Intrinsic optical bistability and temperature sensing in the Laser–Induced Anti-Stokes broadband white light emission

IF 3.6 3区 物理与天体物理 Q2 OPTICS
Journal of Luminescence Pub Date : 2026-02-01 Epub Date: 2025-11-19 DOI:10.1016/j.jlumin.2025.121655
Talita J.S. Ramos
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Abstract

In this work, we provide a detailed investigation into the underlying mechanisms of laser-induced white light emission (LIWE) and examine the effects of particle size and bulk properties on the optical features of lanthanide sesquioxides. The upconversion emission colour is tunable by changes in sample packing density, laser diode intensity and continuous excitation wavelength at 808 or 980 nm up to 11 kW cm−2. The results demonstrate that the slope for the linear fit for Log ILIWE vs Log PD should not be interpreted as the number of photons in the LIWE process. The temporal dynamics and photoconductivity analysis indicate that multiphoton ionisation and avalanche processes are not involved in LIWE generation. The minor resistance oscillations (within one order of magnitude) over a timescale of seconds, along with photocurrent intensities in the nA, can be attributed to a light-to-heat mechanism induced by laser excitation. The single emitters reported here present intrinsic optical bistability coupled to temperature sensing in a wide range, 972−2542 K, with a high resolution of 0.2 K. The photophysical analysis indicates that there are two optical bistable emissions at low/high laser power densities.

Abstract Image

激光诱导反斯托克斯宽带白光发射的固有光双稳性和温度传感
在这项工作中,我们对激光诱导白光发射(LIWE)的潜在机制进行了详细的研究,并研究了粒度和体积性质对镧系半氧化物光学特性的影响。上转换发射颜色可以通过改变样品包装密度、激光二极管强度和808或980 nm的连续激发波长(高达11 kW cm - 2)来调节。结果表明,Log ILIWE与Log PD线性拟合的斜率不应被解释为LIWE过程中的光子数。时间动力学和光电导率分析表明,LIWE的产生不涉及多光子电离和雪崩过程。微小的电阻振荡(在一个数量级内)在秒的时间尺度上,随着nA中的光电流强度,可以归因于激光激发引起的光-热机制。本文报道的单发射器在972 ~ 2542 K的宽范围内具有固有的光学双稳性和温度传感,具有0.2 K的高分辨率。光物理分析表明,在低/高激光功率密度下存在两种光双稳发射。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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