Continuous electrolytic methanol synthesis from air-captured CO2 at ordinary temperature and pressure
A system for synthesizing methanol (MeOH) from carbon dioxide (CO 2 ) in the air as a feedstock using electrical energy was developed to open a new avenue for atmospheric carbon capture and utilization. This system integrates three processes: direct air capture (DAC), direct carbonate reduction (DCR), and MeOH synthesis (MeS). A mixture of potassium carbonate and potassium bicarbonate aqueous solutions captures CO 2 from the air as carbonate ions. Carbonate ions in the solution are directly reduced electrolytically to carbon monoxide (CO) using a nanoporous gold electrocatalyst. The produced CO is subsequently reduced electrolytically to MeOH using a cobalt phthalocyanine/carbon nanotube electrocatalyst. The system operated stably for 1.5 h, showing continuous CO 2 capture and MeOH synthesis. This demonstrates the feasibility of the DAC-DCR-MeS integrated system operating under ordinary temperature and pressure conditions throughout all the steps. A notable feature of no need for high temperature or high pressure makes the system compatible with time-varying renewable energies including solar energy, which are essential for reducing net CO 2 emissions.
Authors
- Y. Sakamoto (ORCID: https://orcid.org/0000-0001-8636-4697)
- Shintaro Mizuno (ORCID: https://orcid.org/0000-0001-7560-6849)
- Yusaku F. Nishimura (ORCID: https://orcid.org/0000-0002-2672-8732)
- Kazumasa Okamura
- Tsuyoshi Hamaguchi (ORCID: https://orcid.org/0000-0003-4959-6004)
- Yuna Takeno
- Masaoki Iwasaki (ORCID: https://orcid.org/0000-0002-3987-0017)
- Yasuhiko Takeda (ORCID: https://orcid.org/0000-0002-0874-4560)
- Yohsuke Mizutani
- Ryo Hishinuma
Institutions
- Toyota Motor Corporation (Japan) (JP)
- Toyota Central Research and Development Laboratories (Japan) (JP)
Publication Details
- Journal
- Carbon Capture Science & Technology
- Published
- 2025-11-28
- DOI
- https://doi.org/10.1016/j.ccst.2025.100552
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.00