Loading…

Room temperature photoluminescence of anatase and rutile TiO2 powders

The optical absorption and photoluminescence of anatase and rutile TiO2 were studied at room temperature. TiO2 nanocrystalline powders were synthesized in the form of pure anatase or rutile. The samples were characterized by X-ray diffraction, X-ray fluorescence, Raman spectroscopy, optical absorpti...

Full description

Saved in:
Bibliographic Details
Published in:Journal of luminescence 2014-02, Vol.146, p.199-204
Main Authors: Kernazhitsky, L., Shymanovska, V., Gavrilko, T., Naumov, V., Fedorenko, L., Kshnyakin, V., Baran, J.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The optical absorption and photoluminescence of anatase and rutile TiO2 were studied at room temperature. TiO2 nanocrystalline powders were synthesized in the form of pure anatase or rutile. The samples were characterized by X-ray diffraction, X-ray fluorescence, Raman spectroscopy, optical absorption and photoluminescence (PL) methods. The PL spectra were studied under the intensive UV (3.68eV) laser excitation. Some interesting features in the PL spectra including the well-resolved peaks of excitonic and band–band transitions in TiO2 were observed, to our knowledge, for the first time. It is shown that PL bands including peaks at 2.71–2.81eV and its phonon replicas in anatase and rutile TiO2 arise from the excitonic e−−h+ recombination via oxygen vacancies. The excitonic peak at 2.91eV is attributed to the recombination of self-trapped excitons in anatase or free excitons in rutile TiO2. The PL peaks within 3.0–3.3eV in anatase TiO2 are ascribed to indirect allowed transitions due to the band–band e−−h+ recombination. The peaks at 3.03eV and 3.26eV are attributed to the free exciton emission near the fundamental band edge of rutile and anatase TiO2, respectively. The influence of TiO2 crystal structure and calcination temperature on the PL spectra is discussed. •Well-resolved peaks of the exciton PL at room temperature were observed.•The peaks fine structure is caused by strong exciton–phonon interaction under laser excitation.•The PL intensity in anatase TiO2 powders increases when the specific surface area increases.•The PL intensity in rutile TiO2 powders depends on several competing factors.
ISSN:0022-2313
1872-7883
DOI:10.1016/j.jlumin.2013.09.068