ABSTRACT The electrocatalytic nitrogen reduction reaction (NRR) is a green, low‐energy alternative to the Haber‐Bosch process. This study constructed dual unsaturated vacancies on a stable B 4 N 4 monolayer and designed a B 3 N 4 substrate. The calculation shows that the B 3 N 4 structure has a great stability. The dual atom catalysts (DACs) were constructed through bimetallic doping, denoted as TM 1 TM 2 @B 3 N 4 , for the NRR using a theoretical high‐throughput screening integrated with density functional theory (DFT) calculations. The electrocatalytic NRR performance of the 91 designed DACs was systematically investigated. 4 heteronuclear systems CrZr@B 3 N 4 , CrHf@B 3 N 4 , MnNb@B 3 N 4 , and FeMo@B 3 N 4 were screened out, which are promising NRR electrocatalysts with excellent NRR activities and selectivities using a 3+1 screening strategy. Notably, the designed CrZr@B 3 N 4 demonstrates an outstanding performance with a low limiting potential of −0.16 V along the mixed pathway. Furthermore, a Cascading Associative‐Dissociative (Cascading A–D) reaction mechanism is proposed in which N─N bond scission takes place immediately after the second proton‐coupled electron transfer step ( * N 2 H + H + + e − → * NH * NH). This reaction mechanism was only observed in eight designed electrocatalysts with relatively low activities. This work provides a rational framework for designing high‐performance NRR catalysts and efficient ammonia synthesis.
Cui et al. (Tue,) studied this question.
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