Construction of immobilized films photocatalysts with CdS clusters decorated by metal Cd and BiOCl for photocatalytic degradation of tetracycline antibiotics
A kind of CdS/Cd-BiOCl immobilized films photocatalyst was prepared. The optical and physicochemical properties of the CdS/Cd-BiOCl photocatalysts were analysed, and the detailed characterization revealed CdS/Cd-BiOCl films photocatalyst with good charge carrier separation effect. The reusabilities...
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Veröffentlicht in: | Chinese chemical letters 2022-08, Vol.33 (8), p.3705-3708 |
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Sprache: | eng |
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Zusammenfassung: | A kind of CdS/Cd-BiOCl immobilized films photocatalyst was prepared. The optical and physicochemical properties of the CdS/Cd-BiOCl photocatalysts were analysed, and the detailed characterization revealed CdS/Cd-BiOCl films photocatalyst with good charge carrier separation effect. The reusabilities and photocatalytic properties of the samples were studied. The 15%CdS/Cd-BiOCl photocatalyst exhibited superior performance in photocatalytic degradation of tetracycline (TC) and favorable stability under visible light irradiation. As for the photodegradation rate of TC, 15%CdS/Cd-BiOCl exhibited an excellent photodegradation activity, which is 4.06 and 9.53 times higher than that of CdS/Cd and BiOCl, respectively. The results showed that dominant active species are •O2− and •OH radicals during photodegradation. The charge transfer in Z-scheme CdS/Cd-BiOCl films photocatalyst could synchronously generate conduct band (CB) electrons in BiOCl and valence band (VB) holes in CdS, and metal Cd served as electron mediator. This work can be a reference for the design of film photocatalysts and new insight for photodegradating towards contaminants.
[Display omitted] A ternary composite CdS/Cd-BiOCl immobilized films photocatalyst was prepared to photodegradate tetracycline (TC) antibiotics efficiently under visible light irradiation. The Z-scheme CdS/Cd-BiOCl heterojunction highly boosted the migration and separation of the electron-hole pairs and greatly enhanced the photoactivity. |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2021.10.080 |