基于结构工程设计的掺杂 Bi3+ 荧光粉实现窄带蓝色发射

IF 3.3 3区 物理与天体物理 Q2 OPTICS
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引用次数: 0

摘要

探索高效窄带发射荧光粉对于高性能背光应用中的白光发光二极管(WLED)至关重要。迄今为止,由于 Bi3+ 通常具有宽带发射特性,因此为新兴应用发现掺杂 Bi3+ 的窄带荧光粉仍具有挑战性。得益于石榴石结构的高度对称晶体环境和紧密连接的刚性结构,我们成功合成了一种新型窄带蓝色荧光粉(Ca4SnGe3O12:Bi3+)。该荧光粉在近紫外(n-UV)区域具有宽激发,并在 442 纳米(FWHM = 36 纳米)处发出窄带蓝光,颜色纯度达 94.7%。本文研究了不同发光中心的分配,以及使用 Zr/Hf 部分替代 Sn 以提高发光性能的方法。本文详细解释了发光行为随之发生变化的原因。使用窄带商用红色 K2SiF6:Mn4+、绿色 β-Sialon:Eu2+和合成蓝色发光材料作为 RGB 发光体,覆盖了美国国家电视系统委员会(NTSC)81% 的色彩空间,显示出液晶显示器(LCD)背光使用的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Realization of narrow-band blue emission based on structurally engineering-designed Bi3+-doped phosphors

The exploration of efficient narrowband emission phosphors is crucial for white light-emitting diodes (WLEDs) in high-performance backlighting applications. Up to now, the discovery of narrow-band Bi3+-doped phosphors for emerging applications remains challenging because Bi3+ typically exhibits broadband emission properties. A novel narrow-band blue phosphor (Ca4SnGe3O12:Bi3+) was successfully synthesized, benefiting from the highly symmetric crystal environment and tightly connected rigid structure of the garnet structure. The phosphor demonstrates broad excitation in the near-ultraviolet (n-UV) region and emits narrowband blue light at 442 nm (FWHM = 36 nm) with a color purity of 94.7 %. In this paper, the assignment of different luminescence centers and the use of Zr/Hf to partially replace Sn to enhance luminescence performance are studied. The reasons for the consequent changes in luminescence behavior are explained in detail. The use of narrowband commercial red K2SiF6:Mn4+, green β-Sialon:Eu2+, and synthetic blue luminescent materials as RGB emitters covered 81 % of the National Television System Committee (NTSC) color space, demonstrating great potential for liquid-crystal-display (LCD) backlight use.

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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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