TY - JOUR
T1 - Urea Synthesis via Coelectrolysis of CO2 and Nitrate over Heterostructured Cu-Bi Catalysts
AU - Song, Xinning
AU - Ma, Xiaodong
AU - Chen, Tianhui
AU - Xu, Liang
AU - Feng, Jiaqi
AU - Wu, Limin
AU - Jia, Shunhan
AU - Zhang, Libing
AU - Tan, Xingxing
AU - Wang, Ruhan
AU - Chen, Chunjun
AU - Ma, Jun
AU - Zhu, Qinggong
AU - Kang, Xinchen
AU - Sun, Xiaofu
AU - Han, Buxing
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/9/18
Y1 - 2024/9/18
N2 - Electrocatalytic coupling of CO2 and NO3- to urea is a promising way to mitigate greenhouse gas emissions, reduce waste from industrial processes, and store renewable energy. However, the poor selectivity and activity limit its application due to the multistep process involving diverse reactants and reactions. Herein, we report the first work to design heterostructured Cu-Bi bimetallic catalysts for urea electrosynthesis. A high urea Faradaic efficiency (FE) of 23.5% with a production rate of 2180.3 μg h-1 mgcat-1 was achieved in H-cells, which surpassed most reported electrocatalysts in the literature. Moreover, the catalyst had a remarkable recycling stability. Experiments and density functional theory calculations demonstrated that introduction of moderate Bi induced the formation of the Bi-Cu/O-Bi/Cu2O heterostructure with abundant phase boundaries, which are beneficial for NO3-, CO2, and H2O activation and enhance C-N coupling and promote *HONCON intermediate formation. Moreover, favorable *HNCONH2 protonation and urea desorption processes were also validated, further explaining the reason for high activity and selectivity toward urea.
AB - Electrocatalytic coupling of CO2 and NO3- to urea is a promising way to mitigate greenhouse gas emissions, reduce waste from industrial processes, and store renewable energy. However, the poor selectivity and activity limit its application due to the multistep process involving diverse reactants and reactions. Herein, we report the first work to design heterostructured Cu-Bi bimetallic catalysts for urea electrosynthesis. A high urea Faradaic efficiency (FE) of 23.5% with a production rate of 2180.3 μg h-1 mgcat-1 was achieved in H-cells, which surpassed most reported electrocatalysts in the literature. Moreover, the catalyst had a remarkable recycling stability. Experiments and density functional theory calculations demonstrated that introduction of moderate Bi induced the formation of the Bi-Cu/O-Bi/Cu2O heterostructure with abundant phase boundaries, which are beneficial for NO3-, CO2, and H2O activation and enhance C-N coupling and promote *HONCON intermediate formation. Moreover, favorable *HNCONH2 protonation and urea desorption processes were also validated, further explaining the reason for high activity and selectivity toward urea.
UR - https://www.scopus.com/pages/publications/85203172267
U2 - 10.1021/jacs.4c08564
DO - 10.1021/jacs.4c08564
M3 - 文章
C2 - 39236157
AN - SCOPUS:85203172267
SN - 0002-7863
VL - 146
SP - 25813
EP - 25823
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 37
ER -