Electrochemical Oxidation Strategy for Integrated CO <sub>2</sub> Capture and Conversion
The sequential CO 2 capture and conversion suffer from substantial energy penalties associated with CO 2 recovery. While direct electrochemical (bi)carbonate reduction circumvents this energy-intensive step, it still faces several limitations, including low carbon utilization efficiency, cumbersome product separation, and reliance on the anodic oxygen evolution reaction─a process hampered by slow kinetics and limited economic value. Herein, we present an electrochemical oxidation strategy that directly employs a CO 2 -captured NaOH solution─rich in (bi)carbonate ions─as the electrolyte. In this system, (bi)carbonate-mediated two-electron water oxidation reaction takes place, enabling the in situ generation of H 2 O 2 . Following electrolysis, Na 2 CO 3 ·1.5H 2 O 2, a solid crystalline adduct of Na 2 CO 3 and H 2 O 2, was readily separated from the electrolyte, thereby fixing CO 2 into a storable and value-added product. This integrated approach eliminates the need for energy-intensive CO 2 recovery, offering a streamlined route to convert captured CO 2 into easily isolable, high-value chemicals.
Authors
- Xin Lian (ORCID: https://orcid.org/0000-0003-2107-0641)
- Shanshan Wang (ORCID: https://orcid.org/0000-0003-3750-6737)
- Wenlong Guo (ORCID: https://orcid.org/0000-0003-0551-6711)
- Yun Zhou (ORCID: https://orcid.org/0000-0003-3926-9405)
- Xuanjun Shen
- Shirui Xiao
- Demei Lai
Institutions
- Chongqing Normal University (CN)
- Chongqing University of Science and Technology (CN)
- Green Chemistry (PL)
Publication Details
- Journal
- Langmuir
- Published
- 2026-07-02
- DOI
- https://doi.org/10.1021/acs.langmuir.6c01829
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Natural Science Foundation of Chongqing
- Chongqing Municipal Education Commission