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Efficient urea electrosynthesis from carbon dioxide and nitrate via alternating Cu-W bimetallic C-N coupling sites.


ABSTRACT: Electrocatalytic urea synthesis is an emerging alternative technology to the traditional energy-intensive industrial urea synthesis protocol. Novel strategies are urgently needed to promote the electrocatalytic C-N coupling process and inhibit the side reactions. Here, we report a CuWO4 catalyst with native bimetallic sites that achieves a high urea production rate (98.5 ± 3.2 μg h-1 mg-1cat) for the co-reduction of CO2 and NO3- with a high Faradaic efficiency (70.1 ± 2.4%) at -0.2 V versus the reversible hydrogen electrode. Mechanistic studies demonstrated that the combination of stable intermediates of *NO2 and *CO increases the probability of C-N coupling and reduces the potential barrier, resulting in high Faradaic efficiency and low overpotential. This study provides a new perspective on achieving efficient urea electrosynthesis by stabilizing the key reaction intermediates, which may guide the design of other electrochemical systems for high-value C-N bond-containing chemicals.

SUBMITTER: Zhao Y 

PROVIDER: S-EPMC10372083 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature

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Efficient urea electrosynthesis from carbon dioxide and nitrate via alternating Cu-W bimetallic C-N coupling sites.

Zhao Yilong Y   Ding Yunxuan Y   Li Wenlong W   Liu Chang C   Li Yingzheng Y   Zhao Ziqi Z   Shan Yu Y   Li Fei F   Sun Licheng L   Li Fusheng F  

Nature communications 20230726 1


Electrocatalytic urea synthesis is an emerging alternative technology to the traditional energy-intensive industrial urea synthesis protocol. Novel strategies are urgently needed to promote the electrocatalytic C-N coupling process and inhibit the side reactions. Here, we report a CuWO<sub>4</sub> catalyst with native bimetallic sites that achieves a high urea production rate (98.5 ± 3.2 μg h<sup>-1</sup> mg<sup>-1</sup><sub>cat</sub>) for the co-reduction of CO<sub>2</sub> and NO<sub>3</sub><su  ...[more]

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