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Strategy for realizing ratiometric optical thermometry via efficient Tb3+-Mn2+ energy transfer in novel apatite-type phosphor Ca9Tb(PO4)5(SiO4)F2.

Authors :
Liu, Haikun
Mei, Lefu
Liao, Libing
Zhang, Yuanyuan
Guo, Qingfeng
Zhou, Tianshuai
Wang, Yongjie
Li, Li
Source :
Journal of Alloys & Compounds. Jan2019, Vol. 770, p1237-1243. 7p.
Publication Year :
2019

Abstract

Abstract The novel apatite-type phosphor Ca 9 Tb(PO 4) 5 (SiO 4)F 2 :Mn2+ (CTPSF:Mn2+) has been successfully synthesized and it demonstrated a potential for optical thermometry. The energy transfer process between Tb3+ and Mn2+ was of resonant type via a dipole-dipole mechanism based on the Inokuti–Hirayama theoretical model, and the energy transfer (ET) efficiency and ET rate were estimated. In view of the energy transfer behavior, a strategy, involving the use of Tb3+ and Mn2+ dual-emitting centers with different thermal quenching behavior, has been developed to achieve temperature sensitivity and good signal discrimination. The temperature dependence of the fluorescence intensity ratios (FIR) for the dual-emission bands peaking at 548 and 595 nm was studied in the range of 298–573 K under excitation of 377 nm ultraviolet light and the maximum relative sensitivity was approximately 1.92% K−1 at 423 K. It is expected that this preliminary study will provide an important advance in exploring novel ratiometric optical thermometry. Highlights • Novel apatite-type phosphor Ca 9 Tb(PO 4) 5 (SiO 4)F 2 was synthesized. • Energy transfer mechanism is estimated based on Inokuti–Hirayama model. • Non-contact thermometry was developed with a new inorganic material. • The maximum S r of the as-prepared phosphor was as high as 1.92% K−1. • This work provides an insight to design ratiometric optical thermometry. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
770
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
132487528
Full Text :
https://doi.org/10.1016/j.jallcom.2018.08.167