonance (LSPR) effect induced by Cu NPs accelerates the reduction of protons (H+) to H2 efficiently, while the photogenerated holes from In2O3 preferentially activate the α-C-H bond of FFA adsorbed on Lewis acid sites to generate FF. This work provides a reference for regulating the transfer of photogenerated carriers for H2 evolution coupled with FF synthesis.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ACS Nano Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: ACS Nano Year: 2024 Document type: Article