Electrochemical CO <sub>2</sub> Reduction in the Presence of SO <sub>2</sub> Impurities on a Nitrogen-Doped Carbon Electrocatalyst
Electrochemical CO<sub>2</sub> reduction to CO offers a sustainable route for converting CO<sub>2</sub> into value-added chemicals and fuels. However, CO<sub>2</sub> streams derived from industrial sources often contain SO<sub>2</sub> impurities that severely poison conventional metal-based catalysts. Here, we report a nitrogen-doped carbon catalyst that exhibits pronounced tolerance and stability for CO<sub>2</sub>-to-CO conversion in the presence of SO<sub>2</sub> (100-10,000 ppm). The catalyst maintains over 90% Faradaic efficiency toward CO during 8 h of electrolysis at -1.0 V vs RHE with 100 ppm of SO<sub>2</sub>, whereas Ag foil electrodes undergo rapid deactivation. Density functional theory calculations combined with surface analyses indicate that weak SO<sub>2</sub> adsorption and the absence of stable sulfur accumulation on nitrogen-doped carbon strengthen its resistance to impurity-induced deactivation, in contrast to Ag catalysts that form Ag<sub>2</sub>S. Gas-fed tests in a membrane electrode assembly (MEA) electrolyzer further confirm that nitrogen-doped carbon sustains high CO selectivity at elevated current densities, while Ag nanoparticles suffer irreversible sulfur poisoning. These results demonstrate that nitrogen-doped carbon is intrinsically resistant to SO<sub>2</sub>-induced deactivation and highlight its potential as a robust catalyst for CO<sub>2</sub> electroreduction under impurity-containing conditions.
Authors
- Othonas A. Moultos (ORCID: https://orcid.org/0000-0001-7477-9684)
- Shilong Fu
- Ruud Kortlever (ORCID: https://orcid.org/0000-0001-9412-7480)
- M. Li
- Bowen Sha
- Thijs J. H. Vlugt
- Asvin Sajeev
- Wiebren de Jong
Institutions
- Delft University of Technology (NL)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-02-04
- DOI
- https://doi.org/10.1021/jacs.5c11790
- Primary Topic
- CO2 Reduction Techniques and Catalysts
- Type
- article
- Field-Weighted Citation Impact
- 0.00