Repozytorium

The effect of temperature on green and red upconversion emissions of LiYF4:20Yb3+, 1Ho3+ and its application for temperature sensing.

Autorzy

Weichang Li

Lili Hu

Wei Chen

Shiyu Sun

Małgorzata Guzik

Georges Boulon

Rok wydania

2021

Czasopismo

Journal of Alloys and Compounds

Numer woluminu

866

Strony

158813/1-158813/10

DOI

10.1016/j.jallcom.2021.158813

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Optical thermometry is a non-contact temperature detective technique that has high sensitivity and rapid response. In present work, we developed LiYF4:20Yb3+, 1Ho3+ (mol%) micro octahedrons obtained by a modified hydrothermal method. The temperature dependent up-conversion (UC) emission and luminescence decays for LiYF4:20Yb3+, 1Ho3+ under 976 nm LD excitation with various power density were studied systematically in the temperature range from 100 K to 500 K. The green and red UC emissions are sensitive to the sample temperature whereas the excitation power density in the studied temperature ranges plays a negligible role on the red to green UC emissions ratio. The non-contact optical temperature sensing behaviors were investigated based on the fluorescence intensity ratio (FIR) of red (R3 + R4) and green (G3) at temperature from 100 K to 500 K, which are ascribed to non-thermally coupled levels of Ho3+:5F5 and 5F4, respectively. The maximum absolute sensitivity (Sa) of 0.0477 K−1 and maximum relative sensitivity (Sr) of 0.0129 K−1 at the temperature range of 100–500 K based on FIR of (R3 + R4)/G3 were found. The mechanism of temperature effect on UC emission was discussed. The heating and cooling cycle test indicates the high thermal stability of LiYF4:20Yb3+, 1Ho3+. These results imply the LiYF4:20Yb, 1Ho has potential application in ratiometric thermometers and temperature sensing devices.

Słowa kluczowe

LiYF4:Yb3+ , Ho3+ micro-crystal, temperature sensing, Fluorescence intensity ratio

Adres publiczny

http://dx.doi.org/10.1016/j.jallcom.2021.158813

Strona internetowa wydawcy

http://www.elsevier.com

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