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作 者:王晓丽[1] 杨智[1] 何锋[1] 李永明[1] 高振华[2] 黄艳[2] 陶冶[2]
机构地区:[1]云南师范大学化学化工学院,云南昆明650500 [2]中国科学院高能物理研究所北京同步辐射装置,北京100049
出 处:《发光学报》2014年第2期172-177,共6页Chinese Journal of Luminescence
基 金:云南省自然科学基金(2007B201M)资助项目
摘 要:提出一种合成LaAlO3的新方法,该方法操作简单、成本低、无污染。将化学计量比的反应物La(OH)3/La2O3和Al(OH)3放入反应釜中,于220℃温度下水热活化处理,快速加热至900℃反应即可得到LaAlO3。XRD结果表明,所合成的LaAlO3为三方晶系。PL结果表明,所合成的LaAlO3∶Eu3+的主要发射为Eu3+的5D0→7F1磁偶极跃迁发射和5D0→7F2电偶极跃迁发射,红橙比随着Eu3+离子掺杂量的增加而变大。在VUV-UV激发光谱中,LaAlO3∶Eu3+位于VUV光谱区的基质吸收很弱,而位于~315 nm的O2--Eu3+的电荷迁移跃迁带(CT)则较强。A facile,environmentally friendly,low cost method was employed to synthesize perovskite-type LaAlO 3 powders.The stoichiometric mixtures of La( OH) 3 / La 2 O 3,and Al( OH) 3 were activated by a hydrothermal treatment in teflon-lined stainless steel autoclave at 220 ℃ for 3 d,and then the precursors were quickly heated to 900 ℃ and reacted for 5 h to obtain LaAlO 3.The obtained samples were characterized by X-ray diffraction( XRD) and photoluminescence( PL) spectra.XRD result shows that LaAlO 3 crystal structure belongs to the rhombohedral system with the space group of R 3c( No.167).PL results indicate the main emissions of LaAlO 3 ∶ Eu3 +come from the magnetic dipole-dipole5D 0 →7F 1 transition and the electric dipole-dipole5D 0 →7F 2 transition.The ratio value of the intensity of Eu3 +:5D 0 →7F 2 transition to the intensity of Eu3 +:5D 0 →7F 1 transition increases with the increase of Eu3 +concentration.Host absorption of LaAlO 3 ∶ Eu3 +in the VUV range is weaker than that of O2--Eu3 +charge transfer band in the UV range.
关 键 词:LaAlO3∶Eu3+ 绿色化学合成 X射线粉末衍射 发光性质
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