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

被引:64
|
作者
Liu, Haikun [1 ]
Mei, Lefu [1 ]
Liao, Libing [1 ]
Zhang, Yuanyuan [1 ]
Guo, Qingfeng [2 ]
Zhou, Tianshuai [1 ]
Wang, Yongjie [3 ]
Li, Li [3 ,4 ]
机构
[1] China Univ Geosci, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
[2] China Univ Geosci, Sch Gemmol, Beijing 100083, Peoples R China
[3] Polish Acad Sci, Inst Phys, Al Lotnikow 32-46, PL-02668 Warsaw, Poland
[4] Chongqing Univ Posts & Telecommun, Coll Sci, Chongqing 400065, Peoples R China
关键词
Thermometry; Apatite; Energy transfer; Fluorescence intensity ratios; LIGHT-EMITTING PHOSPHOR; UP-CONVERSION PHOSPHOR; LUMINESCENT PROPERTIES; GLASS-CERAMICS; CO; MN2+; RED; NANOCRYSTALS; RELAXATION; COMPOSITE;
D O I
10.1016/j.jallcom.2018.08.167
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The novel apatite-type phosphor Ca9Tb(PO4)(5)(SiO4)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. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1237 / 1243
页数:7
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