Coordination of Copper within a Crystalline Carbon Nitride and its Catalytic Reduction of CO₂

Inherently disordered structures of carbon nitrides have hindered an atomic level tunability and understanding of their catalytic reactivity. Starting from a crystalline carbon nitride, poly(triazine imide) or PTI, the coordination of copper cations to its intralayer N-triazine groups was investigated using molten salt reactions. The reaction of PTI/LiCl within CuCl or mixed KCl/CuCl₂ molten salts at 280 to 450 °C could be used to yield three partially disordered and ordered structures, wherein the Cu cations are found to coordinate within its intralayer cavities. Local structural differences and the copper content, i.e., whether full or partial occupancy of the intralayer cavity occurs, were found to be dependent on the reaction temperature and Cu-containing salt. Crystallites of Cu-coordinated PTI were also found to electrophoretically deposit from aqueous particle suspensions onto either graphite or FTO electrodes. As a result, electrocatalytic current densities for the reduction of CO₂ and H₂O reached as high as ~10 to 50 mA/cm², and which remained stable for > 2 days. Selectivity for the reduction of CO₂ to CO vs H₂ increases for thinner crystals as well as for when two Cu cations coordinate within an intralayer cavity of PTI. Mechanistic calculations have also revealed the electrocatalytic activity for CO₂ reduction requires a smaller thermodynamic driving force with two neighboring intralayer Cu atoms as compared to a single intralayer Cu atom. These results establish a useful synthetic pathway to metal-coordination in a crystalline carbon nitride and showing great potential for uses in mediating stable CO₂ reduction at sizable current densities.

Pauly, M.; Deegbey, M.; Keller, L.; McGuigan, S.; Dianat, G.; Wong, J. C.; Murphy, C. G. F.; Shang, B.; Wang, H.; Cahoon, J. F.; Sampaio, R.; Kanai, Y.; Parsons, G.; Jakubikova, E.; Maggard, P. A. Coordination of Copper within a Crystalline Carbon Nitride and its Catalytic Reduction of CO₂, Dalton Trans., 2024, 53, 6779-6790. https://doi.org/10.1039/D4DT00359D