Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1618115 | Journal of Alloys and Compounds | 2011 | 6 Pages |
Preparation of anatase TiO2 with high themal stability is of great importance for its environmental application. In this work, TiOF2 was first synthesized by a simple microwave-assisted hydrothermal route using tetrabutyl titanate and hydrofluoric acid as precursors at 200 °C for 20 min. Then the resulted precipitates were calcined at different temperatures (300–1000 °C) for 2 h. The as-prepared samples were characterized by X-ray diffraction, Raman spectrum, scanning electron microscopy, N2 adsorption–desorption isotherms and X-ray photoelectron spectroscopy. The photocatalytic activity was evaluated using Brilliant Red X3B, an anionic azo dye, as the target organic molecule under UV light irradiation. The results showed that the prepared TiOF2 exhibited weak or no photocatalytic activity. The phase transformation of TiOF2 to anatase TiO2 occurred at about 300 °C. The prepared anatase TiO2 from TiOF2 showed very high thermal stability and the anatase-to-rutile phase transformation temperature was up to 1000 °C. Fluoride ions played an important role in the improvement of thermal stability of anatase TiO2 by strongly adsorbing on the crystal planes of anatase to stabilize the anatase structure. The 700 °C-calcined sample showed the highest photocatalytic activity due to its relative good crystallization and high specific surface areas.
Graphical abstractThe prepared anatase TiO2 from TiOF2 shows very high thermal stability (up to 1000 °C) and the 700 °C-calcined sample showed the highest photocatalytic activity.Figure optionsDownload full-size imageDownload as PowerPoint slideResearch highlights► TiOF2 was prepared by a simple microwave assisted hydrothermal rout. ► Anatase TiO2 prepared by calcination of TiOF2 shows high thermal stability. ► F− play an important role in the improvement thermal stability of anatase TiO2. ► The 700 °C-calcined sample shows the highest photocatalytic activity.