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一种新型发红光材料SrGdGa3O7:Eu^3+及其性质研究 被引量:2

A New Phosphor SrGdGa_3O_7:Eu^(3+) and its Luminescent Properties
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摘要 采用高温固相法合成了发红光的荧光粉SrGdGa3O7:Eu3+。漫反射光谱和激发光谱中Eu3+的电荷迁移带、Eu3+离子f→f跃迁以及Gd3+离子8S7/2→6I7/2的跃迁相互吻合;监测Eu3+离子的特征发射,激发谱中有Gd3+离子的激发线表明存在Gd3+→Eu3+的能量传递。发射光谱中以5D0→7F2跃迁为主,表明Eu3+离子所占据的晶体学格位没有对称中心的Cs格位。根据低温下的发射光谱计算了7F1和7F2能级完全解除简并后的每个分裂能级的位置。Eu3+的发射发生明显的温度猝灭现象,同时发射谱线的分辨率也逐渐降低。Eu3+离子的5D0→7F2跃迁在不同温度下的荧光衰减曲线相似;随着温度的升高,荧光发射强度衰减越快,但是仍然处于毫秒数量级;5D0→7F2跃迁是宇称和自旋禁阻的跃迁,所以荧光衰减时间比较长。 Phosphor SrGdGa3O7:Eu^3+ has been synthesized by solid-state reaction at high temperature. The bands of f→f transfer of Eu^3+ and ^*S7/2→^6I7/2 transfer of Gd^3+ appear in the exicitation spectrum, which is consistent with diffuse reflectance spectrum. When monitored by 613 nm, there are ^8S7/2 -6I7/2 and ^8S7/2 -^6P7/2 transitions of Gd^3+, indicating that the energy transfer from Gd^3+ to Eu^3+ happens. Emission spectrum is dominated by the main lines at 613 nm due to the ^5D0 -^7F2 transition, indicating Eu^3+ occupies Gd site (Cs) without inversion symmetry. The splitted energy levels of ^7F1 and ^7F2 have been calculated by emission spectrum at 12 K. Emissionintensity of Eu^3+ decreases gradually with temperature increasing, and the resolution of emission peak also decreases. Decay curves of Eu^3+ (^5Do→^7 F2 ) at different temperature are similar and emission intensity decrease with temperature increasing. The lifetime of Eu^3+ is in the order of millisecond, which is reasonable for the forbidden transfer (^5Do→^7F2 ).
出处 《中山大学学报(自然科学版)》 CAS CSCD 北大核心 2008年第2期62-64,共3页 Acta Scientiarum Naturalium Universitatis Sunyatseni
基金 国家自然科学基金资助项目(20171046)
关键词 发光 UV—Vis 荧光粉 SrGdGa3O7:Eu^3+ luminescence UV - Vis phosphors SrGdGa3O7:Eu^3+
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  • 1KODAMA N, SASAKI N, YAMAGA M, et al. Long-lasting phosphorescence of Eu^2+ in melilite [J]. J Lumin, 2001,94 -95 : 19.
  • 2YAMAGA M, TANII Y, et al. Mechanism of long-lasting phosphorescence process of Ce^3+ -doped Ca2Al2SiO7 melilite crystals [J]. Physical Review B,2002,65:235108 -235118.
  • 3WANG X J, JIA D, YEN W M. Mn^2+ activated green, yellow,and red long persistent phosphors [ J]. J Lumin, 2003,102 - 103:34 - 37.
  • 4KACZKAN M, PRACKA I, MALINOWSKI M. Optical transitions of Ho^3+ in SrLaGa3O7 [ J]. Optical Materials, 2004,25 : 345.
  • 5SHIONOYA S, YEN W M. Phosphor Handbook [M]. CRC Press, 1999 : 193.

同被引文献15

  • 1叶瑞伦 吴伯麟 曾科 等.高温型Ca2SiO4·CaCl2的晶体结构.硅酸盐学报,1984,:504-507.
  • 2WANMAKER W L, VERRIET J G. Luminescence of phosphors with tricalcium monosilicate dichloride as the host lattice[ J]. Philips Research Reports, 1973, 28 (1) : 80 - 83.
  • 3LIU J, LIAN H Z, SUN J Y, et al. Characterization and properties of green emitting Ca3Si04Cl2: Eu^2+ power phosphor for white light-emitting diodes [ J ]. Chem Lett, 2005, 34(10) : 1340 - 1341.
  • 4LIU J, LIAN H Z, SHI C S, et al. Eu^2+ - doped high- temperature phase Ca3SiO4Cl2 a yellowish orange phos-phor for white light-emitting diodes [ J ]. J Electrochem Soc, 2005, 152( 11 ) :G880 - G884.
  • 5NEERAJ S, KIJIMA N, CHEETHAM A K. Novel red phosphors for solid-state lighting: the system NaM ( WO4 )2-x (MoO4 )x: Eu^3+ ( M = Gd, Y, Bi) [ J ]. Chem Phys Lett, 2004, 387:2 -6.
  • 6WANG Z L, LIANG H B, ZHOU L Y, et al. Lumines- cence of ( Li0.333 Na0.334 K0.333 ) Eu ( MoO4 )2 and its application in near UV InGaN-based llght-emitting diode [ J ]. Chem Phys Lett, 2005, 412:313 -316.
  • 7WANG Z L, LIANG H B, WANG J, et al. Red-light-e- mitting diodes fabricated by near- ultraviolet InGaN chips with molybdate phosphors[ J]. Appl Phys Lett, 2006, 89 (7) : 071921/1 -071921/3.
  • 8SOHN K S, PARK D H, CHO S H, et al. Computational evolutionary optimization of red phosphor for use in tricolor white LEDs[J]. Chem Mater, 2006, 18(7):1768 - 1772.
  • 9CHILS, LIU RS, LEE BJ. Synthesis of Y2O3:Eu, Bi red phosphors by homogeneous coprecipitation and their photoluminescence behaviors [ J ]. J Electrochem Soc, 2005,152 : J93 - J98.
  • 10CZAYA R. Preparation and crystallographic data of calcium silicate calcium chloride [ J ]. Zeitschrift fuer Anorganische und Allgemeine Chemie, 1970, 375 (2) : 124 - 127.

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