Urea synthesis via electrocatalytic oxidative coupling of CO with NH3 on Pt

被引:14
作者
Xiong, Haocheng [1 ,2 ]
Yu, Peiping [3 ]
Chen, Kedang [2 ]
Lu, Shike [1 ]
Hu, Qikun [1 ]
Cheng, Tao [3 ,4 ]
Xu, Bingjun [2 ]
Lu, Qi [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, State Key Lab Chem Engn, Beijing, Peoples R China
[2] Peking Univ, Coll Chem & Mol Engn, Beijing, Peoples R China
[3] Soochow Univ, Inst Funct Nano & Soft Mat, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Joint Int Res Lab Carbon Based Funct Mat & Devices, Suzhou, Peoples R China
[4] Soochow Univ, Jiangsu Key Lab Adv Negat Carbon Technol, Suzhou, Peoples R China
来源
NATURE CATALYSIS | 2024年 / 7卷 / 07期
基金
中国国家自然科学基金;
关键词
CARBON-MONOXIDE; ELECTROCHEMICAL OXIDATION; ELECTROREDUCTION; PLATINUM; AMMONIA; PT(100); CYANATE; THERMOCHEMISTRY; POLYCRYSTALLINE; ABSORPTION;
D O I
10.1038/s41929-024-01173-w
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
Electrochemical conversion of CO to chemicals containing C-N bonds offers an appealing route to store renewable electricity and mitigate CO2 emission, as CO2 can be efficiently transformed to CO. Previous electrocatalysis research has primarily focused on cathodic reactions, which are impeded by the competing hydrogen evolution reaction and limited electron efficiency. Here we present a urea synthesis approach via electrocatalytic oxidative coupling between CO and NH3 on commercial Pt catalysts. We demonstrate an optimal selectivity of approximately 70% for urea and remain above 50% throughout a wide potential window with an electrocatalytic C-N bond formation rate of up to 100 mmol h(-1) g(catalyst)(-1). In mechanistic investigations, we propose that the oxidative coupling of CO and NH3 on Pt leads to cyanate formation, followed by the W & ouml;hler reaction to form urea. This approach offers a practical route for urea production with high electron efficiency by enabling Pt-catalysed reactions between CO and NH3.
引用
收藏
页码:785 / 795
页数:11
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