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Eu掺杂2ZnO·2.2B2O3·3H2O红色荧光粉发光性能的研究
Luminescent Properties of Eu-Doped 2ZnO·2.2B2O3·3H2O
【作者】 乐天; 曾庆光; 张梅; 黄天; 颜强望; 王忆;
【Author】 LE Tian~1 ZENG Qing-guang~(2,*) ZHANG Mei~2 HUANG Tian~2 YAN Qiang-wang~2 WANG Yi~2 (1 School of Chemical and Environmental Engineering,Wuyi University, Guangdong,Jiangmen,529020) (2 School of Applied Physics and Materials,Wuyi University,Guangdong,Jiangmen,529020)
【机构】 五邑大学化学与环境工程学院; 五邑大学应用物理与材料学院;
【摘要】 采用水热法合成2ZnO·2.2B2O3·3H2O:Eu3+红色荧光粉。其形貌、结构和光学性能分别用扫描电镜、X-射线衍射和荧光光谱仪进行表征。扫描电镜图片显示样品的尺寸分布在0.1~1μm范围内。X-射线衍射结果表明:所合成的粉末样品的基质材料为2ZnO·2.2B2O3·3H2O;随着Eu掺杂浓度的升高,样品向无定形状态转变。研究样品的激发和发射光谱发现:当激发波长为253 nm(属于Eu3+—O2-电荷迁移带吸收)时,样品中Eu3+的发光强度要远远强于394nm激发;当Eu3+的掺杂浓度增大到24%(摩尔比:Eu:Zn=24%)时,出现浓度猝灭效应。随着样品退火温度的升高,由X射线衍射谱可知:样品逐渐变成为无定形的玻璃态。当样品的退火温度升高至400℃时,Eu3+的发光强度降低,且同时出现了一个新的宽发射峰(发射中心位于470 nm,对应于Eu2+的发射峰),这说明了在此温度下部分Eu3+被还原成Eu2+。
【Abstract】 A new kind red phosphor,Eu3+doped 2ZnO·2.2B2O3·3H2O,has been synthesized by hydrothermal method.The morphology,crystal phase and luminescent properties of zinc borate were investigated by scanning electronic microscopy(SEM),X-ray diffraction(XRD)and fluorescence spectrometer,respectively.The SEM image shows the particle size of the as-prepared powder is between 0.1 to 1μm.The X-ray diffraction show the matrix of samples is 2ZnO·2.2B2O3·3H2O;the crystalline state of the as-prepared powder is transferred to glass state with the increasing of Eu content.The excitation and emission spectra of Eu-doped 2ZnO·2.2B2O3-3H2O reveals that the emission intensity of Eu excited by 253 nm(the charge transfer band of Eu3+)is much stronger than it excited by 394 nm.The optimism doping concentration is 24%(molar ratio Eu:Zn=24%).Meanwhile,glass state induced by increasing the annealing temperature is observed.When the annealing temperature is up to 400℃,decrease in the emission intensity of Eu3+and appearance of a new fluorescence peak assigned to the transition of Eu2+(its emission centre at 470 nm)is observed.
- 【会议录名称】 第七届全国稀土发光材料学术研讨会会议论文摘要集
- 【会议名称】第七届全国稀土发光材料学术研讨会
- 【会议时间】2011-05-12
- 【会议地点】中国浙江杭州
- 【分类号】TN104.3;O614.33
- 【主办单位】中国稀土学会发光专业委员会、中国物理学会发光分科学会