Optical thermometry using efficient upconversion luminescence in Er3+ self-sensitized NaYS2 under multi-wavelength excitation

IF 3.3 3区 物理与天体物理 Q2 OPTICS
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Abstract

Herein, a series of Er3+ self-sensitized NaYS2 phosphors are synthesized by the solid-gas reaction method for a novel upconversion luminescence thermometer. Er3+ possesses abundant excited state energy levels in the near-infrared region, enabling efficient upconversion luminescence by absorbing different near-infrared wavelength light. Compared to 980 nm excitation, the emission intensity is enhanced by nearly an order of magnitude under 1532 nm excitation, which can be attributed to the larger absorption cross-section of 4I13/2 and stronger absorption efficiency for Er3+. Based on the luminescence intensity ratio technique, the optical thermometry behaviors of NaYS2:Er3+ under different wavelength excitation are evaluated by employing the thermally coupled energy levels of 2H11/2/4S3/2. It can be deduced that the excitation wavelength has no significant effect on the temperature sensing parameters. Compared to other typical upconversion luminescence thermometers, NaYS2:Er3+ thermometer exhibits not only excellent sensitivity performance but also high upconversion luminescence efficiency, which is expected to be applied in wide-temperature-range and highly-sensitive temperature sensing.

在多波长激发下,利用 Er3+ 自敏化 NaYS2 中的高效上转换发光进行光学测温
本文采用固气反应法合成了一系列 Er3+ 自敏化 NaYS2 荧光粉,用于新型上转换发光温度计。Er3+ 在近红外区域具有丰富的激发态能级,可通过吸收不同波长的近红外光而实现高效的上转换发光。与 980 nm 激发相比,1532 nm 激发下的发射强度增强了近一个数量级,这可能是由于 4I13/2 的吸收截面更大,Er3+ 的吸收效率更高。基于发光强度比技术,利用 2H11/2/4S3/2 的热耦合能级评估了 NaYS2:Er3+ 在不同波长激发下的光学测温行为。结果表明,激发波长对温度传感参数没有明显影响。与其他典型的上转换发光温度计相比,NaYS2:Er3+ 温度计不仅灵敏度高,而且上转换发光效率也很高,有望应用于宽温范围、高灵敏度的温度传感。
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
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.
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