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Photoelectrochemical study of hydrothermally grown vertically aligned rutile TiO2 nanorods
•TiO2 nanorods (NRs) were grown using seed less hydrothermal process.•Nanorods are highly crystalline with rutile phase grown along (001) direction.•The optical band gap of the nanorods was found to be 3.19 eV.•Photoelectrochemical (PEC) properties of TiO2 NRs has been investigated in details.•Charg...
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Published in: | Chemical physics 2022-09, Vol.561, p.111609, Article 111609 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •TiO2 nanorods (NRs) were grown using seed less hydrothermal process.•Nanorods are highly crystalline with rutile phase grown along (001) direction.•The optical band gap of the nanorods was found to be 3.19 eV.•Photoelectrochemical (PEC) properties of TiO2 NRs has been investigated in details.•Charge transport mechanism at nanorods-electrolyte interface has been explored.
Vertically oriented TiO2 nanorods (NRs) were grown on FTO coated glass substrate using a hydrothermal process without any seed layer. The morphology and crystallinity of the nanorods were analyzed using SEM, TEM, XRD and Raman spectroscopy. The growth mechanism of the TiO2 nanorods has been discussed. The chemical bonds were studied using XPS study. The PEC properties of the TiO2 NRs were investigated in detail. TiO2 NRs photoanode demonstrated photosensing behaviour with an ON/OFF ratio of ∼96.2 and photoconversion efficiency of ∼0.72%. The incident-photon-to-current conversion efficiency (IPCE) at an incident wavelength of 360 nm was ∼31.6%. The carrier decay life time was estimated from the photovoltage decay profile. The carrier concentration, flat band voltage, Debye length and depletion width at the TiO2 NRs/electrolyte interface were estimated from the Mott-Schottky (M−S) plot. The charge transport mechanism at the semiconductor/electrolyte interface was explored from the electrochemical impedance measurements. |
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ISSN: | 0301-0104 |
DOI: | 10.1016/j.chemphys.2022.111609 |