Water‐Enabled CO <sub>2</sub> Hydrogenation to Ethanol via a Mixed‐Potential‐Driven Mechanism
Ethanol synthesis from CO<sub>2</sub> and H<sub>2</sub> is currently a hot topic of research in heterogeneous catalysis. However, the underlying mechanism has not yet been clearly elucidated. We propose that the synthesis involves several other reactions on the electrode surface, as evident by the formation of a mixed potential. In this study, we prepared solid catalysts, Ru/CoO<sub>x</sub> and CuPd/C, as the nano-anode and nano-cathode components and carried out CO<sub>2</sub> hydrogenation in the presence of small amounts of water to facilitate ion conduction. Ethanol was produced along with CO, CH<sub>4</sub>, and methanol at reaction temperatures below 473 K in the presence of both the catalysts. The activation energy for ethanol formation with Ru/CoO<sub>x</sub> was found to be 25 ± 5 kJ mol<sup>-1</sup>, which was much lower than those for the formations of CO (44 ± 4 kJ mol<sup>-1</sup>), CH<sub>4</sub> (77 ± 7 kJ mol<sup>-1</sup>), and methanol (81 ± 9 kJ mol<sup>-1</sup>). In addition, the production of CO was promoted by the encapsulated water. These results also suggest a mixed-potential-driven mechanism for the synthesis of ethanol.
Authors
- Ryuichi Saito (ORCID: https://orcid.org/0000-0001-5408-2150)
- Bappi Paul (ORCID: https://orcid.org/0000-0001-6845-1340)
- Satoshi Hinokuma (ORCID: https://orcid.org/0000-0002-1764-5089)
- Kotaro Takeyasu (ORCID: https://orcid.org/0000-0002-4472-6992)
- Junji Nakamura (ORCID: https://orcid.org/0000-0002-2837-0535)
- Nuning Anugrah Putri Namari
- Mo Yan (ORCID: https://orcid.org/0009-0008-4465-7342)
Institutions
- University of Tsukuba (JP)
- Hokkaido University (JP)
- Tsukuba University of Technology (JP)
- Fukuoka International University (JP)
- National Institute of Advanced Industrial Science and Technology (JP)
Publication Details
- Journal
- Chemistry - An Asian Journal
- Published
- 2025-11-14
- DOI
- https://doi.org/10.1002/asia.202500862
- Citations
- 1
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.36