An Electron Transfer Mediated Mechanism for Efficient Photoreforming of Waste Plastics Using a Ni<sub>3</sub>S<sub>4</sub>/ZnCdS Heterojunction.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39989159.
- Also identified by DOI 10.1002/adma.202416581 and PMC identifier 11983256.
- Licence recorded as CC BY-NC-ND.
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Abstract
The oxidative degradation of plastics in conjunction with the production of clean hydrogen (H<sub>2</sub>) represents a significant challenge. Herein, a Ni<sub>3</sub>S<sub>4</sub>/ZnCdS heterojunction is rationally synthesized and employed for the efficient production of H<sub>2</sub> and high-selectivity value-added chemicals from waste plastic. By integrating spectroscopic analysis techniques with density functional theory (DFT) calculations, a solely electron transfer-mediated reaction mechanism is confirmed, wherein Ni<sub>3</sub>S<sub>4</sub> extracts electrons from ZnCdS (ZCS) to promote the spatial segregation of photogenerated electrons and holes, which not only facilitates H<sub>2</sub> production but also maintains the high oxidation potential of holes on the ZCS surface, favoring hole-dominated plastic oxidation. Notably, the catalyst exhibited efficient H<sub>2</sub> production rates as high as 27.9 and 17.4 mmol g<sup>-1</sup> h<sup>-1</sup>, along with a selectivity of 94.2% and 78.3% in the liquid product toward pyruvate and acetate production from polylactic acid (PLA) and polyethylene terephthalate (PET), respectively. Additionally, carbon yields of 26.5% for pyruvate and 2.2% for acetate are measured after 9 h of photoreforming, representing the highest values reported to date. Overall, this research presents a promising approach for converting plastic waste into H<sub>2</sub> fuel and high-selectivity valuable chemical products, offering a potential solution to the growing issue of "White Pollution".