Optical path coupling regulation of excitation light and LuAG: Ce phosphor ceramics for high-luminous-efficiency laser lighting

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Yiwei Zhu , Yang Li , Tingting Wang , Zhihao Li , Jian Kang , Le Zhang , Jun Zou
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Abstract

In the preparation processes of laser lighting sources, although optimizing phosphor materials remains the primary strategy to enhance phosphor conversion efficiency, the excitation modes applied to these materials have emerged as an equally effective means. In this study, the luminescence performance of a remote LD-based light source was effectively regulated by controlling the exciting distance and exciting angle between phosphor ceramics and blue LD. Under optimized conditions with an exciting distance of 200 mm and an angle of 60°, a maximum LF of 27,124 lm was achieved, corresponding to a calculated LER of 219.6 lm W−1. Oblique incidence excitation of phosphor ceramics was found to exhibit significantly enhanced luminescence performance relative to conventional vertical incidence. The operating temperature of the ceramics decreased gradually with increasing exciting angles, primarily due to decreased power density caused by spot size expansion. These findings reveal that tailoring excitation geometry can effectively balance thermal management and optical efficiency in phosphor ceramics-based remote LD systems, offering critical insights for the design of high-power transmission-type packaging devices.
高光效激光照明中激发光与LuAG: Ce荧光陶瓷的光路耦合调节
在激光光源的制备过程中,虽然优化荧光粉材料仍然是提高荧光粉转换效率的主要策略,但应用于这些材料的激发模式已经成为同样有效的手段。在本研究中,通过控制荧光粉陶瓷与蓝色LD之间的激励距离和激励角度,有效地调节了远程LD光源的发光性能。在激励距离为200 mm、角度为60°的优化条件下,最大LF达到27124 lm,对应的计算LER为219.6 lm W−1。研究发现,相对于传统的垂直入射激发,荧光陶瓷的斜入射激发具有显著增强的发光性能。随着激发角的增加,陶瓷的工作温度逐渐降低,这主要是由于光斑尺寸的膨胀导致功率密度的降低。这些发现表明,在基于荧光粉陶瓷的远程LD系统中,定制激发几何结构可以有效地平衡热管理和光效率,为高功率传输型封装器件的设计提供重要见解。
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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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