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Controllable luminescence in Eu2+-doped Li2Sr2Al(PO4)3 phosphor via tuning the Eu2+ concentration and codoping Ce3+.

Authors :
Wanjun, Tang
Zhengxi, Huang
Jiaxuan, Liang
Source :
Journal of Alloys & Compounds. Mar2019, Vol. 778, p612-617. 6p.
Publication Year :
2019

Abstract

Abstract In this work, blue-emitting aluminophosphate phosphor, Li 2 Sr 2 Al(PO 4) 3 :Eu2+, was prepared by the solid state reaction. The influence of Eu2+ concentration on the excitation and emission characteristics of Li 2 Sr 2 Al(PO 4) 3 :Eu2+ has been studied using optical spectroscopy techniques. Upon near UV-light excitation, Li 2 Sr 2 Al(PO 4) 3 :Eu2+ generates a blue band peaked at 445 nm, and a violet band centered at 398 nm, which originate from Eu2+ ions occupying two kinds of crystallographic sites: Sr(1)O 8 and Sr(2)O 9 , respectively. The luminescence intensities of Eu1 and Eu2 have the strong dependence on the Eu2+ concentration. The contribution of Eu2+ luminescence from Eu1 becomes dominant with high Eu2+-doping. Li 2 Sr 2 Al(PO 4) 3 doped with high level of Eu2+ exhibits a strong narrow-band blue emission with a full width at half-maximum of about 42 nm. Meanwhile, the Eu2+ emission can be efficiently enhanced by codoping with Ce3+ ions using exclusive excitation into the Eu2+ absorption band. The mechanism of luminescence enhancement caused by Ce3+ ions has been determined. These results indicate that Li 2 Sr 2 Al(PO 4) 3 :Eu2+,Ce3+ phosphor might be competitive as a potential blue-emitting phosphor for white LEDs. Graphical abstract Image 1 Highlights • Blue-emitting Li 2 Sr 2 Al(PO 4) 3 :Eu2+,Ce3+ phosphor has been prepared. • Two type of Eu2+luminescent centers are identified in Li 2 Sr 2 Al(PO 4) 3 host. • The sensitization effect of Ce3+ on the Eu2+ emission has been determined. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
778
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
134048096
Full Text :
https://doi.org/10.1016/j.jallcom.2018.11.204