Amorphous Bismuth-Tin Oxide Nanosheets with Optimized C-N Coupling for Efficient Urea Synthesis

被引:54
作者
Chen, Xiangyu [1 ]
Lv, Shuning [2 ]
Gu, Hongfei [1 ]
Cui, Hanke [1 ]
Liu, Gui [1 ]
Liu, Yifei [1 ]
Li, Zhaoyu [1 ]
Xu, Ziyan [1 ]
Kang, Jianxin [1 ]
Teobaldi, Gilberto [3 ]
Liu, Li-Min [2 ]
Guo, Lin [1 ]
机构
[1] Beihang Univ, Sch Chem, Beijing Adv Innovat Ctr Biomed Engn, Key Lab Bioinspired Smart Interfacial Sci & Techno, Beijing 100191, Peoples R China
[2] Beihang Univ, Sch Phys, Beijing 100191, Peoples R China
[3] Rutherford Appleton Lab, Sci Comp Dept, STFC UKRI, Didcot OX11 0QX, England
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CARBON-DIOXIDE; NITRITE; REDUCTION;
D O I
10.1021/jacs.4c03156
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Closing the carbon and nitrogen cycles by electrochemical methods using renewable energy to convert abundant or harmful feedstocks into high-value C- or N-containing chemicals has the potential to transform the global energy landscape. However, efficient conversion avenues have to date been mostly realized for the independent reduction of CO2 or NO3-. The synthesis of more complex C-N compounds still suffers from low conversion efficiency due to the inability to find effective catalysts. To this end, here we present amorphous bismuth-tin oxide nanosheets, which effectively reduce the energy barrier of the catalytic reaction, facilitating efficient and highly selective urea production. With enhanced CO2 adsorption and activation on the catalyst, a C-N coupling pathway based on *CO2 rather than traditional *CO is realized. The optimized orbital symmetry of the C- (*CO2) and N-containing (*NO2) intermediates promotes a significant increase in the Faraday efficiency of urea production to an outstanding value of 78.36% at -0.4 V vs RHE. In parallel, the nitrogen and carbon selectivity for urea formation is also enhanced to 90.41% and 95.39%, respectively. The present results and insights provide a valuable reference for the further development of new catalysts for efficient synthesis of high-value C-N compounds from CO2.
引用
收藏
页码:13527 / 13535
页数:9
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