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Article 2022 · 33 citations

Fabrication and characterization of Ag- and Cu-doped TiO<sub>2</sub> nanotubes (NTs) by in situ anodization method as an efficient photocatalyst

Zakir, O., Karra, A. Ait, Idouhli, R., Elyaagoubi, M., Khadiri, M., Dikici, Burak, Aityoub, A., Abouelfida, A., Outzourhit, A.

Abstract

In this study, copper (Cu) and silver (Ag)-doped TiO2 nanotubes were fabricated by in situ anodization method to improve their photocatalytic performance. The resulting nanotubes (NTs) were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Raman spectroscopy, and Mott-Schottky analysis. The SEM study shows the formation of NT structure and reveals that the doping does not affect the surface morphology. The XPS analysis proves that a mixture of Ag-0/Ag+ and Cu+/Cu2+ exists simultaneously on the surface of the Ag- and Cu-doped TiO2 NTs, respectively. XRD and Raman spectroscopy analyses show that the doping shifted the anatase and rutile phase transformation and stabilized the anatase phase. The Mott-Schottky measurements demonstrate that the potential of the flat band shifted to negative values by doping. The prepared NTs were evaluated in methylene blue (MB) photodegradation under UV. The results reveal that the doped TiO2 NTs were more efficient than pure TiO2 NTs in the degradation of MB. The Cu-doped TiO2 NTs exhibited excellent degradation efficiency of about 92.61% with a kinetic rat 0.0089 min(-1). Furthermore, the reusability studies showed that the photocatalysts are globally stable and efficient for the degradation of MB.

Keywords
Electrochemical anodization Photocatalysis Photodegradation Nanotubes TiO2 XPS Methylene blue RAY PHOTOELECTRON-SPECTROSCOPY TITANIUM-DIOXIDE METHYLENE-BLUE ANATASE TIO2 RAMAN-SPECTROSCOPY PARTICLE-SIZE DEGRADATION REDUCTION CO2 OXIDATION
WoS Categories
Electrochemistry
Citation
Journal
JOURNAL OF SOLID STATE ELECTROCHEMISTRY
Year
2022
Volume
26
Issue
10
Pages
2247-2260
ISSN
1432-8488
eISSN
1433-0768
DOI
10.1007/s10008-022-05237-4
WoS UID
WOS:000825217600001
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