Study on the catalytic activities of g-C3N4@TiO2 hollow microspheres under UV–visible light
TiO 2 and g-C 3 N 4 samples were successfully prepared by simple one-step hydrothermal method and calcination method, respectively. Then, g-C 3 N 4 @TiO 2 hollow microspheres were prepared by simple water bath evaporation method. This work mainly studies the photocatalytic performance of a series of...
Gespeichert in:
Veröffentlicht in: | Journal of materials science. Materials in electronics 2021-02, Vol.32 (4), p.5104-5115 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | TiO
2
and g-C
3
N
4
samples were successfully prepared by simple one-step hydrothermal method and calcination method, respectively. Then, g-C
3
N
4
@TiO
2
hollow microspheres were prepared by simple water bath evaporation method. This work mainly studies the photocatalytic performance of a series of g-C
3
N
4
composite TiO
2
hollow microspheres with different contents. In the experiment, the amount of g-C
3
N
4
was adjusted to obtain the highest photocatalytic activity. Therefore, finding the most suitable amount of g-C
3
N
4
has become the main task of this work. By degrading the catalytic effect of Rhodamine B (RhB) solution, the photocatalytic performance of a series of samples was compared. Finally, it was discovered that when the weight ratio of g-C
3
N
4
to TiO
2
was 15%, the photocatalytic effect of the sample prepared in this way was the best and the sample was recorded as 15% g-C
3
N
4
@TiO
2
composite. The heterostructure of TiO
2
and g-C
3
N
4
was constructed through the synergistic effect, achieving excellent photocatalytic performance to a certain extent. Therefore, the degradation rate of 15% g-C
3
N
4
@TiO
2
composite material is 90.8% within 90 min of UV–visible light irradiation. We further used SEM, TEM, XRD, FT-IR spectroscopy, DRS, XPS and other test methods to characterize the composition, morphology and chemical properties of the composite material. |
---|---|
ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-021-05244-7 |