Multiphonon transitions in LaAlO3 doped with rare earth ions
Identifieur interne : 001110 ( Main/Exploration ); précédent : 001109; suivant : 001111Multiphonon transitions in LaAlO3 doped with rare earth ions
Auteurs : Przemysław J. Deren [Pologne] ; Rachid Mahiou [France] ; Philippe Goldner [France]Source :
- Optical materials : (Amsterdam) [ 0925-3467 ] ; 2009.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
From radiative transitions rates in praseodymium, neodymium, erbium, holmium and thulium ions doped LaAlO3 and measured emission decay times multiphonon nonradiative transitions rates WMNR have been calculated. Radiative transition rates were determined in the frame of Judd-Ofelt theory. The data obtained were plotted in the function of energy gap ΔE and fitted by exponential function WMNR = B . exp(-α . ΔE), where B = 1.02 x 109 and α = 3.61 x 10-3. Fitting results show that multiphonon nonradiative transition rates are low comparing to other oxide crystals being similar to those of YAG.
Affiliations:
- France, Pologne
- Auvergne (région administrative), Auvergne-Rhône-Alpes, Île-de-France
- Clermont-Ferrand, Paris
- Université Blaise-Pascal
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Le document en format XML
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<term>Doped materials</term>
<term>Emission spectra</term>
<term>Lanthanum Oxides</term>
<term>Laser materials</term>
<term>Multi-phonon processes</term>
<term>Nonradiative transitions</term>
<term>Optical materials</term>
<term>Radiative transition</term>
<term>Rare earth additions</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Transition radiative</term>
<term>Transition non radiative</term>
<term>Spectre émission</term>
<term>Matériau dopé</term>
<term>Matériau optique</term>
<term>Addition lanthanide</term>
<term>Matériau laser</term>
<term>Processus n phonons</term>
<term>Lanthane Oxyde</term>
<term>Aluminium Oxyde</term>
<term>Al O Y</term>
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<front><div type="abstract" xml:lang="en">From radiative transitions rates in praseodymium, neodymium, erbium, holmium and thulium ions doped LaAlO<sub>3</sub>
and measured emission decay times multiphonon nonradiative transitions rates W<sub>MNR</sub>
have been calculated. Radiative transition rates were determined in the frame of Judd-Ofelt theory. The data obtained were plotted in the function of energy gap ΔE and fitted by exponential function W<sub>MNR</sub>
= B . exp(-α . ΔE), where B = 1.02 x 10<sup>9</sup>
and α = 3.61 x 10<sup>-3</sup>
. Fitting results show that multiphonon nonradiative transition rates are low comparing to other oxide crystals being similar to those of YAG.</div>
</front>
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