2021/02/26 by Menglei Yuan, Junwu Chen, Yiling Bai +7 · 6 citations
Chemical Engineering · Energy · #Advanced Photocatalysis Techniques #Ammonia Synthesis and Nitrogen Reduction #CO2 Reduction Techniques and Catalysts
paper · doi:10.1002/anie.202101275
openalex publication_date 2021/02/26 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/28
Abstract Electrocatalytic C−N bond coupling to convert CO 2 and N 2 molecules into urea under ambient conditions is a promising alternative to harsh industrial processes. However, the adsorption and activation of inert gas molecules and then the driving of the C–N coupling reaction is energetically challenging. Herein, novel Mott–Schottky Bi‐BiVO 4 heterostructures are described that realize a remarkable urea yield rate of 5.91 mmol h −1 g −1 and a Faradaic efficiency of 12.55 % at −0.4 V vs. RHE. Comprehensive analysis confirms the emerging space–charge region in the heterostructure interface not only facilitates the targeted adsorption and activation of CO 2 and N 2 molecules on the generated local nucleophilic and electrophilic regions, but also effectively suppresses CO poisoning and the formation of endothermic *NNH intermediates. This guarantees the desired exothermic coupling of *N=N* intermediates and generated CO to form the urea precursor, *NCON*.