Ambient Electrosynthesis of Urea with Nitrate and Carbon Dioxide over Iron-Based Dual-Sites

被引:113
|
作者
Geng, Jing [1 ,2 ]
Ji, Sihan [1 ,2 ]
Jin, Meng [1 ,2 ]
Zhang, Chao [2 ]
Xu, Min [1 ,2 ]
Wang, Guozhong [1 ,2 ]
Liang, Changhao [1 ,2 ]
Zhang, Haimin [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Solid State Phys, CAS Ctr Excellence Nanosci, Ctr Environm & Energy Nanomat,Key Lab Mat Phys,Anh, Hefei 230031, Peoples R China
[2] Univ Sci & Technol China, Hefei 230026, Peoples R China
关键词
Amorphous Fe Nanoparticles; C-N Coupling Reaction; Dual Active Sites; Fe3O4; Nanoparticles; Urea; ELECTROCATALYTIC N-2 REDUCTION; ATMOSPHERIC-PRESSURE; AMMONIA-SYNTHESIS; EFFICIENT; HYDROGEN; NANOPARTICLES; TEMPERATURE; CONVERSION; COMPOSITE; NITROGEN;
D O I
10.1002/anie.202210958
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of efficient electrocatalysts to generate key *NH2 and *CO intermediates is crucial for ambient urea electrosynthesis with nitrate (NO3-) and carbon dioxide (CO2). Here we report a liquid-phase laser irradiation method to fabricate symbiotic graphitic carbon encapsulated amorphous iron and iron oxide nanoparticles on carbon nanotubes (Fe(a)@C-Fe3O4/CNTs). Fe(a)@C-Fe3O4/CNTs exhibits superior electrocatalytic activity toward urea synthesis using NO3- and CO2, affording a urea yield of 1341.3 +/- 112.6 mu g h(-1) mg(cat)(-1) and a faradic efficiency of 16.5 +/- 6.1 % at ambient conditions. Both experimental and theoretical results indicate that the formed Fe(a)@C and Fe3O4 on CNTs provide dual active sites for the adsorption and activation of NO3- and CO2, thus generating key *NH2 and *CO intermediates with lower energy barriers for urea formation. This work would be helpful for design and development of high-efficiency dual-site electrocatalysts for ambient urea synthesis.
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页数:7
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