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作 者:张新民[1] 梁宏斌[2] 余瑞金[2] 田梓峰[2] 苏锵[2]
机构地区:[1]中南林业科技大学材料科学与工程学院,湖南长沙410004 [2]中山大学光电材料与技术国家重点实验室∥化学与化学工程学院,广东广州510275
出 处:《中山大学学报(自然科学版)》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)
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 ).
关 键 词:发光 UV—Vis 荧光粉 SrGdGa3O7:Eu^3+
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