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Development of Bi(2)S(3)/Cu(2)S hetrojuction as an effective photocatalysts for the efficient degradation of antibiotic drug and organic dye

Herein, a Bi(2)S(3)/Cu(2)S was successfully synthesized via a simple one-step wet impregnation process. The compositional behavior and electrical and optical properties of photocatalysts were investigated in detail. Photocatalytic technology has shown great promise in wastewater treatment, splitting...

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Detalles Bibliográficos
Autores principales: Parasuraman, Balaji, Vasudevan, Vasanthakumar, Kandasamy, Bhuvaneswari, Rangaraju, Hariprasath, Thangavelu, Pazhanivel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073619/
https://www.ncbi.nlm.nih.gov/pubmed/37016260
http://dx.doi.org/10.1007/s11356-023-26627-9
Descripción
Sumario:Herein, a Bi(2)S(3)/Cu(2)S was successfully synthesized via a simple one-step wet impregnation process. The compositional behavior and electrical and optical properties of photocatalysts were investigated in detail. Photocatalytic technology has shown great promise in wastewater treatment, splitting water to hydrogen, and converting CO(2) to fuel. Researchers or scientist are attempting to design sulfate-based heterojunction photocatalytic systems in order to develop novel photocatalysts with excellent performance. Photodegradation of methylene blue (MB) dye and tetracycline (TC) drug under visible light irradiation was used to assess the photocatalytic activity of as-prepared samples. As a result, 2:1% wt of Bi(2)S(3)/Cu(2)S heterostructure composite revealed superior visible light degradation performing of MB dye, and TC drug efficiency as 90.2% and 87.5%, respectively. The prepared hybrid photocatalyst has demonstated a potential for use in the photocatalytic degradation of antibiotic durgs and dyes, indicating a promissing future for its application. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11356-023-26627-9.