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Study on the photoelectrocatalytic activity of reduced TiO2 nanotube films for removal of methyl orange
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Abstract
The reduced TiO2 film on which a photoelectrocatalytic (PEC) process had occurred was created from TiO2 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 TiO2 nanotube film electrode had better photoelectrochemical activities than pristine TiO2 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 TiO2 achieving 7.3 mA‧cm−2, indicating more effective charge separation and transport. The degradation of methyl orange (MO) on pristine TiO2 and reduced TiO2 electrodes was carried out in electrocatalytic (EC) and PEC conditions. The PEC process on the reduced TiO2 electrode had the highest MO processing efficiency (98.4%), and the EC process for MO removal on reduced TiO2 had higher efficiency (95.1%) than the PEC process on pristine TiO2 (89.2%).
Walter de Gruyter GmbH
Title: Study on the photoelectrocatalytic activity of reduced TiO2 nanotube films for removal of methyl orange
Description:
Abstract
The reduced TiO2 film on which a photoelectrocatalytic (PEC) process had occurred was created from TiO2 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 TiO2 nanotube film electrode had better photoelectrochemical activities than pristine TiO2 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 TiO2 achieving 7.
3 mA‧cm−2, indicating more effective charge separation and transport.
The degradation of methyl orange (MO) on pristine TiO2 and reduced TiO2 electrodes was carried out in electrocatalytic (EC) and PEC conditions.
The PEC process on the reduced TiO2 electrode had the highest MO processing efficiency (98.
4%), and the EC process for MO removal on reduced TiO2 had higher efficiency (95.
1%) than the PEC process on pristine TiO2 (89.
2%).
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