Design and control of the luminescence in Cr3+-doped NIR phosphors via crystal field engineering

被引:88
作者
Gao, Tongyu [1 ,2 ,3 ]
Zhuang, Weidong [1 ,2 ,3 ]
Liu, Ronghui [1 ,2 ,3 ]
Liu, Yuanhong [1 ,2 ,3 ]
Chen, Xiaoxia [1 ,2 ,3 ]
Xue, Yuan [1 ,2 ,3 ]
机构
[1] GRINM Grp Co Ltd, Natl Engn Res Ctr Rare Earth Mat, Beijing 100088, Peoples R China
[2] GRIREM Adv Mat Co Ltd, Beijing 100088, Peoples R China
[3] Gen Res Inst Nonferrous Met, Beijing 100088, Peoples R China
基金
国家重点研发计划;
关键词
Near-infrared (NIR) phosphor; Luminescence tuning; Crystal field engineering; GARNET PHOSPHORS; LIGHT-SOURCES; PHOTOLUMINESCENCE; SPECTROSCOPY; CR3+;
D O I
10.1016/j.jallcom.2020.156557
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Near-infrared (NIR) light-emitting diodes (LEDs) have currently attracted increasing attention owing to high efficiency and longevity. Accordingly, NIR phosphor, as the indispensable role in NIR LEDs, needs to be enriched to meet widespread applications worldwide. Benefitting from structural tunability of LaSc3B4O12(LSB), a sequence of broadband phosphors, with continuous-tunable luminescence toward longer wavelength, can be designed by regulating the crystal field environment of the Cr3+ via substituting the Sc3+ by Y(3+ )in LSB host. The correlations among structural evolution, crystal field environment, and luminescence properties of LaSc3-xYxB4O12(LSYB): Cr3+ (0 <= x <= 1.3) have been discussed in detail. Furthermore, substitution Y3+ for Sc3+ in LSB causes band gap variation of host lattice, demonstrated by the diffuse reflectance spectra, consequently resulting in improved quantum yield (QY), and mitigated thermal quenching behavior of LSYB: Cr(3+ )compared to that of Y3+-free sample. The above results demonstrate the superiority of crystal field engineering in exploring broadband NIR phosphors with modified luminescence performance for potential application in NIR pc-LEDs. (C) 2020 Elsevier B.V. All rights reserved.
引用
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页数:9
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