Electrochemical Synthesis of Urea: Co-reduction of Nitric Oxide and Carbon Monoxide

被引:0
作者
Wan, Hao [1 ]
Wang, Xingli [3 ]
Tan, Lei [3 ]
Filippi, Michael [3 ]
Strasser, Peter [3 ]
Rossmeisl, Jan [1 ]
Bagger, Alexander [1 ,2 ]
机构
[1] Univ Copenhagen, Ctr High Entropy Alloy Catalysis CHEAC, Dept Chem, DK-2100 Copenhagen, Denmark
[2] Imperial Coll London, Royal Sch Mines 2 03b, Dept Chem Engn, London SW7 2AZ, England
[3] Tech Univ Berlin, Dept Chem, Chem Engn Div, D-10623 Berlin, Germany
来源
ACS CATALYSIS | 2023年
基金
新加坡国家研究基金会;
关键词
DFT Simulations; Electrocatalysis; C-N coupling; NOx Removal; Urea Synthesis;
D O I
暂无
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrocatalytic conversion is a promising technology for storing renewable electricity in the chemical form. Substantial efforts have been made on the multicarbon feedstock production, while little is known about producing nitrogen containing chemicals like urea via C-N coupling. Here, we elucidate the possible urea production on metals through coreduction of nitric oxide (NO) and carbon oxide (CO). Based on adsorption energies calculated by density functional theory (DFT), we find that Cu is able to bind both *NO and *CO while not binding *H. During NO + CO coreduction, we identify two kinetically and thermodynamically possible C-N couplings via *CO + *N and *CONH + *N, and further hydrogenation leads to urea formation. A 2-D activity heatmap has been constructed for describing nitrogen conversion to urea. This work provides a clear example of using computational simulations to predict selective and active materials for urea production.
引用
收藏
页码:1926 / 1933
页数:8
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