Integrated system for electrolyte recovery, product separation, and CO2 capture in CO2 reduction
Challenges in CO<sub>2</sub> capture, CO<sub>2</sub> crossover, product separation, and electrolyte recovery hinder electrocatalytic CO<sub>2</sub> reduction (CO<sub>2</sub>R). Here, we present an integrated electrochemical recovery and separation system (ERSS) with an ion separation module (ISM) between the anode and cathode of a water electrolysis system. During ERSS operation, protons from the anolyte flow through the anodic cation exchange membrane (CEM) into the ISM, acidifying the CO<sub>2</sub>R effluent electrolyte. Cations like K<sup>+</sup> in the ISM flow through the cathodic CEM into the catholyte to balance the OH<sup>-</sup> ions from hydrogen evolution. ERSS recycles electrolyte-adsorbed CO<sub>2</sub>, recovers KOH with a 94.0% K<sup>+</sup> yield, and achieves an 86.2% separation efficiency for CO<sub>2</sub>R products. The recovered KOH can capture CO<sub>2</sub> from air or flue gas or be utilized as a CO<sub>2</sub>R electrolyte, closing the CO<sub>2</sub> capture, conversion, and utilization loop. Compared to the conventional acid-base neutralization process, ERSS saves $119.76 per ton of KOH recovered and is applicable to other aqueous alkaline electrosynthesis reactions.
Authors
- Chengyi Hu (ORCID: https://orcid.org/0000-0002-7962-2034)
- Guangxu Chen (ORCID: https://orcid.org/0000-0002-8670-4708)
- Pingyong Sun
- Nanfeng Zheng (ORCID: https://orcid.org/0000-0001-9879-4790)
- An Pei (ORCID: https://orcid.org/0000-0002-5000-6414)
- Zhaoxi Chen (ORCID: https://orcid.org/0000-0001-8598-152X)
- Peng Wang (ORCID: https://orcid.org/0000-0003-0444-2247)
- Xue Wang (ORCID: https://orcid.org/0000-0002-6298-1858)
Institutions
- City University of Hong Kong (HK)
- Tan Kah Kee Innovation Laboratory (CN)
- Collaborative Innovation Center of Chemistry for Energy Materials (CN)
- State Key Laboratory of Luminescent Materials and Devices
- South China University of Technology (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-01-16
- DOI
- https://doi.org/10.1038/s41467-025-56111-6
- Citations
- 33
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 11.99
Funders
- City University of Hong Kong
- National Natural Science Foundation of China
- Natural Science Foundation of Guangdong Province