Boosting the efficiency of urea synthesis via cooperative electroreduction of N2 and CO2 on MoP

被引:57
|
作者
Jiao, Dongxu [1 ,5 ]
Dong, Yilong [5 ]
Cui, Xiaoqiang [5 ]
Cai, Qinghai [1 ,4 ]
Cabrera, Carlos R. [2 ]
Zhao, Jingxiang [1 ]
Chen, Zhongfang [3 ]
机构
[1] Harbin Normal Univ, Coll Chem & Chem Engn, Key Lab Photon & Elect Bandgap Mat, Minist Educ, Harbin 150025, Peoples R China
[2] Univ Texas El Paso, Dept Chem & Biochem, El Paso, TX 79968 USA
[3] Univ Puerto Rico, Dept Chem, Rio Piedras Campus, San Juan, PR 00931 USA
[4] Heilongjiang Prov Collaborat Innovat Ctr Cold Reg, Harbin 150025, Peoples R China
[5] Jilin Univ, Sch Mat Sci & Engn, State Key Lab Automot Simulat & Control, Key Lab Automobile Mat MOE, Changchun 130012, Peoples R China
基金
黑龙江省自然科学基金; 中国国家自然科学基金;
关键词
MOLYBDENUM PHOSPHIDE NANOPARTICLES; HYDROGEN EVOLUTION; AMMONIA-SYNTHESIS; ELECTROCATALYST; CHALLENGES; REDUCTION; CATALYSTS; NITROGEN;
D O I
10.1039/d2ta07531h
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
By combining theoretical and experimental efforts, we designed the MoP-(101) surface and explored its potential as catalyst for urea production. Our computations revealed that N-2 and CO2 reactants can be effectively reduced to urea on the MoP-(101) surface with a low limiting potential (-0.27 V); the competitive side reactions are well suppressed, and the *NHCONH species is a key reaction intermediate for the C-N coupling during urea synthesis. Our experimental measurements confirmed the above theoretical predictions: urea synthesis was achieved with the urea formation rate of 12.4 mu g h(-1) mg(-1) and the faradaic efficiency of 36.5%. This work not only highlights the critical role of the abundant Mo active sites for urea electrosynthesis but also provides a new mechanism for C-N coupling, which may be used to further develop other efficient electrocatalysts.
引用
收藏
页码:232 / 240
页数:9
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