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Competing roles of defects in SrAl2O4:Eu2+,Dy3+ phosphors detected by luminescence techniques

Published online by Cambridge University Press:  26 May 2016

Y. Wang*
Affiliation:
School of Science, China University of Geosciences, Beijing, 100083, China
M. Cui
Affiliation:
School of Science, China University of Geosciences, Beijing, 100083, China
Y. Zhao
Affiliation:
School of Science, China University of Geosciences, Beijing, 100083, China
Z.G. Xia
Affiliation:
School of Materials Science & Engineering, University of Science and Technology, Beijing, Beijing, 100083, China
A.A. Finch
Affiliation:
Department of Earth & Environmental Sciences, University of St Andrews, Fife, KY16 9AL, UK
P.D. Townsend
Affiliation:
Physics Building, University of Sussex, Brighton, BN1, 9QH, UK
*
a)Address all correspondence to this author. e-mail: [email protected]
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Abstract

Thermoluminescence (TL) and radioluminescence (RL) spectra of the long-lasting phosphorescence of SrA12O4:Eu2+,Dy3+ with A1N addition and commercially used SrA12O4:Eu2+,Dy3+ were compared. Their spectra were slowly recorded over the temperature range from 25 to 673 K (400 °C). A1N offers a higher temperature TL peak, which should lengthen the phosphor lifetime. However, both TL and RL, especially that below room temperature, reveal that there are additional decay paths for the samples of SrA12O4:Eu2+,Dy3+ with A1N additions. These new defect sites reduce the phosphor efficiency. Some speculative models of potential sites are proposed and discussed. In addition, discontinuous intensity changes have been observed for both sample types in TL and RL spectra, which are assigned to the transitions of embedded impurity phases. The justification for this model is explained. Suggestions for future experimentation are also considered.

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Articles
Copyright
Copyright © Materials Research Society 2016 

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