Electrochemical Oxidation of Methane to Methylamine
The electrochemical methane (CH<sub>4</sub>) oxidation reaction under ambient conditions is a promising approach for natural gas utilization. However, the highly stable nature of CH<sub>4</sub> restrains efficient cleavage of the C-H bond without overoxidation. To this end, we proposed a coupled oxidative strategy for converting CH<sub>4</sub> to value-added products via NH<sub>2</sub> intermediates. The ammonia-oxidation-driven anodic reaction facilitates the formation of NH<sub>2</sub> species and activates CH<sub>4</sub> through nucleophilic attack to achieve C-N bond formation. Further the generated methylamine could be protected from overoxidation in the ammonia-based anolyte. Under such conditions, a methylamine productivity of 3.8 mmol g<sup>-1</sup><sub>cat</sub> h<sup>-1</sup> at 1.55 V vs a reversible hydrogen electrode is reported. This work provides new insights into electrocatalytic C-N coupling based on the ammonia oxidation reaction, which could extend to other alkane or alkene conversions.
Authors
- Qiang Song (ORCID: https://orcid.org/0000-0001-6231-8303)
- Patrick J. Cullen (ORCID: https://orcid.org/0000-0001-7654-6171)
- Jungmi Hong (ORCID: https://orcid.org/0000-0002-6998-9502)
- Wanping Xu
- Tianqi Zhang (ORCID: https://orcid.org/0000-0002-6256-0877)
- Xin Zeng (ORCID: https://orcid.org/0000-0001-9204-1616)
Institutions
- The University of Sydney (AU)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-04-25
- DOI
- https://doi.org/10.1021/jacs.5c04802
- Citations
- 4
- Primary Topic
- Catalysis and Oxidation Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.56
Funders
- Australian Research Council