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SrY2S4 – a novel host lattice for up-conversion luminescence and high-sensitive optical thermometry.

Authors :
Mei, Tianjian
Wu, Xingyu
Dong, Xinyao
Yin, Xiumei
Chen, Jianan
Luo, Xilian
Tian, Ying
Source :
CrystEngComm. 4/7/2024, Vol. 26 Issue 13, p1829-1836. 8p.
Publication Year :
2024

Abstract

Lanthanide ion-doped up-conversion (UC) luminescent materials are highly coveted for their utility in diverse applications such as anti-counterfeiting, fluorescence labeling, and temperature sensing. Here, we attempt to adopt SrY2S4 as a novel host lattice for UC luminescence and high-sensitive optical thermometry under near-infrared irradiation. The results show that the single Er3+-doped SrY2S4 samples present their main emissions in green and red regions under 1550 and 980 nm excitations, which correspond to the H11/2/4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions of Er3+ ions, respectively. The green to red intensity ratio increases with the Er3+ concentration under both 980 and 1550 nm excitations. The mechanisms of UC luminescence and energy transfer are further systematically investigated by UC spectra and fluorescence decay dynamics. Furthermore, the non-contact temperature sensing performance of the SrY2S4:10%Er3+ sample is explored via employing fluorescence intensity ratio (FIR) technology. At an excitation of 980 nm, the maximum absolute sensitivity (SA) reaches 7.5 × 10−3 K−1 at 480 K. By utilizing a much safer excitation laser of 1550 nm, the maximum SA achieves 8.4 × 10−3 K−1 at 450 K, with a high and stable SA of more than 7.9 × 10−3 K−1 over a broad temperature range of 360–570 K. The relative sensitivity is 1.06% and 1.01% K−1 under 980 and 1550 nm excitations, respectively. These results indicate that the ternary sulfide SrY2S4 can be adopted as a novel host to achieve promising UC luminescence and thermal sensing performance. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14668033
Volume :
26
Issue :
13
Database :
Academic Search Index
Journal :
CrystEngComm
Publication Type :
Academic Journal
Accession number :
176219374
Full Text :
https://doi.org/10.1039/d3ce01284k