Issue 87, 2016, Issue in Progress

Hydrothermal synthesis of the novel rutile-mixed anatase TiO2 nanosheets with dominant {001} facets for high photocatalytic activity

Abstract

In this paper, we introduce a process to synthesize a novel photocatalyst called rutile-mixed anatase nanosheets with dominant {001} facets from a hydrothermal route by using a solution mixed with Ti(OC4H9)4, HF, NH4F and H2O. The crystal structure, micrographs, chemical compositions, and photocatalytic property are characterized and evaluated by using an X-ray diffractometer (XRD), high-resolution transmission electron microscope (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-vis spectrophotometer, and fluorescence spectrophotometer. The experimental results reveal that (1) the addition of NH4F played a crucial role, because it not only changes the chemical environment but also make the phase transformation from anatase to rutile. (2) Compared with the regular anatase TiO2 nanosheets with dominant {001} facets, the present novel photocatalyst exhibits a greatly enhanced photocatalyst activity, i.e., its highest level of photocatalytic activity was about four times higher than that of commercial P25 and the regular anatase TiO2 nanosheets with dominant {001} facets. The mechanism is because the formation of the rutile/anatase heterostructure enhances the separation of the photo-generated electrons and holes. It is expected that this novel photocatalyst will provide wide applications in areas of solar cells, hydrogen generation, photocatalytic environmental pollution treatment, etc.

Graphical abstract: Hydrothermal synthesis of the novel rutile-mixed anatase TiO2 nanosheets with dominant {001} facets for high photocatalytic activity

Article information

Article type
Paper
Submitted
11 Jul 2016
Accepted
31 Aug 2016
First published
31 Aug 2016

RSC Adv., 2016,6, 84035-84041

Hydrothermal synthesis of the novel rutile-mixed anatase TiO2 nanosheets with dominant {001} facets for high photocatalytic activity

G. Song, C. Luo, Q. Fu and C. Pan, RSC Adv., 2016, 6, 84035 DOI: 10.1039/C6RA17665H

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