Preparation, characterization and photocatalytic degradation properties of Zn0.5Cd0.5S/SnO2 composites
The Zn 0.5 Cd 0.5 S/SnO 2 composite photocatalyst was synthesized via a hydrothermal method. The crystal phase, micromorphology, optical and photoelectric property as well as surface elements valence were characterized using X-ray diffraction, field emission scanning electron microscope, transmissio...
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Veröffentlicht in: | Journal of materials science. Materials in electronics 2020, Vol.31 (2), p.1585-1593 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The Zn
0.5
Cd
0.5
S/SnO
2
composite photocatalyst was synthesized via a hydrothermal method. The crystal phase, micromorphology, optical and photoelectric property as well as surface elements valence were characterized using X-ray diffraction, field emission scanning electron microscope, transmission electrical microscope, UV–Vis diffuse reflectance spectrometer, electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy, respectively. Tetracycline was used to discuss the photocatalytic properties of the samples under visible light irradiation. Research results indicate that the as-synthesized Zn
0.5
Cd
0.5
S/SnO
2
composite photocatalysts show better photocatalytic performance than that of pure samples. Moreover, the photocatalytic activity of the as-synthesized composites presents first increased and then decreased with increasing the amount of SnO
2
in the composites. When the quality ratio of SnO
2
to Zn
0.5
Cd
0.5
S is 7%, in 60 min, the as-synthesized composites reveal the best photocatalytic degradation efficiency of 92.9%, which is high than 85% of Zn
0.5
Cd
0.5
S and 0% of SnO
2
. This is ascribed of the improvement of the separation efficiency of photo-generated electron–hole pairs and the transmission rate of electrons. Furthermore, the decomposition mechanism of as-synthesized composites for tetracycline was also provided. The holes and superoxide radicals play crucial species in the photocatalytic degradation process. |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-019-02675-1 |