Enhanced conversion of CO2 into C2H4 on single atom Cu-anchored graphitic carbon nitride: Synergistic diatomic active sites interaction

Abstract

Single atom metal–nitrogen–carbon materials have emerged as remarkably potent catalysts, demonstrating unprecedented potential for the photo-driven reduction of CO2. Herein, a unique Cu@g-C3N5 catalyst obtained by cooperation of single atom Cu and nitrogen-rich g-C3N5 is proposed. The particular CuN diatomic active sites (DAS) in Cu@g-C3N5 contribute to the formation of highly stable CuOCN adsorption, a key configuration for CO2 activation and CC coupling. The synergistic diatomic active sites interaction is found responsible for the efficient photoreduction of CO2 to C2H4 which has been demonstrated in our Gibbs free energy calculation and COHP analysis. The CO2 activation mechanism was studied, the charge density difference and DOS analysis show that the low oxidation state Cu atom significantly affects the electronic structure of g-C3N5 and then enhance the catalytic activity of CO2 hydrogenation.