Sm3+ doped K3Gd3B4O12: An orange-emitting phosphor for white light-emitting diodes

被引:18
作者
Zhao, Ji [1 ]
Huang, Shan-Xiu [1 ]
Zhao, Dan [1 ,2 ]
Huang, Cun-Han [4 ]
Ma, Ming-Jie [1 ,3 ]
Zhang, Rui-Juan [4 ]
Fan, Yun-Chang [1 ]
Liu, Bao-Zhong [1 ,3 ]
Gao, Jia-Wang [1 ]
Zong, Qiu [1 ]
Yu, Ya-Ping [1 ]
机构
[1] Henan Polytech Univ, Coll Chem & Chem Engn, Jiaozuo 454000, Henan, Peoples R China
[2] State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
[3] Henan Polytech Univ, Henan Key Lab Coal Green Convers, Jiaozuo 454000, Henan, Peoples R China
[4] Henan Polytech Univ, Acad Affairs Off, Jiaozuo 454000, Henan, Peoples R China
来源
OPTIK | 2018年 / 159卷
基金
中国国家自然科学基金;
关键词
Luminescence; Sm3+ activator; Borate; Phosphor; Energy transfer; PHOTOLUMINESCENCE PROPERTIES; LUMINESCENT PROPERTIES; EU3+;
D O I
10.1016/j.ijleo.2018.01.043
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
K3Gd3-xSmxB4O12 orange phosphors were synthesized via the high temperature solid-state reaction method. The phase composition, morphology, particle size and luminescent properties were investigated using X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence spectra (PL), respectively. The SEM images showed that the doped sample exhibited an irregular morphology with e diameter of about 2 mu m. The optimum doping concentration was found to be 15 mol% for Sm3+ ion and the critical distance R-c was calculated to be 7.8846 angstrom. Under near-UV light (405 nm) excitation, they showed intense orange emission centered at 603 nm because of the (4)G(5/2) -> H- 6(7/2) transition of Sm(3+ )activator. Under 276 nm excitation, there existed a charge transfer from Gd3+ to Sm3+ and the charge transfer efficiency of K3Gd3-xSmxB4O12 can reach 99.88%. The CIE coordinates of phosphor K3Gd2.8Sm0.15B4O12 are calculated to be (0.5895, 0.4096) and the color purity was estimated to be around 88%, which indicates that the phosphor may be potentially excited NUV chips for application in W-LEDs. (C) 2018 Elsevier GmbH. All rights reserved.
引用
收藏
页码:115 / 122
页数:8
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