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Coconut Fiber Decorated with Bismuth Vanadate for Enhanced Photocatalytic Activity

[Image: see text] Bismuth vanadate/coconut fiber (BiVO(4)/CF) composites were synthesized by coprecipitation and calcination methods. All catalysts used in this work were prepared by a simple coprecipitation method and fully characterized by means of XRD, SEM-EDS, PL, BET N(2) adsorption, zeta poten...

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Detalles Bibliográficos
Autores principales: Channei, Duangdao, Rodsawaeng, Natthamon, Jannoey, Panatda, Khanitchaidecha, Wilawan, Nakaruk, Auppatham, Phanichphant, Sukon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928342/
https://www.ncbi.nlm.nih.gov/pubmed/35309448
http://dx.doi.org/10.1021/acsomega.1c07169
Descripción
Sumario:[Image: see text] Bismuth vanadate/coconut fiber (BiVO(4)/CF) composites were synthesized by coprecipitation and calcination methods. All catalysts used in this work were prepared by a simple coprecipitation method and fully characterized by means of XRD, SEM-EDS, PL, BET N(2) adsorption, zeta potential, and UV–vis DRS. Degradation of indigo carmine (IC) under visible light irradiation was tracked by the UV–vis technique. It was documented that XRD patterns of BiVO(4) and BiVO(4)/CF samples retained the monoclinic structure. From SEM, the CF sheets were visualized, covering the surface of BiVO(4) particles. The specific surface area of the synthesized catalysts increased from 1.77 to 24.82 m(2)/g. The shift of absorption edge to a longer wavelength corresponded to a decrease in band gap energy from 2.3 to 2.2 eV. The photocatalytic degradation rate of the BiVO(4)/CF composite was five times higher than that of pristine BiVO(4). Moreover, the photocatalyst can be separated and recycled with little change after the third times recycling. The improved activity of the composite resulted from the combination of the adsorption performance of the substrate CF and the photocatalytic activity of BiVO(4). In addition, the position of the specific mechanism could occur via both the active species of superoxide radical and hydroxyl radical.