51. Blue luminescence of SrTiO3 under intense optical excitation
- Author
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Lorenzo Marrucci, Domenico Paparo, Andrea Rubano, U. Scotti di Uccio, F. Miletto Granozio, Rubano, Andrea, D., Paparo, F., Miletto Granozio, SCOTTI DI UCCIO, Umberto, and Marrucci, Lorenzo
- Subjects
Photoluminescence ,Materials science ,Exciton ,General Physics and Astronomy ,FOS: Physical sciences ,Molecular physics ,time-resolved spectroscopy ,oxygen vacancies ,chemistry.chemical_compound ,symbols.namesake ,Condensed Matter::Materials Science ,Condensed Matter - Strongly Correlated Electrons ,perovksite oxide ,Emission spectrum ,Condensed Matter - Materials Science ,Auger effect ,Strongly Correlated Electrons (cond-mat.str-el) ,crystal defect ,Materials Science (cond-mat.mtrl-sci) ,electronic relaxation ,chemistry ,Excited state ,Strontium titanate ,symbols ,blue luminescence ,Luminescence ,Excitation - Abstract
The blue-green photoluminescence emitted by pure and electron-doped strontium titanate under intense pulsed near-ultraviolet excitation is studied experimentally, as a function of excitation intensity and temperature. Both emission spectra and time-resolved decays of the emission are measured and analyzed in the framework of simple phenomenological models. We find an interesting blue-to-green transition occurring for increasing temperatures in pure samples, which is instead absent in doped materials. The luminescence yield and decay rate measured as a function of temperature can be modeled well as standard activated behaviors. The leading electron-hole recombination process taking place in the initial decay is established to be second-order, or bimolecular, in contrast to recent reports favoring a third-order interpretation as an Auger process. The temporal decay of the luminescence can be described well by a model based on two interacting populations of excitations, respectively identified with interacting defect-trapped (possibly forming excitons) and mobile charges. Finally, from the measured doping and sample dependence of the luminescence yield, we conclude that the radiative centers responsible for the luminescence are probably intrinsic structural defects other than bulk oxygen vacancies.
- Published
- 2009