Combustion synthesis approach for spectral tuning of Eu doped CaAl2O4 phosphors

•We present a facile solution combustion method for engineering the oxidation state of Eu in open-air.•Eu2+ is stabilized in CaAl2O4 without using any reducing atmospheres viz. H2/N2 or CO.•We tune the redox state of Eu (Eu3+→Eu2+) just by changing the F/O chosen.•Influence of fuel content on lumine...

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Published inJournal of alloys and compounds Vol. 589; pp. 596 - 603
Main Authors Hari Krishna, R., Nagabhushana, B.M., Nagabhushana, H., Chakradhar, R.P.S., Suriyamurthy, N., Sivaramakrishna, R., Shivakumara, C., Rao, J.L., Thomas, Tiju
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 15.03.2014
Elsevier
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Summary:•We present a facile solution combustion method for engineering the oxidation state of Eu in open-air.•Eu2+ is stabilized in CaAl2O4 without using any reducing atmospheres viz. H2/N2 or CO.•We tune the redox state of Eu (Eu3+→Eu2+) just by changing the F/O chosen.•Influence of fuel content on luminescence and colorimetric characteristics were explored.•We have discussed the underlying mechanisms for the observed spectral characteristics. Despite being a particularly good emitter, use of divalent Eu has been seriously limited. This is because severe reducing environments or special hosts are needed during synthesis of divalent Eu containing phosphors. In this work we stabilize Eu in its 2+state (in CaAl2O4) using an open-air solution combustion reaction. The impact of fuel (F) to oxidizer (O) molar ratios (F/O=0.5–2.0) on luminescence properties is explored. Chromaticity of Eu:CaAl2O4 depends sensitively on the F/O ratio. In general, higher F/O inhibits Eu3+ and promotes Eu2+ formation, which in turn improves the quality of the blue phosphor. EPR spectra show inhomogeneous broadening effects with the increase in F/O ratio, which suggests that disorder creation is promoted when F/O is increase. This is also confirmed by an increase in emission line width in PL spectra, when F/O is increased.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2013.11.221