4.8 Article

Selective CO2 Reduction Catalyzed by Single Cobalt Sites on Carbon Nitride under Visible-Light Irradiation

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 140, Issue 47, Pages 16042-16047

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b10380

Keywords

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Funding

  1. U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences [DE-SC0016417]
  2. U.S. National Science Foundation [CBET-1510810]
  3. U.S. DOE [DE-FG02-03ER15476]
  4. Laboratory Directed Research and Development Program through Brookhaven National Laboratory under U.S. DOE [LDRD 18-047, DE-SC0012704]
  5. DOE Office of Science by Brookhaven National Laboratory [DE-SC0012704]
  6. Synchrotron Catalysis Consortium (U.S. DOE, Office of Basic Energy Sciences) [DE-SC0012335]
  7. Div Of Chem, Bioeng, Env, & Transp Sys [1510810] Funding Source: National Science Foundation

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Framework nitrogen atoms of carbon nitride (C3N4) can coordinate with and activate metal sites for catalysis. In this study, C3N4 was employed to harvest visible light and activate Co2+ sites, without the use of additional ligands, in photochemical CO2 reduction. Photocatalysts containing single Co2+ sites on C3N4 were prepared by a simple deposition method and demonstrated excellent activity and product selectivity toward CO formation. A turnover number of more than 200 was obtained for CO production using the synthesized photocatalyst under visible-light irradiation. Inactive cobalt oxides formed at relatively high cobalt loadings but did not alter product selectivity. Further studies with X-ray absorption spectroscopy confirmed the presence of single Co2+ sites on C3N4 and their important role in achieving selective CO2 reduction.

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