Luminescence of GdF3:Pr:Yb and YF3:Pr:Yb Solid Solutions Synthesized by Crystallization from the Melt

Spectral and luminescence characteristics of GdF 3 :Pr:Yb and YF 3 :Pr:Yb solid solutions synthesized by crystallization from the melt were investigated. Down-conversion luminescence of Yb 3+ in the region of 2 F 5/2 → 2 F 7/2 transitions with 445-nm excitation was studied. The energy-transfer coeff...

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Published in:Journal of applied spectroscopy Vol. 86; no. 5; pp. 795 - 801
Main Authors: Nizamutdinov, A. S., Kuznetsov, S. V., Konyushkin, V. A., Nakladov, A. N., Madirov, E. I., Voronov, V. V., Khadiev, A. R., Marisov, M. A., Semashko, V. V.
Format: Journal Article
Language:English
Published: New York Springer US 01-11-2019
Springer Nature B.V
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Summary:Spectral and luminescence characteristics of GdF 3 :Pr:Yb and YF 3 :Pr:Yb solid solutions synthesized by crystallization from the melt were investigated. Down-conversion luminescence of Yb 3+ in the region of 2 F 5/2 → 2 F 7/2 transitions with 445-nm excitation was studied. The energy-transfer coefficient from Pr 3+ to Yb 3+ was <80% for concentration ratios Pr/Yb 0.5/10.0 and 1.0/10.0 for GdF 3 and 0.5/10.0 for YF 3 . The absolute values of Pr 3+ and Yb 3+ luminescence quantum yields in the region of the greatest crystalline-silicon photosensitivity were low because of highly efficient nonradiative energy transfer. The quantum yield was <1% for Yb 3+ intrinsic luminescence and <4% for total luminescence in the range 800–1050 nm (for concentration ratio Pr/Yb = 0.5/1.0 in GdF 3 matrix). The low quantum yield was a consequence of the complex energy-exchange pattern between Yb 3+ and Pr 3+ ions, which was largely influenced by the proximity of 1 G 4 and 2 F 5/2 energy states of Pr 3+ and Yb 3+ , respectively, in these matrices. This opened an additional pathway for nonradiative decay of Yb 3+ excited states and enabled cross-relaxation between 3 P 0 → 1 G 4 transitions of Pr 3+ and 2 F 5/2 → 2 F 7/2 transitions of Yb 3+ that increased the lifetime of the Pr 3+ 3 P 0 state.
ISSN:0021-9037
1573-8647
DOI:10.1007/s10812-019-00895-1