Original Synthetic Route To Obtain a SrAl2O4 Phosphor by the Molten Salt Method: Insights into the Reaction Mechanism and Enhancement of the Persistent Luminescence

SrAl2O4:Eu2+, Dy3+ has been extensively studied for industrial applications in the luminescent materials field, because of its excellent persistent luminescence properties and chemical stability. Traditionally, this strontium aluminate material is synthesized in bulk form and/or fine powder by the c...

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Published in:Inorganic chemistry Vol. 54; no. 20; pp. 9896 - 9907
Main Authors: Rojas-Hernandez, Rocío Estefanía, Rubio-Marcos, Fernando, Gonçalves, Ricardo Henrique, Rodriguez, Miguel Ángel, Véron, Emmanuel, Allix, Mathieu, Bessada, Catherine, Fernandez, José Francisco
Format: Journal Article
Language:English
Published: United States American Chemical Society 19-10-2015
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Summary:SrAl2O4:Eu2+, Dy3+ has been extensively studied for industrial applications in the luminescent materials field, because of its excellent persistent luminescence properties and chemical stability. Traditionally, this strontium aluminate material is synthesized in bulk form and/or fine powder by the classic solid-state method. Here, we report an original synthetic route, a molten salt assisted process, to obtain highly crystalline SrAl2O4 powder with nanometer-scale crystals. The main advantages of salt addition are the increase of the reaction rate and the significant reduction of the synthesis temperature because of much higher mobility of reactants in the liquid medium than in the solid-state method. In particular, the formation mechanism of SrAl2O4, the role of the salt, and the phase’s evolution have been explored as a function of temperature and time. Phosphorescent powders based on SrAl2O4:Eu2+, Dy3+ with high crystallinity are obtained after 1 h treatment at 900 °C. This work could promote further interest in adopting the molten salt strategy to process high-crystallinity materials with enhanced luminescence to design technologically relevant phosphors.
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ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.5b01656