Advanced construction of heterostructured InCrO4-TiO2 and its dual properties of greater UV-photocatalytic and antibacterial activity
The development of coupled semiconductor oxides has led to significant advances in photocatalytic functional materials. In this article, we report the preparation of a nano-spherical InCrO 4 -loaded TiO 2 photocatalyst by a simple co-precipitation method. The InCrO 4 -TiO 2 (ICT) nanomaterial was ch...
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Veröffentlicht in: | RSC advances 2015-09, Vol.5 (94), p.77-7713 |
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Sprache: | eng |
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Zusammenfassung: | The development of coupled semiconductor oxides has led to significant advances in photocatalytic functional materials. In this article, we report the preparation of a nano-spherical InCrO
4
-loaded TiO
2
photocatalyst by a simple co-precipitation method. The InCrO
4
-TiO
2
(ICT) nanomaterial was characterized using XRD, SEM with EDX, FT-IR, FT-Raman and PL analysis. The photocatalytic activity of InCrO
4
-TiO
2
was much better than that of TiO
2
and TiO
2
-P25 under UV-light irradiation. InCrO
4
-TiO
2
showed better activity than TiO
2
and TiO
2
-P25 in the degradation of methyl green (MEG), malachite green (MAG) and methylene blue (MB) because it has maximum efficiency at neutral pH = 7 under UV-light irradiation. Among all these dyes, the photodegradation of MEG was the fastest. The mechanism for the photocatalytic activity of the InCrO
4
-loaded TiO
2
nanomaterial has been discussed. The production of hydroxyl radicals on the surface of UV-irradiated photocatalysts was determined by fluorescence technique using coumarin as a probe molecule. The photodegradation of dyes is well described by pseudo first order kinetics and high quantum yield. Furthermore, the antibacterial activity of the TiO
2
and InCrO
4
-TiO
2
materials was investigated against Gram negative
Vibrio cholerae
and Gram positive
Bacillus subtilis
bacterial strains.
Advanced recylable heterostructured InCrO
4
-TiO
2
was prepared by a simple co-precipitation method, and exhibits high UV-photocatalytic activity and antibacterial activity mechanism owing to the behaviour of its electrons and holes. |
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ISSN: | 2046-2069 |
DOI: | 10.1039/c4ra12453g |