Electrochemical N2O reduction reaction catalyzed by a multinuclear copper complex of 1,2,4-triazole
Abstract A trinuclear copper complex of 1,2,4-triazole supported on a carbon black efficiently catalyzes the electrochemical N₂O reduction reaction (e-N2ORR) in alkaline media, achieving 100% Faradaic efficiency at −0.2 V vs. RHE and a turnover frequency up to 267 h⁻¹ at −0.6 V vs. RHE. In situ X-ray absorption spectroscopy reveals that a Cu(0) species produced from the Cu(II) complex under electrochemical conditions is responsible for the high e-N2ORR activity and selectivity, offering a cost-effective strategy for efficient greenhouse gas mitigation.
Authors
- Ichizo Yagi (ORCID: https://orcid.org/0000-0002-4005-9440)
- Masaru Kato (ORCID: https://orcid.org/0000-0002-2845-3525)
- Zhongyi Ma (ORCID: https://orcid.org/0000-0002-7619-4708)
- Takeshi Watanabe (ORCID: https://orcid.org/0000-0001-7850-4178)
Institutions
- Hokkaido University (JP)
- Japan Synchrotron Radiation Research Institute (JP)
Publication Details
- Journal
- Chemistry Letters
- Published
- 2025-07-30
- DOI
- https://doi.org/10.1093/chemle/upaf149
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Hokkaido University