Accelerated Solar-Driven Polyolefin Degradation via Self-Activated Hydroxy-Rich ZnIn<sub>2</sub>S<sub>4</sub>.
basic_science · Level V
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- Record sourced from PubMed, PMID 39225501.
- Also identified by DOI 10.1021/acs.nanolett.4c03067.
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Abstract
Degradation of polyolefin (PE) plastic by a traditional chemical method requires a high pressure and a high temperature but generates complex products. Here, sulfur vacancy-rich ZnIn<sub>2</sub>S<sub>4</sub> and hydroxy-rich ZnIn<sub>2</sub>S<sub>4</sub> were rationally fabricated to realize photocatalytic degradation of PE in an aqueous solution under mild conditions. The results reveal that the optimized photocatalyst could degrade PE into CO<sub>2</sub> and CO, and PE had a weight loss of 84.5% after reaction for 60 h. Systematic experiments confirm that the synergetic effect of hydroxyl groups and S vacancies contributes to improve the photocatalytic degradation properties of plastic wastes. In-depth investigation illustrates that the active radicals attack (h<sup>+</sup> and •OH) weak spots (C-H and C-C bonds) of the PE chain to form CO<sub>2</sub>, which is further selectively photoreduced to CO. Multimodule synergistic tandem catalysis can further improve the utilization value of plastic wastes; for example, product CO<sub>2</sub>/CO in the plastic degradation process can be converted in situ into HCOOH by coupling with electrocatalytic technology.