Electrochemical CO2 reduction demonstrates stability in SO2-impurified environments, suggesting a promising catalyst alternative.
Electrochemical CO₂ reduction to CO offers a sustainable route for converting CO₂ into value-added chemicals and fuels. However, CO₂ streams derived from industrial sources often contain SO₂ impurities that severely poison conventional metal-based catalysts. Here, we report a nitrogen-doped carbon catalyst that exhibits pronounced tolerance and stability for CO₂-to-CO conversion in the presence of SO₂ (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 SO₂, whereas Ag foil electrodes undergo rapid deactivation. Density functional theory calculations combined with surface analyses indicate that weak SO₂ 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 Ag₂S. 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 SO₂-induced deactivation and highlight its potential as a robust catalyst for CO₂ electroreduction under impurity-containing conditions.
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Fu et al. (2026) studied this question.
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