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Efficient energy transfer, multi-colour emitting and temperature sensing behavior of single-phase Tb3+, Eu3+ co-doped strontium fluoride phosphors.

Authors :
Yan, Yu
Tan, YongJun
Li, Dewei
Luan, Fangfei
Guo, Dongcai
Source :
Journal of Luminescence. Jul2019, Vol. 211, p209-217. 9p.
Publication Year :
2019

Abstract

A succession of single-phase SrF 2 : Tb3+, Eu3+ phosphors with adjustable output colour were prepared via chemical co-precipitation technique. The crystal structure, scanning electron microscopy (SEM), photo-luminescence excitation (PLE) spectrum, photo-luminescence emission (PL) spectrum, photo-luminescence decay curve and thermal stability studies were used to analyze systematically the energy transfer (ET) properties in SrF 2 host. SrF 2 :Eu3+ phosphors present an obvious orange fluorescence and SrF 2 :Tb3+ phosphors exhibit the characteristic green fluorescence. The optimal single dopant contents of Eu3+ and Tb3+ are 7 mol% and 6 mol%, respectively. By optical analysis, it can be inferred that Eu3+ and Tb3+ may mainly occupy the reverse symmetric position. Moreover, in the 6 mol%Tb3+, zmol% Eu3+ co-doped SrF 2 samples, the intensity of terbium ions characteristic emission (545 nm) decreases monotonically and europium ions characteristic emission (592 nm) increases monotonously by elevating amounts of Eu3+ contents. Thus the alteration of light output colour from green to yellow and definitively to orange can be observed via appropriately adjusting Eu3+/Tb3+ ratios. ET type was testified in SrF 2 host is a quadrupole-quadrupole mechanism. Additionally, the critical distance of ET from terbium to europium, which was calculated by quenching concentration method, was 10.521 Å. Meanwhile, the SrF 2 : 6 mol% Tb3+, 1 mol% Eu3+ exhibits a good thermal stability, so, it will have potential applications for n-UV w-LEDs. Image 1 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222313
Volume :
211
Database :
Academic Search Index
Journal :
Journal of Luminescence
Publication Type :
Academic Journal
Accession number :
136252721
Full Text :
https://doi.org/10.1016/j.jlumin.2019.03.040