一种用于固态照明的热稳定磷酸钇锂荧光粉

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Zhiqin Yang , Youkui Zheng , Jie Ma , Jingkai Jiao , Xiaonan Wang , Yue Li , Yingfan Niu , Bo Wang , Jing Zhu
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引用次数: 0

摘要

在本工作中,将三价镝与磷酸钇锂LiY5P2O13(LYP)掺入,获得黄色发射材料。通过XRD研究、DFT计算和实验发光光谱的综合分析,确定了引入的Dy3+活化剂的结晶位置。在353nm激发下,LYP:Dy3+荧光粉由于主要的4F9/2而显示出亮黄色发射→6H13/2跃迁(577nm)。当Dy3+含量超过0.07mol时,发光猝灭发生,这源于偶极-偶极相互作用。此外,标题磷光体优异的热稳定性行为(在423K下为84%)和良好的抗色移性(在473K下为0.00634)通过温度依赖性研究得到了证明。最终,用LYP:0.07Dy3+和商业材料制备的w-LED表现出稳定的白光发射输出(0.3595.0.3179),具有高Ra(85)和低CCT(4203K)。所有的研究都表明LYP:Dy3+材料在固态插图领域是一个有前景的候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A thermally stable lithium yttrium phosphate phosphor for solid-state lighting

A thermally stable lithium yttrium phosphate phosphor for solid-state lighting

In this work, trivalent dysprosium was incorporated with lithium yttrium phosphate LiY5P2O13 (LYP), obtaining a yellow-emitting material. The crystallographic sites of introduced Dy3+ activators are determined through the comprehensive analysis of the XRD investigation, DFT computation, and experimental luminescence spectra. Under 353 nm excitation, the LYP:Dy3+ phosphor shows bright yellow emission owing to dominant 4F9/2 → 6H13/2 transition (577 nm) of Dy3+. The luminescence quenching occurs when the Dy3+ content exceeds 0.07 mol, originating from the dipole–dipole interaction. Furthermore, the excellent thermal stability behavior (84 % at 423 K) and good resistance to color shifting (0.00634 at 473 K) for title phosphor are manifested by temperature-dependent investigation. Eventually, the w-LED fabricated with LYP:0.07Dy3+ and commercial materials exhibits stable white-emitting output (0.3595, 0.3179) with high Ra (85) and low CCT (4203 K). All the study demonstrates that the LYP:Dy3+ material is a perspective candidate in solid-state illustration field.

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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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