FeNi3 nanoparticles for electrocatalytic synthesis of urea from carbon dioxide and nitrate

被引:37
|
作者
Hou, Tong [1 ,2 ,3 ]
Ding, Junyang [4 ]
Zhang, Hao [4 ]
Chen, Shanshan [4 ]
Liu, Qian [5 ]
Luo, Jun [6 ]
Liu, Xijun [1 ,2 ,3 ]
机构
[1] Sch Resource, MOE Key Lab New Proc Technol Nonferrous Met & Mat, Environm & Mat, Nanning 530004, Peoples R China
[2] Sch Resource, Guangxi Key Lab Proc Nonferrous Met & Featured Mat, Nanning 530004, Peoples R China
[3] Guangxi Univ, Sch Chem & Chem Engn, Guangxi Key Lab Electrochem Energy Mat, 100 Daxue Rd, Nanning 530004, Peoples R China
[4] Tianjin Univ Technol, Inst New Energy Mat & Low Carbon Technol, Sch Mat Sci & Engn, Tianjin 300384, Peoples R China
[5] Chengdu Univ, Inst Adv Study, Chengdu 610106, Sichuan, Peoples R China
[6] Univ Elect Sci & Technol China, Shenzhen Inst Adv Study, ShenSi Lab, Shenzhen 518110, Peoples R China
基金
中国国家自然科学基金;
关键词
REDUCTION;
D O I
10.1039/d3qm00627a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Due to the environmental pollution and high energy consumption associated with the conventional industrial Bosch-Meiser method, electrocatalytic urea synthesis emerges as a promising and sustainable alternative route. In this work, we constructed and utilized nitrogen-doped porous carbon loaded with bimetallic FeNi3 alloy nanoparticles as an efficient electrocatalyst for synthesizing urea from carbon dioxide (CO2) and nitrate (NO3-). The created FeNi3 alloy within FeNi/NC served as the active site for the C-N coupling reaction, generating a higher urea yield of 496.5 & mu;g h(-1) mg(cat.)(-1) with a correlating faradaic efficiency (FE) of 16.58% at -0.9 V versus the reversible hydrogen electrode (vs. RHE), when in comparison to monometallic Fe/NC and Ni/NC catalysts. Moreover, we also monitored the urea generation process via in situ Raman spectroscopy technology, which enabled the identification of two critical reaction species, namely O-C-O and N-C-N, inferring that C-N coupling acted as the key reaction step.
引用
收藏
页码:4952 / 4960
页数:9
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