Crystal Structure Stabilization of Gadolinium Aluminum Garnet (Gd3Al5O12) and Photoluminescence Properties

被引:16
作者
Li, Jinkai [1 ]
Li, Ji-Guang [1 ]
Wu, Xiaoli [1 ]
Liu, Shaohong [1 ]
Li, Xiaodong [1 ]
Sun, Xudong [1 ]
机构
[1] Northeastern Univ, Minist Educ, Key Lab Anisotropy & Texture Mat, Adn Sch Mat & Met, Shenyang 110004, Liaoning, Peoples R China
来源
TESTING AND EVALUATION OF INORGANIC MATERIALS III | 2013年 / 544卷
关键词
gadolinium aluminate garnet; lattice stabilization; photoluminescence; LUMINESCENCE; PHASE; PARTICLES; Y3AL5O12; PHOSPHOR; RAY; IR;
D O I
10.4028/www.scientific.net/KEM.544.245
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
To suppress the thermal decomposition and to stabilize the crystal structure of Gd3Al5O12 (GdAG) garnet, doping GdAG with smaller Ln(3+) (Ln=Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y, respectively) to form (Gd,Ln)AG solid solutions was proposed in work. Carbonate precursors of (Gd,Ln)AG with an approximate composition of (NH4)(x)(Gd,Ln)(3)Al-5(OH)(y)(CO3)(z)center dot nH(2)O were synthesized via coprecipitation from a mixed solution of ammonium aluminum sulfate and rare earth nitrate, using ammonium hydrogen carbonate as the precipitant. The precursors and the calcination derived oxides were characterized using FT-IR spectroscopy, DTA/TG, XRD, BET and FE-SEM. The results showed that smaller Ln(3+) doping can indeed stabilize GdAG against its thermal decomposition to a mixture of GdAlO3 (GdAP) and Al2O3 phases at elevated temperatures and at the same time effectively lowers the temperature for garnet crystallization. The carbonate precursors are loosely agglomerated and the resultant (Gd,Ln)AG powders show good dispersion and a fairly uniform particle morphology. The (Gd,Ln)AG solid solutions exhibit decreasing lattice parameters along with decreasing radius of the dopant ions at the same dopant content of 50 at%. Photoluminescence properties of some of the garnet solid solutions are also studied. The materials developed herein may potentially be used for photoluminescent and scintillation applications.
引用
收藏
页码:245 / 251
页数:7
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