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Dual-driven ratiometric luminescence behaviour of Eu2+ and Eu3+ in a single host of SrAl2O4 prepared in ambient atmosphere.

Authors :
Wang, Ziyao
Ma, Guofeng
Xie, Ci'an
Bu, Xiaoya
Mi, Ruiyu
Chen, Jian
Liu, Yangai
Source :
Journal of Alloys & Compounds. Apr2023, Vol. 941, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

Eu2+/Eu3+ co-activated luminescence as a key technology has gradually attracted attention in many research and application fields, including solid-state lighting, printing and dyeing, temperature sensing, etc. Here, by virtue of the unique self-reduction characteristics of Eu3+ in certain host lattices, Eu2+/Eu3+ co-activated luminescent material of SrAl 2 O 4 :Eu2+/3+ with single host lattice was prepared by solid-state reaction in the ambient atmosphere. The phase composition and crystal structure were determined by X-ray powder diffraction and Rietveld refinement. The micromorphology was observed by scanning electron microscope and transmission electron microscope. From the perspective of applied science, the dual-driven luminescence behavior and temperature-sensing properties of the material were studied and discussed. The ratiometric luminescence of Eu2+ and Eu3+ in SrAl 2 O 4 can be regulated by the excitation wavelength from ultraviolet to visible light. The luminescent material shows temperature-sensing performance superior to other similar Eu2+/Eu3+ co-activated luminescent materials, with absolute sensitivity of 0.067 K−1 and relative sensitivity of 1.6% K−1. The development of this luminescent material provides a unique insight for designing novel Eu2+/Eu3+ co-activated luminescent materials for multifunctional applications. [Display omitted] • The SrAl 2 O 4 :Eu2+/3+ phosphor was obtained through the solid-state reaction in ambient air. • The doping site of Eu was determined by Rietveld refinement and bond energy theory. • The dual-driven luminescence behavior of Eu2+ and Eu3+ in SrAl 2 O 4 :Eu2+/3+ was studied. • The SrAl 2 O 4 :Eu2+/3+ phosphor with superior temperature-sensing properties (S a = 0.067 K−1 and S r = 1.6% K−1) was developed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
941
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
161728794
Full Text :
https://doi.org/10.1016/j.jallcom.2023.168912