Zhiwen Li, Mengqiu Xu, Jiaqian Wang, Yifei Zhang, Wen Liu, Xinrui Gu, Zhong-Kang Han, Wei Ye, Gao Li
{"title":"Boosting Up Electrosynthesis of Urea with Nitrate and Carbon Dioxide via Synergistic Effect of Metallic Iron Cluster and Single-Atom","authors":"Zhiwen Li, Mengqiu Xu, Jiaqian Wang, Yifei Zhang, Wen Liu, Xinrui Gu, Zhong-Kang Han, Wei Ye, Gao Li","doi":"10.1002/smll.202400036","DOIUrl":null,"url":null,"abstract":"<p>Electrocatalytic 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-Fe<sub>1</sub>N<sub>4</sub> electrocatalyst, consisting of atomically dispersed Fe<sub>1</sub>N<sub>4</sub> sites and metallic Fe clusters (FeNC) with particle size of 4–7 nm. The FeNC-Fe<sub>1</sub>N<sub>4</sub> catalyst exhibits remarkable electrocatalytic activity for urea synthesis from nitrate anion (NO<sub>3</sub><sup>−</sup>) and carbon dioxide (CO<sub>2</sub>), achieving a urea production rate of 38.2 mmol g<sub>cat</sub><sup>−1</sup> h<sup>−1</sup> 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 Fe<sub>1</sub>N<sub>4</sub> species provide active sites for the adsorption and activation of NO<sub>3</sub><sup>−</sup> and CO<sub>2</sub>, respectively, and the synergistic effect between Fe<sub>1</sub>N<sub>4</sub> 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.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"20 38","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202400036","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Electrocatalytic 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.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.