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