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Optimising synthesis conditions for long lasting SrAl2O4 phosphor

B. Faridnia (Chemistry Department, Iran University of Science and Technology, Tehran, Iran)
M.M. Kashani Motlagh (Chemistry Department, Iran University of Science and Technology, Tehran, Iran)
A. Maghsoudipour (Ceramic Department, Materials and Energy Research Center, Karaj, Iran)

Pigment & Resin Technology

ISSN: 0369-9420

Article publication date: 10 July 2007

1109

Abstract

Purpose

To evaluate the effect of flux, activator and co‐activator on solid state synthesis of SrAl2O4: Eu2 + , Dy3 +  phosphor, where boric oxide, europium oxide and dispersium oxide were used, respectively.

Design/methodology/approach

To optimise synthesis condition of long lasting phosphorescence SrAl2O4 phosphor, boric oxide was used as a flux. To improve relative intensity of SrAl2O4: Eu2 +  phosphor, the critical concentration of Eu2 +  was determined. The effect of various concentration of co‐activator on afterglow properties, the effect of Dy3 +  ion on the emission and excitation spectra were examined.

Findings

The SrAl2O4: Eu2 + , Dy3 +  phosphor powders have been synthesised by solid state reaction method. The result of XRD patterns indicated that, addition of 5 mol% B2O3 enhanced the formation of SrAl2O4 at 1,200°C. Investigation on the variation of emission intensity of different phosphors containing different amounts of Eu2 +  revealed that after 6 mol% of Eu2 +  concentration, quenching process occurred. Dy3 +  formed trap levels and results demonstrated that increasing concentration of Dy3 +  up to 5 mol% reduced the relative intensity and increased the decay time.

Originality/value

Using B2O3 as a flux and solid state reaction method for preparation of this phosphor is in good agreement with industrial production and make it economic, because of reduced sintering temperature.

Keywords

Citation

Faridnia, B., Kashani Motlagh, M.M. and Maghsoudipour, A. (2007), "Optimising synthesis conditions for long lasting SrAl2O4 phosphor", Pigment & Resin Technology, Vol. 36 No. 4, pp. 216-223. https://doi.org/10.1108/03699420710761816

Publisher

:

Emerald Group Publishing Limited

Copyright © 2007, Emerald Group Publishing Limited

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