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Ellouzi, I.* ; Regraguy, B.* ; El Hajjaji, S.* ; Harir, M. ; Schmitt-Kopplin, P. ; Lachheb, H.* ; Laânab, L.*

Synthesis of Fe-doped TiO2 with improved photocatalytic properties under Vis-L irradiation.

Iranian J. Catal. 12, 283-293 (2022)
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Fe-doped TiO2 nanoparticles were successfully synthesized by the coprecipitation method. TiO2 was doped with a different molar ratio of iron amounts, namely 0.1% and 0.2%. An undoped TiO2 was also prepared for comparison. X-ray diffraction (XRD), transmission electron microscopy (TEM) and UV-visible diffuse reflectance spectroscopy techniques were used to characterize the as-synthesized nanoparticles. The XRD spectra revealed that the photocatalysts were mostly in a well-crystallized anatase phase. Optical properties of the powders shifted from UV to the beginning of the visible light (Vis-L) region. Absorption edge wavelengths between 392 and 380 nm were obtained for the Fe-doped TiO2 and TiO2-P25, corresponding to band gap energies between 3.17 and 3.26 eV. TEM images showed homogeneity with a certain degree of agglomeration for all the samples. The photocatalytic efficiency of the as-synthesized Fe-doped TiO2 nanoparticles was performed using azo dye methyl orange (MO) in an aqueous solution under Vis-L irradiation. The photocatalytic results showed that Fe-doped TiO2 nanoparticles effectively degrade MO under Vis-L excitation and follow pseudo-first order kinetics. Besides, kinetic comparison showed that pure TiO2 is less efficient than 0.1% and 0.2% Fe-doped TiO2 because they exhibit unequaled efficiency. Moreover, the photocatalyst at 0.2% Fe-doped TiO2 molar ratio revealed the highest photocatalytic efficiency, which was 4.2 times higher compared to pure TiO2. Different amounts of Fe induced different increases in the apparent first-order rate constant of the photocatalytic process.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Coprecipitation ; Iron ; Mo ; Photocatalytic Degradation ; Titanium Dioxide
ISSN (print) / ISBN 2252-0236
e-ISSN 2252-0236
Quellenangaben Volume: 12, Issue: 3, Pages: 283-293 Article Number: , Supplement: ,
Publisher Islamic Azad University
Non-patent literature Publications
Reviewing status Peer reviewed