Development of a novel Eu3+-doped tantalate red-emitting phosphor for w-LEDs application

被引:0
|
作者
Zeng, Fan [1 ,2 ]
Ru, Jingjing [1 ]
Zhao, Bing [3 ]
Guo, Feiyun [4 ]
Chen, Jianzhong [4 ]
机构
[1] Ningde Normal Univ, Fujian Prov Univ, Coll Chem & Mat, Key Lab Green Energy & Environm Catalysis, Ningde 352100, Peoples R China
[2] Fujian Normal Univ, Sch Environm & Resources, Sch Carbon Neutral & Modern Ind, Fuzhou 350007, Peoples R China
[3] Ningde Normal Univ, Coll Informat & Mech & Elect Engn, Ningde 352100, Peoples R China
[4] Fuzhou Univ, Coll Chem, Fuzhou 350108, Peoples R China
关键词
Phosphor; Tantalate; LED device; Rare earths; HIGH COLOR PURITY; LUMINESCENCE PROPERTIES; THERMAL-STABILITY; HIGHLY EFFICIENT; LIGHT; PHOTOLUMINESCENCE; BA; SR;
D O I
10.1016/j.jre.2023.07.0141002-0721
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two novel phosphors LiBa4(1-x)Eu4xTa3O12 (H-LBTO:xEu(3+)) and Li0.25Ba1-xEuxTa0.75O3 (C-LBTO:xEu(3+)) were prepared successfully by a molten salt method. The transformation between these two structures was realized by changing the sintering temperature or changing the Eu3+ ions concentration, which was also demonstrated by the X-ray diffraction (XRD), scanning electron microscopy (SEM), diffuse reflectance spectra (DRS), and photoluminescence excitation (PLE) analyses. Both the sintering temperature and the Eu3+ ions doping concentration have significant impact on the formation of the crystal phase. All these phosphors sintered at 1023 K exhibit two major luminescence lines at 594 and 614 nm under near-UV light of 395 nm excitation, corresponding to Eu3+ ions typical transitions of D-5(0)-> F-7(1) and D-5(0)-> F-7(2). The optimum concentration of Eu3+ ions is 9 mol% for C-LBTO:xEu(3+) samples and the quenching interaction type is the nearest-neighbor ion interaction. The thermal stability of the C-LBTO:0.09Eu(3+) sample was investigated in detail and the device application further suggests that C-LBTO:0.09Eu(3+) can be used as a red phosphor for near-UV excited w-LEDs in lighting. (c) 2023 Chinese Society of Rare Earths. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:1479 / 1488
页数:10
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