New strategy finds bismuth enhances SO2 resistance during catalytic CO oxidation via theoretical calculations and sulfur analysis.
Sulfur‐induced restructuring of active phases has been identified as one of the dominant reasons why the catalysts are quickly deactivated, posing a significant threat on the long‐term use under practical reaction conditions. Three typical strategies have been proposed for designing the SO 2 ‐resistant nanocatalysts. Herein, a new strategy is discovered to preserve the clean PtO x surfaces in SO 2 ‐containing reaction stream, expected to effectively minimize the sulfur‐induced deactivation. In situ CO‐DRIFTS, FT‐IR, Raman, XPS, HAADF‐STEM, sulfur content determination, and DFT are employed to confirm the PtO restructuring behaviors propelled by the bismuth‐promoted S 2– spillover effect. In situ SO 2 ‐DRIFTS and theoretical calculation results reveal that the adsorption and dissociation of SO 2 on the PtO x surfaces are significantly inhibited once the PtO‐Bi 2 S 3 interfaces are formed by migrating the adsorbed S 2– species to the surfaces of Bi 2 O 3 . The bismuth‐induced dynamic restructuring of PtO surfaces allows to dramatically decrease the activity loss for catalytic CO oxidation and maintain the intrinsic activity following the formate pathway during the introduction of SO 2 molecules. These findings provide a new strategy to design the SO 2 ‐resistant nanocatalysts.
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Liu et al. (2025) studied this question.
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