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Carbon Nitride Photocatalysts with Integrated Oxidation and Reduction Atomic Active Centers for Improved CO2 Conversion.
Ou, Honghui; Ning, Shangbo; Zhu, Peng; Chen, Shenghua; Han, Ali; Kang, Qing; Hu, Zhuofeng; Ye, Jinhua; Wang, Dingsheng; Li, Yadong.
Afiliación
  • Ou H; Department of Chemistry, Tsinghua University, Beijing, 100084, P. R. China.
  • Ning S; TJU-NIMS International Collaboration Laboratory, School of Materials Science and Engineering, Tianjin University, Tianjin, 300072, P. R. China.
  • Zhu P; Department Institute of Surface Analysis and Chemical Biology, University of Jinan, Jinan, Shandong 250022, P. R. China.
  • Chen S; Department of Chemistry, Tsinghua University, Beijing, 100084, P. R. China.
  • Han A; Department of Chemistry, Tsinghua University, Beijing, 100084, P. R. China.
  • Kang Q; Department of Chemistry, Tsinghua University, Beijing, 100084, P. R. China.
  • Hu Z; Department Institute of Surface Analysis and Chemical Biology, University of Jinan, Jinan, Shandong 250022, P. R. China.
  • Ye J; Guangdong Provincial Key Laboratory of Environmental Pollution Control and Remediation Technology, School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou, 510006, P. R. China.
  • Wang D; TJU-NIMS International Collaboration Laboratory, School of Materials Science and Engineering, Tianjin University, Tianjin, 300072, P. R. China.
  • Li Y; International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), Tsukuba, 305-0047, Japan.
Angew Chem Int Ed Engl ; 61(34): e202206579, 2022 Aug 22.
Article en En | MEDLINE | ID: mdl-35715933
ABSTRACT
Single-atom active-site catalysts have attracted significant attention in the field of photocatalytic CO2 conversion. However, designing active sites for CO2 reduction and H2 O oxidation simultaneously on a photocatalyst and combining the corresponding half-reaction in a photocatalytic system is still difficult. Here, we synthesized a bimetallic single-atom active-site photocatalyst with two compatible active centers of Mn and Co on carbon nitride (Mn1 Co1 /CN). Our experimental results and density functional theory calculations showed that the active center of Mn promotes H2 O oxidation by accumulating photogenerated holes. In addition, the active center of Co promotes CO2 activation by increasing the bond length and bond angle of CO2 molecules. Benefiting from the synergistic effect of the atomic active centers, the synthesized Mn1 Co1 /CN exhibited a CO production rate of 47 µmol g-1 h-1 , which is significantly higher than that of the corresponding single-metal active-site photocatalyst.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2022 Tipo del documento: Article