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Article ? AI-assigned paper type based on the abstract. Classification may not be perfect — flag errors using the feedback button. Tier 2 ? Original research — experimental, observational, or case-control study. Direct primary evidence. Marine & Wildlife Sign in to save

Asymmetric Atomic Pt–B Dual-Site Catalyst for Efficient Photoreforming of Waste Polylactic Acid Plastics in Seawater

ACS Nano 2025 20 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 63 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Shengbo Zhang, Zongyang Ya, Zongyang Ya Mei Li, Hua Wang, Hua Wang, Dong Xu, Hua Wang, Hua Wang, Shengbo Zhang, Hua Wang, Zongyang Ya, Hua Wang, Zongyang Ya

Summary

Researchers developed a new light-powered catalyst that can break down polylactic acid (PLA) plastic waste in seawater, converting it into useful chemicals and hydrogen fuel. The catalyst uses precisely arranged platinum and boron atoms to efficiently drive the chemical reaction. While focused on cleanup technology rather than health effects, this work offers a promising approach to reducing plastic pollution in the ocean before it breaks down into microplastics.

Polymers
Study Type Environmental

Waste plastic has imposed significant burdens on marine ecosystems. Converting plastic into high-value products via photocatalysis is an emerging and promising approach, but its low activity and product selectivity pose great challenges. Herein, we report a carbon nitride-anchored atomically dispersed Pt-B dual-site catalyst (Pt SA/BCN100) for the photoreforming of polylactic acid (PLA) into high-value chemicals and H<sub>2</sub> in seawater. Experiments and DFT calculations reveal that significantly enhanced charge transfer occurs between the Pt site and the B site, and the hole-rich B site can selectively trigger the activation and cleavage of the C-H and C-C bonds of PLA to form acetic acid (AA), while the electron-rich Pt site drives the reduction of H protons to H<sub>2</sub>. As a result, Pt SA/BCN100 exhibits a high H<sub>2</sub> evolution rate of 993 μmol g<sub>catal</sub><sup>-1</sup> h<sup>-1</sup> and an AA production rate of 300 μmol g<sub>catal</sub><sup>-1</sup> h<sup>-1</sup> with a selectivity of over 98%. We also demonstrate the direct photoreforming of g-scale real-world PLA wastes and low concentrations of PLA microplastics in natural seawater. Techno-economic analysis and environmental assessment show that this catalytic system can significantly reduce carbon emissions and has potential commercial value.

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