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机构地区:[1]河南理工大学材料科学与工程学院,焦作454000 [2]盐城工学院江苏省新型环保重点实验室,盐城224051
出 处:《人工晶体学报》2012年第4期1019-1024,共6页Journal of Synthetic Crystals
基 金:河南基础与前沿技术研究计划项目(082300440150);河南省重点科技攻关项目(072102240027);江苏省新型环保重点实验室(AE201150)
摘 要:采用共沉淀法合成了红色荧光粉Sr1-x-yMoO4∶Eu3x+,Gd3y+,分别对样品进行了X射线衍射(XRD)分析、扫面电镜(SEM)和荧光光谱(PL)的测定。结果表明:所合成的样品均为单一纯相四方晶系结构,添加Gd3+(为0.35mol时)使主衍射峰的位置右移了0.35°;SEM照片显示:SrMoO4∶Eu3+和SrMoO4∶Eu3+,Gd3+颗粒尺寸分布相对均匀,为类方块状,颗粒大小约为1~3μm;Gd3+和Eu3+的共掺得到的SrMoO4∶Eu3+,Gd3+在616 nm处主发射峰的发光强度约是SrMoO4∶Eu3+的2.09倍;当掺杂x=0.25 mol和y=0.35 mol时,在近紫外光(395 nm)激发下,SrMoO4∶Eu3+,Gd3+得到616 nm处红光发射极峰。A novel red emitting phosphor Sr1-x-r MoO4 : Eux3+ , Gdy3+ was successfully synthesized by co- precipitation method. The crystal structure, morphology and luminescent properties of samples were characterized by X-ray diffraction( XRD), scanning electron microscope( SEM), and photoluminescence spectrophotometer (PL). The results indicated that all the phosphor are isostructural and share a tetragonal scheelite structure of space group I41/a88 ; After adding Gd3+ (y -0.35 mol), it is found the main diffraction peak position shifted to the right of 0. 35% The results of SEM show that the particles size of SrMoO4: Eu3+ and SrMoO4: Eu3+ , Gd3+ is relatively uniform, displays the blocks structure of regular shape, which size is about 1-3μm; Under 395 nm, it is found that the luminescent intensity of SrMoO4: Eu3+, Gd3+ is about 2.09 times higher than that of SrMoO4: Eu3+ phosphor; the main emission spectrum peak at 616 nm achieves the maximum in Eu3+ and Gd3+ co-doped SrMoO4 phosphor when x =0.25 mol and y = 0.35 mol.
关 键 词:白光LED SrMoO4∶Eu3+ Gd3+ 红色荧光粉 共沉淀法
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