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Published in: Journal of Materials Science: Materials in Electronics 9/2017

01-02-2017

Enhanced optical and photo catalytic properties of V and La co doped TiO2 nanoparticles

Authors: Nasrollah Najibi Ilkhechi, Nader Ghobadi, Mohammad Reza Akbarpour

Published in: Journal of Materials Science: Materials in Electronics | Issue 9/2017

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Abstract

To enhance the visible photo-catalytic activity of TiO2, La/V co-doped TiO2 materials were synthesized through a nonaqueous method of which the purpose was to reduce the aggregation between TiO2 particles. Different samples of La and V co-doped TiO2 nanoparticles were prepared through simple sol–gel synthesis method by using Vanadium(III) chloride as V precursor, Lanthanum(III) chloride heptahydrate as La precursor, and titanium (IV) butoxide (TBT) as titanium precursor. The effects of co-doping content on the structural, optical, and photo-catalytic properties of nanoparticles have been studied by X-ray diffraction (XRD), TEM, SEM and UV–Vis absorption spectroscopy. XRD results suggest that adding impurities has a great effect on the crystallinity and particle size of TiO2. Titania rutile phase formation in ternary system (Ti–La–V) was inhibited by La3+ and promoted by V4+ co-doped TiO2 in high concentration of vanadium and 22.6 mol% anatase composition is retained at 15% vanadium. The photocatalyst activity was evaluated by photocatalytic degradation kinetics of aqueous methylen orange under visible radiation. The results show that the photocatalytic activity of the 10 mol% V and 5 mol% La co-doped TiO2 nanopowders has a larger degradation efficiency than pure TiO2 under visible light.

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Metadata
Title
Enhanced optical and photo catalytic properties of V and La co doped TiO2 nanoparticles
Authors
Nasrollah Najibi Ilkhechi
Nader Ghobadi
Mohammad Reza Akbarpour
Publication date
01-02-2017
Publisher
Springer US
Published in
Journal of Materials Science: Materials in Electronics / Issue 9/2017
Print ISSN: 0957-4522
Electronic ISSN: 1573-482X
DOI
https://doi.org/10.1007/s10854-016-6328-x

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