Kinetic Study on the Crystal Transformation of Fe-Doped TiO2 via In Situ High-Temperature X-ray Diffraction and Transmission Electron Microscopy

Titanium dioxide (TiO2) is widely used in various major industries owing to its different crystal forms and functions. Therefore, fabricating suitable crystalline TiO2 through reasonable processes is necessary. In this study, Fe-doped TiO2 precursors were prepared via hydrolysis. Further, in situ high-temperature X-ray diffraction and transmission electron microscopy were used to transform the synthesized precursor in its crystal form. The Rietveld full-spectrum fitting method could accurately yield two different crystal forms at instant temperatures. Additionally, the rate relation between the crystal form transformation and reaction conditions was obtained. Results showed that the addition of Fe increased the temperature of phase transition of TiO2 anatase to rutile and accelerated the anatase -> rutile transformation process. Further, crystal phase transition kinetic analysis showed that the phase transition kinetic model of Fe-doped TiO2 matched the Johnson-Mehl-Avrami-Kohnogorov (JMAK) model and that its phase transition was affected by crystal defects. Finally, Fe3+ in Fe-doped TiO2 was reduced to Fe2+ to generate oxygen vacancies, thus promoting the rate of transformation from titanium ore to rutile.

Automated summary

In this study, Fe-doped TiO2 precursors were prepared and analyzed to investigate the effects of Fe doping on the phase transition of TiO2. Results showed that Fe increased the phase transition temperature from anatase to rutile and accelerated the transformation process. Additionally, the crystal phase transition kinetics of Fe-doped TiO2 was found to follow the JMAK model and was influenced by crystal defects.