Selective Electrochemical Urea Synthesis from Nitrate and CO2 Using In Situ Ru Anchoring onto a Three-Dimensional Copper Electrode

被引:12
|
作者
Qin, Jiangzhou [1 ]
Liu, Nengsheng [1 ]
Chen, Liuzhou [1 ]
Wu, Kun [1 ]
Zhao, Quanlin [1 ]
Liu, Baojun [2 ]
Ye, Zhengfang [1 ]
机构
[1] Peking Univ, Dept Environm Engn, Key Lab Water & Sediment Sci, Minist Educ, Beijing 100871, Peoples R China
[2] Guizhou Univ, Coll Resource & Environm Engn, Guiyang 550025, Peoples R China
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2022年
基金
中国国家自然科学基金;
关键词
Electrocatalysis; Nitrate recycling; Carbon capture; C-N coupling; Urea synthesis; CARBON-DIOXIDE; REDUCTION; NITROGEN;
D O I
10.1021/acssuschemeng.2c05110
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Urea (CO(NH2)2) is the most common nitrogen fertilizer that is promoting food production worldwide due to its high nitrogen content. However, the conventional urea synthesis involving hydrogenolysis of nitrogen and C-N bond coupling requires harsh conditions and a massive carbon footprint. Herein, we report a promising technology for the green synthesis of urea using nitrate (NO3-) and carbon dioxide (CO2) under ambient conditions over Ru/Pt/Pd-modified three-dimensional copper foam (Ru/Pt/Pd-Cu CF) electrode. The Ru-Cu CF catalyst delivers a high urea yield of 151.6 mu g h-1 cm-2 at a low onset potential of -0.3 V vs Ag/AgCl (0.13 V vs RHE) as well as an FE of 25.4%, surpassing that of Pt/Pd-Cu CF. Moreover, it is confirmed by operando electrocatalytic Raman spectroscopy and theoretical calculations that the *COOH intermediate is the rate-determining step of C-N bond coupling. Benefiting from the partial 3d states of surface Ru sites, the Ru-Cu CF electrode possesses the lowest formation energy of the *COOH intermediate to accelerate the urea synthesis. This work provides an extraordinarily sustainable strategy for green urea synthesis.
引用
收藏
页码:15869 / 15875
页数:7
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