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Detoxification of organic pollutants using a double S-scheme TiO2-x/Co3S4-CoS nanocomposites under visible light

  • Maryam Moslemi-Eilanlou
  • , Aziz Habibi-Yangjeh*
  • , Zahra Salmanzadeh-Jamadi
  • , Alireza Khataee
  • *Bu çalışma için yazışmadan sorumlu yazar
  • University of Mohaghegh Ardebili
  • People's Friendship University of Russia

Araştırma sonucu: Dergiye katkıMakalebilirkişi

Özet

The uncontrolled release of antibiotics and organic dyes into aquatic environments has raised serious concerns about human health and natural ecosystems. In this research, a novel ternary heterostructure photocatalyst composed of oxygen–vacancy rich TiO2 (denoted as TiO2-X), Co3S4, and CoS was fabricated using a hydrothermal route to improve the oxidation efficiency of an antibiotic (Tetracycline hydrochloride: TCH) along with four dye pollutants (Malachite green: MG, Fuchsine: FS, Rhodamine B: RhB, and Methylene blue: MB) when exposed to visible light. The TiO2-X/Co3S4–CoS-2 nanocomposite showed better photocatalytic activity than the TiO2-X and Co3S4-CoS photocatalysts against the degradation of FS (99.4% in 120 min), MB (98% in 210 min), RhB (99.3% in 120 min), MG (99% in 150 min) and TCH (99% in 75 min) under visible light. Furthermore, phytotoxicity assessment using lentil seed growth confirmed the biocompatibility of the treated water. This superior performance can be attributed to the synergistic effects of Co3S4–CoS and TiO2-X, efficient charge transfer through a probable double S-scheme mechanism, increased surface area, rapid photocharge transfer, and the generation of active species. Also, the spherical structure of the photocatalyst may enhance the adsorption of pollutants. These findings demonstrate the innovation and high efficiency of the spherical TiO2-X/Co3S4–CoS-2 heterostructures as environmentally friendly, non-toxic, effective, and reusable photocatalysts for the treatment of antibiotic-contaminated water.

Orijinal dilİngilizce
Makale numarası188489
DergiJournal of Alloys and Compounds
Hacim1068
DOI'lar
Yayın durumuYayınlandı - 25 May 2026

Bibliyografik not

Publisher Copyright:
© 2026 Elsevier B.V.

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