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Interfacial carbon-regulated charge transfer and ROS evolution in Ag3PO4 for enhanced photo-persulfate activation.
Jiaxin Li1, Chunmu Yu2, Yu Zhou3
1School of Environment and Chemical Engineering, Foshan University, Foshan, 528225, China.
Biochar-supported silver phosphate (BC/Ag3PO4) composites enhance photocatalysis for tetracycline degradation. This biochar composite improves charge transfer and reactive oxygen species generation, boosting efficiency and stability in environmental remediation.
Area of Science:
- Environmental Science and Engineering
- Materials Science
- Catalysis
Background:
- Conventional silver phosphate (Ag3PO4) photocatalysts exhibit limitations due to photocorrosion and inefficient reactive oxygen species (ROS) evolution.
- Tetracycline (TC) is a persistent organic pollutant requiring effective degradation strategies.
Purpose of the Study:
- To construct a biochar-supported Ag3PO4 (BC/Ag3PO4) composite to improve interfacial charge transfer and ROS evolution.
- To investigate the synergistic effect of the BC/Ag3PO4 composite in a photo-peroxydisulfate (photo-PS) system for tetracycline degradation.
- To elucidate the underlying mechanisms of enhanced degradation and catalyst stability.
Main Methods:
- Synthesis of biochar-supported Ag3PO4 (BC/Ag3PO4) composite.
- Evaluation of the BC/Ag3PO4 composite in a coupled photo-peroxydisulfate (photo-PS) system for tetracycline degradation.
- Mechanistic studies involving interfacial electron transfer, ROS generation, and catalyst stability assessment.
Main Results:
- The BC/Ag3PO4 composite demonstrated a significant synergistic enhancement in TC degradation, with a rate constant 6.61- and 12.92-fold higher than individual photocatalysis and PS systems, respectively.
- Biochar (BC) acted as an interfacial electron mediator and adsorption regulator, facilitating electron redistribution and promoting PS activation, leading to a hybrid ROS microenvironment dominated by OH• and SO4•−.
- The composite system suppressed Ag3PO4 photocorrosion and maintained over 92.66% catalytic activity after five cycles, while accelerating TC degradation and directing it to less toxic pathways.
Conclusions:
- The BC/Ag3PO4 composite effectively reconfigures interfacial charge transfer and ROS evolution in the photo-PS system, leading to superior TC degradation efficiency and catalyst stability.
- The interface-driven strategy provides mechanistic insights for designing advanced carbon-based semiconductor composites for environmental remediation.
- This approach couples high degradation efficiency with detoxification, offering a promising solution for treating organic pollutants.
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