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Study on the photoelectrocatalytic activity of reduced TiO 2 nanotube films for removal of methyl orange
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Abstract
The reduced TiO
2
film on which a photoelectrocatalytic (PEC) process had occurred was created from TiO
2
nanotube film electrodes by the electrochemical reduction method. The obtained samples’ structure and morphology were characterized using UV-Vis diffuse reflectance spectroscopy, scanning electron microscopy, high-resolution transmission electron microscopy, photoluminescence, and X-ray diffraction. Cyclic voltammetry, linear sweep voltammetry, electrochemical impedance spectroscopy, chronoamperometry, UV-Vis absorbance spectroscopy, and Mott–Schottky plots were employed to examine the electrochemical and photoelectrochemical activities of the prepared electrodes. The results showed that the optimal conditions of cathodic polarization were a potential of −1.4 V for 60 min. The reduced TiO
2
nanotube film electrode had better photoelectrochemical activities than pristine TiO
2
under UV light due to the higher photocurrent density (13.7 mA‧cm
−2
) at 1.5 V (vs Ag/AgCl, sat. KCl reference electrode) compared to pristine TiO
2
achieving 7.3 mA‧cm
−2
, indicating more effective charge separation and transport. The degradation of methyl orange (MO) on pristine TiO
2
and reduced TiO
2
electrodes was carried out in electrocatalytic (EC) and PEC conditions. The PEC process on the reduced TiO
2
electrode had the highest MO processing efficiency (98.4%), and the EC process for MO removal on reduced TiO
2
had higher efficiency (95.1%) than the PEC process on pristine TiO
2
(89.2%).
Walter de Gruyter GmbH
Title: Study on the photoelectrocatalytic activity of reduced TiO
2
nanotube films for removal of methyl orange
Description:
Abstract
The reduced TiO
2
film on which a photoelectrocatalytic (PEC) process had occurred was created from TiO
2
nanotube film electrodes by the electrochemical reduction method.
The obtained samples’ structure and morphology were characterized using UV-Vis diffuse reflectance spectroscopy, scanning electron microscopy, high-resolution transmission electron microscopy, photoluminescence, and X-ray diffraction.
Cyclic voltammetry, linear sweep voltammetry, electrochemical impedance spectroscopy, chronoamperometry, UV-Vis absorbance spectroscopy, and Mott–Schottky plots were employed to examine the electrochemical and photoelectrochemical activities of the prepared electrodes.
The results showed that the optimal conditions of cathodic polarization were a potential of −1.
4 V for 60 min.
The reduced TiO
2
nanotube film electrode had better photoelectrochemical activities than pristine TiO
2
under UV light due to the higher photocurrent density (13.
7 mA‧cm
−2
) at 1.
5 V (vs Ag/AgCl, sat.
KCl reference electrode) compared to pristine TiO
2
achieving 7.
3 mA‧cm
−2
, indicating more effective charge separation and transport.
The degradation of methyl orange (MO) on pristine TiO
2
and reduced TiO
2
electrodes was carried out in electrocatalytic (EC) and PEC conditions.
The PEC process on the reduced TiO
2
electrode had the highest MO processing efficiency (98.
4%), and the EC process for MO removal on reduced TiO
2
had higher efficiency (95.
1%) than the PEC process on pristine TiO
2
(89.
2%).
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