Weiqing Wu , Yurong Xu , Xinyi Lin , Fazheng Huang , Ya-Nan Feng , Lizhen Zhang , Yan Yu , Lingyun Li
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引用次数: 0
Abstract
Fluorescence intensity ratio (FIR)-based optical thermometry, recognized for high reliability and rapid response, has emerged as a promising non-contact temperature sensing technology. This study focuses on enhancing the performance of Er3+/Yb3+ co-doped scheelite-type single crystals (NaY(WO4)2 and NaGd(WO4)2) for wide-range optical temperature sensing. By employing a spontaneous nucleation method, we synthesized single crystals with optimized doping concentrations (1 % Er3+/60 % Yb3+ for NYW and 3 % Er3+/70 % Yb3+ for NGW), achieving intense green upconversion (UC) emissions at 530 nm (2H11/2 → 4I15/2) and 552 nm (4S3/2 → 4I15/2). The single crystals exhibited high Yb3+→Er3+ energy transfer efficiencies of 11.02 % (NYW: 1 % Er3+, 60 % Yb3+) and 20.65 % (NGW: 3 % Er3+, 70 % Yb3+), enabling robust UC luminescence even under harsh conditions (pH = 1/13, 72 h) and thermal shocks (800 °C, 8 cycles). Temperature-dependent FIR analysis of thermally coupled energy levels (2H11/2 and 4S3/2) revealed linear ln(FIR) vs. 1/T relationships, with maximum relative sensitivities of 1.18 % K−1 (NYW) and 1.12 % K−1 (NGW) in 298–578 K. A prototype sensor utilizing NGW: 3 %Er3+, 70 %Yb3+ single crystal demonstrated practical feasibility across 80–780 K, eliminating fiber-optic requirements due to high UC efficiency. These results highlight scheelite-type single crystals as superior candidates for precision optical thermometry in extreme environments.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.