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

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.

CO2 reduction with Re(i)-NHC compounds: driving selective catalysis with a silicon nanowire photoelectrode.

The CO2-reduction activity of two Re(i)-NHC complexes is investigated employing a silicon nanowire photoelectrode to drive catalysis. Photovoltages greater than 440 mV are observed along with excellent selectivity towards CO over H2 formation. The observed selectivity towards CO production correlates with strong adsorption of the catalysts on the photoelectrode surface.