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AsymmetricAtomic Pt–B Dual-Site Catalyst forEfficient Photoreforming of Waste Polylactic Acid Plastics in Seawater

Figshare 2025
Zongyang Ya (21147321), Mei Li (217363), Dong Xu (21616), Hua Wang (13530), Shengbo Zhang (5952137)

Summary

Researchers developed a carbon nitride-anchored atomically dispersed platinum-boron dual-site catalyst (Pt SA/BCN100) for photoreforming of polylactic acid plastic waste in seawater, finding through experiments and DFT calculations that the hole-rich boron site selectively cleaved C-H and C-C bonds to produce acetic acid while the electron-rich platinum site reduced protons to generate hydrogen.

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 H2 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 H2. As a result, Pt SA/BCN100 exhibits a high H2 evolution rate of 993 μmol gcatal–1 h–1 and an AA production rate of 300 μmol gcatal–1 h–1 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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