Urea Synthesis via Coelectrolysis of CO2 and Nitrate over Heterostructured Cu-Bi Catalysts

被引:10
|
作者
Song, Xinning [1 ,2 ]
Ma, Xiaodong [1 ,2 ]
Chen, Tianhui [3 ]
Xu, Liang [1 ,4 ]
Feng, Jiaqi [1 ]
Wu, Limin [1 ,2 ]
Jia, Shunhan [1 ,2 ]
Zhang, Libing [1 ,2 ]
Tan, Xingxing [1 ,2 ]
Wang, Ruhan [1 ,2 ]
Chen, Chunjun [1 ,5 ]
Ma, Jun [1 ]
Zhu, Qinggong [1 ,2 ]
Kang, Xinchen [1 ,2 ]
Sun, Xiaofu [1 ,2 ]
Han, Buxing [1 ,2 ,5 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Key Lab Colloid & Interface & Thermodynam, Ctr Carbon Neutral Chem,Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[3] Nankai Univ, Coll Chem, Tianjin 300071, Peoples R China
[4] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[5] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, State Key Lab Petr Mol & Proc Engn, Shanghai 200062, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Bismuth alloys - Copper alloys - Greenhouse gas emissions - Industrial emissions - Kyoto Protocol;
D O I
10.1021/jacs.4c08564
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic coupling of CO(2 )and NO3 - to urea is a promising way to mitigate greenhouse gas emissions, reduce waste from industrial processes, and store renewable energy. However, the poor selectivity and activity limit its application due to the multistep process involving diverse reactants and reactions. Herein, we report the first work to design heterostructured Cu-Bi bimetallic catalysts for urea electrosynthesis. A high urea Faradaic efficiency (FE) of 23.5% with a production rate of 2180.3 mu g h(-1) mg(cat)(-1) was achieved in H-cells, which surpassed most reported electrocatalysts in the literature. Moreover, the catalyst had a remarkable recycling stability. Experiments and density functional theory calculations demonstrated that introduction of moderate Bi induced the formation of the Bi-Cu/O-Bi/Cu2O heterostructure with abundant phase boundaries, which are beneficial for NO3 -, CO2, and H2O activation and enhance C-N coupling and promote *HONCON intermediate formation. Moreover, favorable *HNCONH2 protonation and urea desorption processes were also validated, further explaining the reason for high activity and selectivity toward urea.
引用
收藏
页码:25813 / 25823
页数:11
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