Single-Atom Rh<sub>1</sub> Alloyed Co for Urea Electrosynthesis from CO<sub>2</sub> and NO<sub>3</sub><sup>–</sup>

Single-atom Rh<sub>1</sub> alloyed Co (Rh<sub>1</sub>Co) is explored as an efficient catalyst for urea electrosynthesis via coelectrolysis of CO<sub>2</sub> and NO<sub>3</sub><sup>-</sup> (UECN). Theoretical calculations and in situ spectroscopic measurements unravel the synergetic effect of Co and Rh<sub>1</sub> in promoting the UECN process, where the Rh<sub>1</sub> site activates NO<sub>3</sub><sup>-</sup> to form *NH<sub>2</sub>, while the Co site activates CO<sub>2</sub> to form *CO. The formed *CO then desorbs from the Co site and transfers to the Rh<sub>1</sub> site, followed by continuous C-N coupling with *NH<sub>2</sub> formed on the Rh<sub>1</sub> site to synthesize urea. Remarkably, Rh<sub>1</sub>Co assembled in a flow cell delivers the exceptional urea yield rate of 24.9 mmol h<sup>-1</sup> g<sup>-1</sup> and Faradaic efficiency of 51.1%, outperforming most previously reported UECN catalysts.

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Publication Details

Journal
Nano Letters
Published
2024-08-20
DOI
https://doi.org/10.1021/acs.nanolett.4c02767
Citations
25
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
Type
article
Field-Weighted Citation Impact
2.67

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article

Single-Atom Rh1 Alloyed Co for Urea Electrosynthesis from CO2 and NO3–

Zhuoyan Zhang, Yicheng Wei, Jinmei Qian, Yuying Wan et al.
25 citations
Nano Letters
Ammonia Synthesis and Nitrogen Reduction
2.67
article

Single-Atom Rh1 Alloyed Co for Urea Electrosynthesis from CO2 and NO3–

Zhuoyan Zhang, Yicheng Wei, Jinmei Qian, Yuying Wan, Ke Chu, Jilong Kang
article en
25 citations

Abstract

Single-atom Rh<sub>1</sub> alloyed Co (Rh<sub>1</sub>Co) is explored as an efficient catalyst for urea electrosynthesis via coelectrolysis of CO<sub>2</sub> and NO<sub>3</sub><sup>-</sup> (UECN). Theoretical calculations and in situ spectroscopic measurements unravel the synergetic effect of Co and Rh<sub>1</sub> in promoting the UECN process, where the Rh<sub>1</sub> site activates NO<sub>3</sub><sup>-</sup> to form *NH<sub>2</sub>, while the Co site activates CO<sub>2</sub> to form *CO. The formed *CO then desorbs from the Co site and transfers to the Rh<sub>1</sub> site, followed by continuous C-N coupling with *NH<sub>2</sub> formed on the Rh<sub>1</sub> site to synthesize urea. Remarkably, Rh<sub>1</sub>Co assembled in a flow cell delivers the exceptional urea yield rate of 24.9 mmol h<sup>-1</sup> g<sup>-1</sup> and Faradaic efficiency of 51.1%, outperforming most previously reported UECN catalysts.

Nano LettersVol. 24(35)
Lanzhou Jiaotong University (CN)
National Natural Science Foundation of China, Lanzhou Jiaotong University
Openalex Percentile: Top 8%
Ammonia Synthesis and Nitrogen Reduction
2.67
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