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Solar-driven photocatalysis using a new ternary g-C3N4/AgCl/FeOCl heterojunction: Synthesis, characterization, and
Débora F S Morais1, Marcio D Teodoro2, Fabiana V Motta1
1LSQM, Laboratory of Chemical Synthesis of Materials, Department of Materials Engineering, Federal University of Rio Grande do Norte, UFRN, P.O. Box 1524, Natal, RN, Brazil.
A novel g-C3N4/AgCl/FeOCl (AFxCN) heterojunction was synthesized to enhance photocatalytic degradation of organic pollutants. This material effectively suppressed electron-hole recombination, showing high efficiency and stability under solar irradiation.
Area of Science:
- Materials Science
- Environmental Chemistry
- Photocatalysis
Background:
- Iron oxychloride (FeOCl) shows promise as a photocatalyst due to its narrow bandgap and stability.
- Photocatalytic efficiency is often limited by rapid electron-hole recombination in semiconductor materials.
- Developing efficient heterojunctions is crucial for overcoming these limitations in pollutant degradation.
Purpose of the Study:
- To synthesize a novel ternary heterojunction, g-C3N4/AgCl/FeOCl (AFxCN), for improved photocatalytic applications.
- To investigate the suppression of photogenerated carrier recombination in the heterojunction.
- To evaluate the photocatalytic efficiency and stability of the synthesized material against various organic pollutants.
Main Methods:
- Combined calcination and coprecipitation methods were employed for heterojunction synthesis.
- Structural, morphological, and optical characterizations (XRD, PL, photocurrent, EIS) were performed.
- Photocatalytic degradation experiments were conducted under solar irradiation using Malachite Green, Rhodamine B, Methyl Orange, Levofloxacin, and Phenol.
Main Results:
- Successful formation of the g-C3N4/AgCl/FeOCl heterojunction was confirmed.
- The heterostructure demonstrated efficient separation of photogenerated charges, indicated by PL, photocurrent, and EIS analyses.
- Over 70% degradation of diverse organic pollutants was achieved within 30 minutes, with excellent photostability over five cycles.
- XRD analysis revealed the in-situ formation of metallic Ag, transforming the material to g-C3N4/Ag@AgCl/FeOCl.
Conclusions:
- The g-C3N4/AgCl/FeOCl heterojunction effectively enhances photocatalytic activity by suppressing charge recombination.
- The material exhibits excellent degradation efficiency and stability for a range of organic contaminants under solar light.
- A Type-I/S-scheme conjugated heterojunction mechanism is proposed for the g-C3N4/Ag@AgCl/FeOCl system.
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