Electrochemical reduction of nitrate to ammonia is not only an effective strategy for dealing with nitrate pollution but also presents a promising alternative in the field of ammonia synthesis at low temperatures. Nevertheless, current research on nitrate reduction reactions (NO3RR) has predominantly centered on metal catalyst systems, and owing to an incomplete understanding of the catalytic mechanism, the development of this field still faces significant challenges. This research employs density functional theory (DFT) computations to systematically explore the catalytic capability of single-atom nonmetallic catalysts (NM/g-C2N) embedded in nitrogen-doped porous graphene (g-C2N) for the reduction of nitrate to ammonia (NO3RR-to-NH3). Findings reveal that Si/g-C2N and As/g-C2N systems showcase remarkable electrocatalytic activity for NO3RR, with limiting potentials for ammonia synthesis as low as -0.23 V and -0.31 V, respectively. Crucially, higher energy barriers effectively inhibit the formation of byproducts (NO2-, NO, N2), thereby boosting ammonia synthesis selectivity. Additionally, the hydrogen evolution reaction (HER) is thermodynamically suppressed due to weak hydrogen adsorption on the catalyst surface. This study not only discovers a new type of NO3RR catalyst but also provides new ideas and methods for designing novel NO3RR catalysts.
Zhang et al. (Fri,) studied this question.