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作 者:霍涌前[1] 陈小利[1] 张谋真[1] 石蕾[1] 刘啟瑞
机构地区:[1]延安大学化学与化工学院,陕西延安716000
出 处:《化学与生物工程》2014年第12期9-11,共3页Chemistry & Bioengineering
基 金:国家自然科学基金资助项目(21101133)
摘 要:分别采用化学沉淀法、微波法、水热法制备了SrMoO4:0.05Eu3+,0.05Gd3+荧光粉,并通过X-射线粉末衍射(XRD)、荧光光谱和扫描电子显微镜(SEM)对其晶体结构、荧光光谱和形貌进行了表征。结果表明:SrMoO4:0.05Eu3+,0.05Gd3+的结构属体心四方晶系;其宽激发带由Eu3+-O2-、Gd3+-O2-电荷迁移带和Mo6+-O2-基质吸收峰组成,荧光发光以在616nm处Eu3+的5 D0→7 F2跃迁引起的红光发光最强;254nm紫外光激发时,化学沉淀法制备SrMoO4:0.05Eu3+,0.05Gd3+的发光峰比SrMoO4:0.05Eu3+的相应发光峰强度增大,这是由于Gd3+向Eu3+的能量传递敏化增强了Eu3+的发光。SrMoO4:0.05Eu3+,0.05Gd3+phosphors were prepared by chemical precipitation method,microwave method and hydrothermal method.The crystal structure,luminescence property and morphology of the samples were characterized by XRD,fluorescence spectroscopy,SEM.XRD Analysis confirmed the samples exhibited a body-centered tetragonal crystal structure.Fluorescence spectroscopy showed that the broad excitation bands belonged to charge transfer band of Eu3+-O2-,Gd3+-O2-and the host absorption of Mo6+-O2-in SrMoO4:0.05Eu3+,0.05Gd3+,and the most intense peak was located at 616 nm,which corresponded to the 5D0→7F2transitions of Eu3+.The photoluminescence intensity of Eu3+in SrMoO4:0.05Eu3+,0.05Gd3+prepared by chemical precipitation method increased due to an efficient energy migration process of Gd3+→Eu3+occurred in the phosphors under 254 nm light excitation.
关 键 词:SrMoO4:0.05Eu3+ 0.05Gd3+ 光致发光 荧光粉
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