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Synthesis and luminescence properties of broad band greenish-yellow emitting LnVO4:Bi3+ and (Ln1, Ln2)VO4:Bi3+ (Ln=La, Gd and Y) as down conversion phosphors

Ln0.97VO4:Bi0.033+ and (Ln10.5, Ln20.5)0.97VO4:Bi0.033+ (where Ln=La, Gd and Y) down conversion (DC) phosphors have been synthesized by a novel co-precipitation technique followed by heat-treatment. The influence of lanthanide host composition on crystal structure, luminescence and pertinent optical...

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Published in:Ceramics international 2013-01, Vol.39 (1), p.701-708
Main Authors: Rambabu, U., Han, Sang-Do
Format: Article
Language:English
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Summary:Ln0.97VO4:Bi0.033+ and (Ln10.5, Ln20.5)0.97VO4:Bi0.033+ (where Ln=La, Gd and Y) down conversion (DC) phosphors have been synthesized by a novel co-precipitation technique followed by heat-treatment. The influence of lanthanide host composition on crystal structure, luminescence and pertinent optical properties have been investigated by various spectroscopic techniques: XRD, SEM, FT-IR and PL. The produced phosphors have exhibited an intense greenish-yellow emission, upon UV-irradiation. A broad band excitation (280–350nm) ascribed to 1S0→3P1 and an intense broad greenish-yellow emission band (400–700nm) attributed to 3P1→1S0 transition, owing to Bi3+ ions have been observed. PL spectra revealed that the phosphors with Gd – containing host has exhibited a better luminescence among the others. The luminescence intensity sequence in descending order was as follows: GdVO4→(Gd, Y)VO4→(La, Gd)VO4→(La, Y)VO4→YVO4→LaVO4: Bi3+. These phosphors can efficiently convert the UV-photons in a broad range from 280–350nm of feckless UV-rays into the absorbable visible emission for c-Si solar cells, based on the spectral matching phenomena. In view of the better fluorescence and pertinent optical properties, the phosphor with composition Gd0.97VO4: Bi0.033+ is a suggestible sought UV-absorbing spectral converter, in its thin transparent DC form for c-Si solar cells for better harvesting the solar energy.
ISSN:0272-8842
1873-3956
DOI:10.1016/j.ceramint.2012.06.081