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Electrochemical coreduction of carbon dioxide and nitrate offers a sustainable pathway to synthesize value-added urea from greenhouse gas and nitrogen-containing waste; however, challenges remain in designing efficient catalysts. Based on the concept of “integrative catalytic pairs (ICPs)”, a catalyst for urea synthesis is designed by introducing heteroatoms (B and C) into M–N–C, where a single transition metal is dispersed on N-doped carbon material. Using a two-step theoretical screening strategy, Ni–N 3 B is identified as a promising catalyst for urea synthesis, with a low limiting potential (−0.43 V) and a small kinetic barrier for C–N coupling (0.74 eV) due to the electronic regulation effects and the synergy of Ni and B function for enhancing NO 3 – activation and facilitating C–N coupling between gaseous CO 2 and *NH intermediate. Under the guidance of these theoretical results, our further experimental validation demonstrates that the synthesized Ni–N 3 B catalyst achieves a Faradaic efficiency of 51.92% and a urea yield rate of 32.30 mmol h –1 g –1 at −0.6 V vs RHE. Our work not only identifies an efficient urea synthesis catalyst without relying on trial-and-error methods but also inspires further exploration of ICPs-based catalysts in electrocatalysis.
Su et al. (Thu,) studied this question.