4.7 Article

The structural, optical, magnetic and photocatalytic properties of transition metal ions doped TiO2 nanoparticles

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 581, Issue -, Pages 71-78

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2013.07.041

Keywords

Anatase TiO2 nanoparticle; Transition metal ion doping; Hydrothermal processes; Magnetic property; Photocatalytic property

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Metal-ions doped TiO2 (M-TiO2) have been synthesized using a hydrothermal method at 100 degrees C with a post-annealing temperature process at 500 degrees C, including individual Co2+, and Mn2+ ions. Furthermore, effects of these doping metals ions on the crystallization and phase transition of the TiO2 nanoparticles were discussed by XRD, TEM/HRTEM, BET specific surface area (SBET), pore-size distribution by BJH, UV-vis Spectroscopy, photoluminescence (PL), FTIR, VSM as well as photocatalytic measurements. The presence of anatase type structure in TiO2 nanopowders with high crystallinity and high phase stability even after annealing at 500 degrees C substantially indicated that the dopants might inhibit densification and crystallite growth in TiO2 nanophase by providing dissimilar boundaries. Moreover, with a suitable amount (ca. 0.2, 0.3 mol%), the Mn, Co dopants reduces anatase grain size and increases the specific surface area of TiO2 powders. The band gap energy values of Mn2+ and Co2+ ions doped nano-TiO2 were higher than the pure nano-TiO2 and they showed a blue shift to the visible region. Furthermore, the obtained experimental results revealed that all the samples exhibited the paramagnetic behavior at room temperature. The paramagnetic order was increased with increasing the (Mn, Co) content, whereas the coercivity force Hc was decreased. Photocatalytic degradation of methylene blue (MB) under UV lights indicated that the meso-TiO2 exhibited enhanced activity under UV lights. However, photodegradation of the MB under UV light was enhanced with the presence of Mn and Co with TiO2. (C) 2013 Elsevier B. V. All rights reserved.

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