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Unveiling Electrochemical Urea Synthesis by Co-Activation of CO2 and N-2 with Mott-Schottky Heterostructure Catalysts | |
Yuan, Menglei1,2; Chen, Junwu1,2; Bai, Yiling3,4; Liu, Zhanjun2,3; Zhang, Jingxian1,2; Zhao, Tongkun1,2; Wang, Qin5; Li, Shuwei1,2; He, Hongyan1,2; Zhang, Guangjin1,2,6 | |
2021-04-08 | |
Source Publication | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
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ISSN | 1433-7851 |
Pages | 10 |
Abstract | Electrocatalytic C-N bond coupling to convert CO2 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-BiVO4 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 CO2 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*. |
Keyword | C– N coupling electrocatalysis Mott– Schottky heterostructures urea |
DOI | 10.1002/anie.202101275 |
Language | 英语 |
Funding Project | National Key R&D Program of China[2020YFA0710200] ; Chemistry and Chemical Engineering Guangdong Laboratory[1922006] ; Key Program for International S&T Cooperation Projects - Ministry of Science and Technology of China[2018YFE0124600] |
WOS Research Area | Chemistry |
WOS Subject | Chemistry, Multidisciplinary |
Funding Organization | National Key R&D Program of China ; Chemistry and Chemical Engineering Guangdong Laboratory ; Key Program for International S&T Cooperation Projects - Ministry of Science and Technology of China |
WOS ID | WOS:000637979200001 |
Publisher | WILEY-V C H VERLAG GMBH |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://ir.ipe.ac.cn/handle/122111/48145 |
Collection | 中国科学院过程工程研究所 |
Corresponding Author | Zhang, Guangjin |
Affiliation | 1.Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, CAS Key Lab Green Proc Engn, Beijing 100190, Peoples R China 2.Univ Chinese Acad Sci, Ctr Mat Sci & Optoelet Engn, Beijing 100049, Peoples R China 3.Chinese Acad Sci, Inst Coal Chem, CAS Key Lab Carbon Mat, Taiyuan 030001, Peoples R China 4.Synfuels China Technol Co Ltd, SynCat Beijing, Beijing 101407, Peoples R China 5.Hebei Enco Petrochem Engn Co Ltd, Engn Design Dept, Henan Branch, Zhengzhou 450000, Henan, Peoples R China 6.Chem & Chem Engn Guangdong Lab, Shantou 515031, Peoples R China |
Recommended Citation GB/T 7714 | Yuan, Menglei,Chen, Junwu,Bai, Yiling,et al. Unveiling Electrochemical Urea Synthesis by Co-Activation of CO2 and N-2 with Mott-Schottky Heterostructure Catalysts[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,2021:10. |
APA | Yuan, Menglei.,Chen, Junwu.,Bai, Yiling.,Liu, Zhanjun.,Zhang, Jingxian.,...&Zhang, Guangjin.(2021).Unveiling Electrochemical Urea Synthesis by Co-Activation of CO2 and N-2 with Mott-Schottky Heterostructure Catalysts.ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,10. |
MLA | Yuan, Menglei,et al."Unveiling Electrochemical Urea Synthesis by Co-Activation of CO2 and N-2 with Mott-Schottky Heterostructure Catalysts".ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2021):10. |
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