Simultaneous CO <sub>2</sub> Capture and Conversion From Flue Gas Using Bicarbonate Electrolysis Over a Nickel Single‐Atom Catalyst
Capturing CO<sub>2</sub> from flue gas and converting it electrochemically into valuable chemicals represents an appealing approach to mitigate CO<sub>2</sub> emissions and realize carbon recycling. Currently, these two processes are usually performed sequentially, which is energy-intensive and involves multiple operational steps. Here, a simultaneous route is reported for capturing and electrochemically converting CO<sub>2</sub> from flue gas without interruption, mediated by bicarbonate electrolysis. The electrochemical conversion of bicarbonate solution, catalyzed by a Ni single-atom catalyst, is unaffected by O<sub>2</sub> and residual NO and SO<sub>2</sub> impurities, commonly found in flue gas. This enables the simultaneous capture and conversion of CO<sub>2</sub> from flue gas into CO without the need to remove these gas components. Mechanistic studies reveal that CO<sub>2</sub> from flue gas is first captured by basified electrolyte and then electrochemically converted. The simultaneous system operates stably for at least 120 h, achieving a CO<sub>2</sub> capture and utilization efficiency of 60%, producing >20000 mL of syngas with a H<sub>2</sub>/CO ratio of ≈3, and reducing energy consumption by 25% compared to the sequential route. This simultaneous route exhibits significant advantages, including simplified operation, enhanced stability, and reduced energy consumption, thereby opening a promising avenue for direct valorization of diluted CO<sub>2</sub> in flue gas.
Authors
- Chengyang Yin (ORCID: https://orcid.org/0000-0002-8380-3532)
- Lin Du (ORCID: https://orcid.org/0000-0001-8208-0558)
- Ao‐Chuan Zheng
- Xin‐Ming Hu (ORCID: https://orcid.org/0000-0003-2219-8786)
- Ye‐Bin Zou
Institutions
- Shandong University (CN)
- Aarhus University (DK)
- Novo Nordisk Foundation (DK)
Publication Details
- Journal
- Small
- Published
- 2025-12-03
- DOI
- https://doi.org/10.1002/smll.202509800
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.00