Molecular doping of graphitic carbon nitride for enhanced visible light-driven photodegradation of organic contaminants

Utilizing solar energy for photodegradation of organic contaminants is an attractive strategy for environmental remediation. However, the synthesis of photocatalysts for efficient use of solar energy remains a challenge. Herein, we designed and synthesized a hierarchical and porous g-C3N4 (CN) via t...

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Veröffentlicht in:Journal of alloys and compounds 2025-01, Vol.1010, p.177713, Article 177713
Hauptverfasser: Wang, Guowei, Fu, Shuang, Hou, Peng, Li, Yuedong, Cui, Chunxue, Yi, Tonghui, Zhang, Hongguang
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Sprache:eng
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Zusammenfassung:Utilizing solar energy for photodegradation of organic contaminants is an attractive strategy for environmental remediation. However, the synthesis of photocatalysts for efficient use of solar energy remains a challenge. Herein, we designed and synthesized a hierarchical and porous g-C3N4 (CN) via thermal polymerization of 5-amino-1H-tetrazole (ATZ) and melamine molecules. Experimental results demonstrate that the incorporation of electron-deficient ATZ into the CN structure drastically promotes the separation and transport of photoexcited charge carriers, and increases the specific surface area and pore size of the sample. Based on these unique features, the optimal CN-ATZ1 sample exhibited excellent photocatalytic activity with a rate constant of 0.091 min−1 for the degradation of rhodamine B (RhB) under visible light irradiation, which was about 10.71 times higher than that of bulk CN. Radical trapping experiments demonstrate that the superoxide radical (•O2−) is the major active species during the photodegradation process. This study provides a feasible strategy for the design and construction of g-C3N4 photocatalysts with high degradation activity. •5-amino-1H-tetrazole (ATZ) molecule-doped hierarchical and porous g-C3N4 (CN) was prepared.•The rate constant for the degradation of rhodamine B (RhB) under visible light irradiation was 0.091 min−1.•The superoxide radical (•O2−) is the major active species during the photodegradation process.•Electron-deficient ATZ molecules provide efficient charge migration channels for photogenerated charge electron transfer.
ISSN:0925-8388
DOI:10.1016/j.jallcom.2024.177713