Regulating Efficient and Selective Single-atom Catalysts for Electrocatalytic CO2 Reduction

Anchoring transition metal (TM) atoms on suitable substrates to form single-atom catalysts (SACs) is a novel approach to constructing electrocatalysts. Graphdiyne with sp?sp² hybridized carbon atoms and uniformly distributed pores have been considered as a potential carbon material for supporting metal atoms in a variety of catalytic processes. Herein, density functional theory (DFT) calculations were performed to study the single TM atom anchoring on graphdiyne (TM₁?GDY, TM=Sc, Ti, V, Cr, Mn, Co and Cu) as the catalysts for CO₂ reduction. After anchoring metal atoms on GDY, the catalytic activity of TM₁?GDY (TM=Mn, Co and Cu) for CO₂ reduction reaction (CO₂RR) are significantly improved comparing with the pristine GDY. Among the studied TM₁?GDY, Cu₁?GDY shows excellent electrocatalytic activity for CO₂ reduction for which the product is HCOOH and the limiting potential (U_L) is ?0.16 V. Mn₁?GDY and Co₁?GDY exhibit superior catalytic selectivity for CO₂ reduction to CH₄ with U_L of ?0.62 and ?0.34 V, respectively. The hydrogen evolution reaction (HER) by TM₁?GDY (TM=Mn, Co and Cu) occurs on carbon atoms, while the active sites of CO₂RR are the transition metal atoms . The present work is expected to provide a solid theoretical basis for CO₂ conversion into valuable hydrocarbons.