A replacement strategy for regulating local environment of single-atom Co-SxN4−x catalysts to facilitate CO2 electroreduction
Jiajing Pei,
Huishan Shang,
Junjie Mao,
Zhe Chen,
Rui Sui,
Xuejiang Zhang,
Danni Zhou,
Yu Wang,
Fang Zhang,
Wei Zhu,
Tao Wang (),
Wenxing Chen () and
Zhongbin Zhuang ()
Additional contact information
Jiajing Pei: Beijing University of Chemical Technology
Huishan Shang: Beijing Institute of Technology
Junjie Mao: Anhui Normal University
Zhe Chen: Westlake University
Rui Sui: Beijing University of Chemical Technology
Xuejiang Zhang: Beijing University of Chemical Technology
Danni Zhou: Beijing Institute of Technology
Yu Wang: Chinese Academy of Science
Fang Zhang: Beijing Institute of Technology
Wei Zhu: Beijing University of Chemical Technology
Tao Wang: Westlake University
Wenxing Chen: Beijing Institute of Technology
Zhongbin Zhuang: Beijing University of Chemical Technology
Nature Communications, 2024, vol. 15, issue 1, 1-11
Abstract:
Abstract The performances of single-atom catalysts are governed by their local coordination environments. Here, a thermal replacement strategy is developed for the synthesis of single-atom catalysts with precisely controlled and adjustable local coordination environments. A series of Co-SxN4−x (x = 0, 1, 2, 3) single-atom catalysts are successfully synthesized by thermally replacing coordinated N with S at elevated temperature, and a volcano relationship between coordinations and catalytic performances toward electrochemical CO2 reduction is observed. The Co-S1N3 catalyst has the balanced COOH*and CO* bindings, and thus locates at the apex of the volcano with the highest performance toward electrochemical CO2 reduction to CO, with the maximum CO Faradaic efficiency of 98 ± 1.8% and high turnover frequency of 4564 h−1 at an overpotential of 410 mV tested in H-cell with CO2-saturated 0.5 M KHCO3, surpassing most of the reported single-atom catalysts. This work provides a rational approach to control the local coordination environment of the single-atom catalysts, which is important for further fine-tuning the catalytic performance.
Date: 2024
References: View references in EconPapers View complete reference list from CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-023-44652-7 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-023-44652-7
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-023-44652-7
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().