Integrating S-scheme photocatalysis with tandem carbonylation: A green and scalable strategy for CO<sub>2</sub> valorization.
basic_science · Level V
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- Record sourced from PubMed, PMID 40715067.
- Also identified by DOI 10.1038/s41467-025-60961-5 and PMC identifier 12296732.
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Abstract
The rapid increase in atmospheric CO<sub>2</sub> levels due to industrialization underscores the urgent need for innovative carbon valorization strategies. Photocatalytic CO<sub>2</sub> reduction presents a sustainable solution; however, conventional systems suffer from inefficient charge separation and limited product applicability. Herein, a green and scalable tandem strategy is developed by integrating S-scheme photocatalysis with palladium-catalyzed carbonylation. A rationally designed CeO<sub>2</sub>/Bi<sub>2</sub>S<sub>3</sub> heterojunction leverages its hierarchical structure, broad visible-light absorption, oxygen-vacancy-mediated charge dynamics, and the S-scheme charge transfer mechanism to achieve highly efficient photocatalytic CO<sub>2</sub>-to-CO conversion (14.05 mmol g<sup>-1</sup>, 98% selectivity). The generated CO is directly utilized in a subsequent carbonylation reaction under mild conditions, yielding high-value amides with near-quantitative CO utilization. This integrated approach eliminates the risks of CO handling and enhances economic viability, providing a direct and effective route for converting CO<sub>2</sub> into fine chemicals. By bridging photocatalysis with industrial catalysis, this work advances sustainable carbon recycling technologies and opens avenues for the development of efficient CO<sub>2</sub> conversion systems.