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

  • Peipei Huang
  • , Jiahao Huang
  • , Sebastian A. Pantovich
  • , Alexander D. Carl
  • , Thomas G. Fenton
  • , Christine A. Caputo
  • , Ronald L. Grimm
  • , Anatoly I. Frenkel
  • , Gonghu Li
  • University of New Hampshire
  • Stony Brook University
  • Worcester Polytechnic Institute

Research output: Contribution to journalArticlepeer-review

373 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)16042-16047
Number of pages6
JournalJournal of the American Chemical Society
Volume140
Issue number47
DOIs
StatePublished - Nov 28 2018

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