Boosting Up Electrosynthesis of Urea with Nitrate and Carbon Dioxide via Synergistic Effect of Metallic Iron Cluster and Single‐Atom

Author:

Li Zhiwen123,Xu Mengqiu4,Wang Jiaqian5,Zhang Yifei12,Liu Wen5,Gu Xinrui23,Han Zhong‐Kang5,Ye Wei4,Li Gao123ORCID

Affiliation:

1. Institute of Catalysis for Energy and Environment College of Chemistry and Chemical Engineering Shenyang Normal University Shenyang 110034 P. R. China

2. State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 P. R. China

3. University of Chinese Academy of Sciences Beijing 100049 P. R. China

4. College of Material Chemistry and Chemical Engineering Key Laboratory of Organosilicon Chemistry and Material Technology Ministry of Education Hangzhou Normal University Hangzhou 311121 P. R. China

5. School of Materials Science and Engineering Zhejiang University Hangzhou 310000 P. R. China

Abstract

AbstractElectrocatalytic conversion of nitrates and carbon dioxide to urea under ambient conditions shows promise as a potential substitute for traditional urea synthesis processes characterized by high consumption and pollution. In this study, a straightforward one‐pot method is employed to prepare a highly efficient FeNC‐Fe1N4 electrocatalyst, consisting of atomically dispersed Fe1N4 sites and metallic Fe clusters (FeNC) with particle size of 4–7 nm. The FeNC‐Fe1N4 catalyst exhibits remarkable electrocatalytic activity for urea synthesis from nitrate anion (NO3) and carbon dioxide (CO2), achieving a urea production rate of 38.2 mmol gcat−1 h−1 at −0.9 V (vs RHE) and a Faradaic efficiency of 66.5% at −0.6 V (vs RHE). Both experimental and theoretical results conclusively demonstrate that metallic Fe clusters and Fe1N4 species provide active sites for the adsorption and activation of NO3 and CO2, respectively, and the synergistic effect between Fe1N4 and metallic Fe clusters significantly enhances the electrochemical efficiency of urea synthesis. In all, this work contributes to the rational design and comprehensive synthesis of a dual‐active site iron‐based electrocatalyst, facilitating efficient and sustainable urea synthesis.

Funder

Innovative Research Group Project of the National Natural Science Foundation of China

Publisher

Wiley

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