Abstract:

In the industrial landscape, the well-established Haber-Bosch method is employed for the catalytic synthesis of ammonia (NH₃) from hydrogen and nitrogen gases, necessitating elevated temperatures (400-600 ℃) and high pressures (150-300 atm, 1 atm= 0.101325 MPa). In response to the imperative to reduce energy consumption and environment impact imposed by this synthetic process, significant research efforts have converged on realizing NH₃ synthesis under ambient conditions. This study delves into the realm of N₂ electrocatalytic reduction to NH₃, using density functional theory (DFT) calculations to explore the feasibility of employing graphene co-doped with a combination of transition metal elements (e.g., Fe, Nb, Mo, W, and Ru) and non-metal elements (e.g., B, P, and S) as catalyst for ammonia synthesis. The findings underscore that Mo and S co-doped graphene (Mo/S graphene) demonstrates an exceptionally low electrode potential of 0.47 V for NH₃ synthesis, with the key rate-controlling step centered around the formation of the intermediate *NNH. Especially, the ammonia synthesis potential is found to be lower than the hydrogen evolution potential (0.51 V), conclusively affirming the selectivity of nitrogen reduction to ammonia. Furthermore, through ab initio molecular dynamics calculations, the study attests to the remarkable thermodynamic stability of the Mo/S co-doped graphene system under room temperature conditions. Notably, electronic structure analysis validates that the ability of electron communication of the transition metal plays a pivotal role in dictating the efficiency of N₂ electrocatalytic reduction. It can be tactically optimized through controlled modulation of the influence of the non-metal element on the coordination environment of the transition metal, thus substantially enhancing catalytic performance.

Key words: nitrogen reduction reaction, density functional theory, graphene, thermodynamic, electrocatalysis