Electrocatalytic Urea Production with Nitrate and CO<sub>2</sub> on a Ru‐Dispersed Co Catalyst

Abstract Urea electrosynthesis from co‐electrolysis of NO 3 − and CO 2 (UENC) provides an alternative route for realizing efficient and sustainable urea production. In this work, single‐atom Ru dispersed on Co (Ru 1 Co) is demonstrated as an effective and robust catalyst for the UENC. In situ spectroscopic measurements and theoretical simulations unravel the cooperative effect of Ru 1 and Co sites to promote the UENC process via a tandem catalysis mechanism, where the Ru 1 site activates the adsorption and hydrogenation of NO 3 − to form * NH 2 , while the Co site activates the adsorption and hydrogenation/deoxygenation of CO 2 to form * CO. The generated * CO is then transferred from the Co site to the nearby Ru 1 site which promotes the C─N coupling of * NH 2 and * CO toward the urea formation. Strikingly, Ru 1 Co assembled in a flow cell shows the highest urea‐Faradaic efficiency of 50.1% with the corresponding urea yield rate of 22.34 mmol h −1 g −1 at −0.5 V (RHE), superior to most reported UENC catalysts for urea production.

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Publication Details

Journal
Advanced Functional Materials
Published
2024-08-12
DOI
https://doi.org/10.1002/adfm.202406438
Citations
32
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
3.42

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article

Electrocatalytic Urea Production with Nitrate and CO2 on a Ru‐Dispersed Co Catalyst

Ke Chu, Zhuoyan Zhang, Xing Yang, Hu Zhang et al.
32 citations
Advanced Functional Materials
Ammonia Synthesis and Nitrogen Reduction
3.42
article

Electrocatalytic Urea Production with Nitrate and CO2 on a Ru‐Dispersed Co Catalyst

Ke Chu, Zhuoyan Zhang, Xing Yang, Hu Zhang, Yuying Wan, Xiaomei Wang
article en
32 citations

Abstract

Abstract Urea electrosynthesis from co‐electrolysis of NO 3 − and CO 2 (UENC) provides an alternative route for realizing efficient and sustainable urea production. In this work, single‐atom Ru dispersed on Co (Ru 1 Co) is demonstrated as an effective and robust catalyst for the UENC. In situ spectroscopic measurements and theoretical simulations unravel the cooperative effect of Ru 1 and Co sites to promote the UENC process via a tandem catalysis mechanism, where the Ru 1 site activates the adsorption and hydrogenation of NO 3 − to form * NH 2 , while the Co site activates the adsorption and hydrogenation/deoxygenation of CO 2 to form * CO. The generated * CO is then transferred from the Co site to the nearby Ru 1 site which promotes the C─N coupling of * NH 2 and * CO toward the urea formation. Strikingly, Ru 1 Co assembled in a flow cell shows the highest urea‐Faradaic efficiency of 50.1% with the corresponding urea yield rate of 22.34 mmol h −1 g −1 at −0.5 V (RHE), superior to most reported UENC catalysts for urea production.

Advanced Functional MaterialsVol. 34(41)
Lanzhou Jiaotong University (CN), University of Science and Technology Beijing (CN)
National Natural Science Foundation of China, Gansu Education Department
Responsible consumption and production
Openalex Percentile: Top 6%
Ammonia Synthesis and Nitrogen Reduction
3.42
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