Energy Transfer Mechanism of KAlSiO4 : Re3+ (Re = Dy/Sm) Phosphors

被引:1
|
作者
Yantake, Reziwanguli [1 ,2 ]
Sun Lanlan [1 ,2 ]
Wang Qingling [1 ,2 ]
Sidike, Aierken [1 ,2 ]
机构
[1] Xinjiang Normal Univ, Sch Phys & Elect Engn, Lab Mineral Luminescent Mat & Microstruct Xinjian, Urumqi 830054, Xinjiang, Peoples R China
[2] Xinjiang Normal Univ, Sch Phys & Elect Engn, Lab Novel Light Source & Micro Nanoopt, Urumqi 830054, Xinjiang, Peoples R China
关键词
materials; KAlSiO4 : Dy3+; Sm3+ phosphors; high temperature solid phase method; energy transfer; internal quantum efficiency; SM3+; DY3+;
D O I
10.3788/LOP57.211601
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
A series of Dy3+, Sm3+ co-doped KAlSiO4 phosphor materials were prepared by the high temperature solid phase method. The experimental results show that the doping of a small amount of Dy3+ and Sm3+ does not change the crystal structure of KAlSiO4. When KAlSiO4 1% Dy3+, woo Sm3+ is excited at the characteristic excitation wavelength of Dy3+, there occurs a resonant non-radiative energy transfer from Dy3+ to Sm3+ in samples. Meanwhile, the color coordinate shift is very small and there exists a red shift at 528 nm and a blue shift at 713 nm. In contrast, when KAlSiO4 1.50 Sm3+, Dy3+ is excited at the characteristic excitation wavelength of Sm3+ the emission spectrum is very similar to that of KAlSiO4 1. 5% Sm3+ and there are no characteristic emission peaks of Dy3+. However, the luminous intensity of Sm3+ at 651 nm is increased by 6.5 times, which indicates that there does not exist energy return from Sm3+ to Dy3+ and the doping of Dy3+ promotes crystal lattice matching and greatly enhances the luminous intensity of Sm3+. Theoretical calculations show that the maximum energy transfer efficiency from Dy3+ to Sm3+ reaches up to 52% and the energy transfer interaction is electric quadrupole-quadrupole interaction. The color coordinates of phosphors are all around (0.41, 0. 51) and located in the yellow-green area. The internal quantum yield under 386 nm excitation gradually increases from 25. 8 0% to 42. 6 %.
引用
收藏
页数:9
相关论文
共 18 条
  • [1] Luminescent Properties of Ca2GdZr2Al3 : Mn4+ and Bi3+ Codoped Phosphors
    Chen Kai
    Wang Xiaojun
    Yang Guohui
    Liang Lifang
    Meng Lili
    Zhang Lixia
    [J]. ACTA OPTICA SINICA, 2019, 39 (02)
  • [2] Halimulati Dilare, 2019, SHANDONG IND TECHNOL, V7, P243
  • [3] Yellow Persistent Phosphor Ba13.35Al30.7Si5.3O70:Eu2+,Tm3+ from the Energy Regulation of Rare-Earth Ions
    Jiang, Haijing
    Jia, Yonglei
    Qu, Tianliang
    Pan, Yao
    Yang, Kaiyong
    Luo, Hui
    [J]. ACS OMEGA, 2019, 4 (04): : 6923 - 6930
  • [4] Luminescence Properties and Energy Transfer Mechanism of Sr3P4O13:Ce3+, Tb3+ Green Phosphors
    Mi Wanxin
    Cao Lili
    Chu Siqi
    Ma Hongping
    [J]. ACTA OPTICA SINICA, 2019, 39 (08)
  • [5] Analysis of energy transfer based emission spectra of (Sm3+, Dy3+): Li2O-LiF-B2O3-CdO glasses
    Naresh, V.
    Buddhudu, S.
    [J]. JOURNAL OF LUMINESCENCE, 2014, 147 : 63 - 71
  • [6] Tunable emissions from Dy3+/Sm3+ ions co-activated SrY2O4:Er3+ nanocrystalline phosphors for LED and FED applications
    Pavitra, E.
    Raju, G. Seeta Rama
    Yu, Jae Su
    [J]. JOURNAL OF ALLOYS AND COMPOUNDS, 2014, 592 : 157 - 163
  • [7] Synthesis and luminescent properties of Ca2Li2BiV3O12: Eu3+ phosphor
    [J]. Qiu, K.-H. (qkh2188@163.com), 1600, Chines Academy of Sciences (33):
  • [8] Luminescent Properties and Energy Transfer of K2MgSiO4 : Eu3+, Tb3+ Phosphors
    Shen Yu-ling
    Wan Ying
    Ye Ying
    Wang Qing-ling
    Sidike, Aierken
    [J]. ACTA PHOTONICA SINICA, 2019, 48 (02)
  • [9] [石文杰 Shi Wenjie], 2014, [中国稀土学报, Journal of the Chinese Society of Rare Earths], V32, P164
  • [10] Heavy Mn2+ Doped MgAl2O4 Phosphor for High-Efficient Near-Infrared Light-Emitting Diode and the Night-Vision Application
    Song, Enhai
    Jiang, Xingxing
    Zhou, Yayun
    Lin, Zheshuai
    Ye, Shi
    Xia, Zhiguo
    Zhang, Qinyuan
    [J]. ADVANCED OPTICAL MATERIALS, 2019, 7 (24)