The effect of charge compensation through alkali metal co-doping on the luminescence behaviour of SrAl4O7:Sm3+ phosphor

The effect of charge compensation through alkali metal co-doping on the luminescence behaviour of... A comparative study of the luminescent properties of singly Sm3+-doped and Sm3+,Na+ co-doped strontium aluminates: Sr1−xSmxAl4O7 and Sr1–2xSmxNaxAl4O7 (x = 0.001–0.1), as a function of activator concentration at room and low (77 K, 16 K) temperature is reported. Upon an excitation at 402 nm all samples exhibit intensive orange-red emission due to the characteristic 4f-4f Sm3+ transitions with maximum located at around 598.7 nm. It was found that luminescence properties of both series of materials differ significantly. In SrAl4O7:Sm3+ at least four distinct activator symmetry sites were identified, which is due to presence of charge compensating defects in the crystal lattice and tendency to form Sm pairs. Charge compensation through alkali metal co-doping led to a smaller perturbation of the local environment symmetry of Sm3+ ions and significantly enhanced luminescence intensity. In SrAl4O7:Sm3+,Na+ only two of the four non-equivalent centers of Sm3+ were found. One of them corresponds to isolated Sm3+ ion occupying basically undistorted Sr2+ symmetry site offered by host lattice but the other is associated with Sm3+ ions forming pairs. Analysis of the luminescence decay traces of both types of materials showed a decreasing decay time constant with rising activator concentration what was mainly attributed to cross-relaxation processes between Sm3+ ions. This effect was slightly more pronounced for the Sm3+,Na+ co-doped series due to higher population of Sm3+ pairs. Fitting of the 4G5/2 state fluorescence decay to the Inokuti–Hirayama model indicated different dominant mechanisms of the self-quenching luminescence of Sm3+ in SrAl4O7:Sm3+ and SrAl4O7:Sm3+,Na+, respectively, dipole-quadrupole interaction and dipole–dipole interaction. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Luminescence Elsevier

The effect of charge compensation through alkali metal co-doping on the luminescence behaviour of SrAl4O7:Sm3+ phosphor

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Publisher
Elsevier
Copyright
Copyright © 2018 Elsevier B.V.
ISSN
0022-2313
eISSN
1872-7883
D.O.I.
10.1016/j.jlumin.2018.01.047
Publisher site
See Article on Publisher Site

Abstract

A comparative study of the luminescent properties of singly Sm3+-doped and Sm3+,Na+ co-doped strontium aluminates: Sr1−xSmxAl4O7 and Sr1–2xSmxNaxAl4O7 (x = 0.001–0.1), as a function of activator concentration at room and low (77 K, 16 K) temperature is reported. Upon an excitation at 402 nm all samples exhibit intensive orange-red emission due to the characteristic 4f-4f Sm3+ transitions with maximum located at around 598.7 nm. It was found that luminescence properties of both series of materials differ significantly. In SrAl4O7:Sm3+ at least four distinct activator symmetry sites were identified, which is due to presence of charge compensating defects in the crystal lattice and tendency to form Sm pairs. Charge compensation through alkali metal co-doping led to a smaller perturbation of the local environment symmetry of Sm3+ ions and significantly enhanced luminescence intensity. In SrAl4O7:Sm3+,Na+ only two of the four non-equivalent centers of Sm3+ were found. One of them corresponds to isolated Sm3+ ion occupying basically undistorted Sr2+ symmetry site offered by host lattice but the other is associated with Sm3+ ions forming pairs. Analysis of the luminescence decay traces of both types of materials showed a decreasing decay time constant with rising activator concentration what was mainly attributed to cross-relaxation processes between Sm3+ ions. This effect was slightly more pronounced for the Sm3+,Na+ co-doped series due to higher population of Sm3+ pairs. Fitting of the 4G5/2 state fluorescence decay to the Inokuti–Hirayama model indicated different dominant mechanisms of the self-quenching luminescence of Sm3+ in SrAl4O7:Sm3+ and SrAl4O7:Sm3+,Na+, respectively, dipole-quadrupole interaction and dipole–dipole interaction.

Journal

Journal of LuminescenceElsevier

Published: May 1, 2018

References

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