Luminescence Thermometry via Multiparameter Sensing in YV1-xPxO4:Eu3+, Er3

Yixuan Ma, Xiaopeng Zhou, Jiapeng Wu, Zhijie Dong, Lizhi Cui, Yuhua Wang*, Andries Meijerink*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Luminescence thermometry is a remote temperature sensing technique that utilizes temperature-dependent luminescence properties. Lanthanide-doped materials with two thermally coupled emitting levels displaying a variation in luminescence intensity ratio (LIR) with temperature have been successfully explored to design sensitive luminescent thermometers. However, the low absorption strength of lanthanide parity-forbidden 4fn → 4fn transitions reduces the brightness. Also, this Boltzmann-type thermometer is only sensitive within a limited temperature range. To address these issues, we report here YV1-xPxO4:Eu3+, Er3+ as a luminescent thermometer. This material utilizes the sensitized emission of Ln3+ by strong and broad vanadate charge transfer absorption and has a wide and tunable optimum temperature range by controlling the thermal quenching of Eu3+ emission through a variation of x. The new temperature probe offers a single material with multiple temperature-dependent luminescence properties, viz. the LIR of 2H11/2/4S3/2 emission of Er3+, the LIR of the integrated Er3+ and Eu3+ emission intensities, and the Eu3+ emission lifetime. Both micro- and nanocrystalline temperature probes are reported to achieve relative sensitivities (Sr) from ∼0.5%/K to over 5%/K in a wide temperature range of 300-873 K. To demonstrate practical applicability, the luminescent thermometer was applied to in situ chip temperature detection revealing temperature accuracies better than 1 K.

Original languageEnglish
Pages (from-to)12925-12936
Number of pages12
JournalJournal of the American Chemical Society
Volume147
Issue number15
DOIs
Publication statusPublished - 16 Apr 2025

Bibliographical note

Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.

Funding

This work was supported by the National Natural Science Foundation of China (No. 52072163). We thank Prof. Qinyuan Zhang and Prof. Dechao Yu for their assistance with the variable temperature spectroscopy testing.

FundersFunder number
National Natural Science Foundation of China52072163

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