Effect of NaF flux on microstructure and thermoluminescence properties of Sm3+ doped CdSiO3 nanophosphor

被引:21
|
作者
Manjunatha, C. [1 ,2 ,3 ]
Nagabhushana, S. M. [1 ,2 ]
Sunitha, D. V. [4 ]
Nagabhushana, H. [4 ]
Sharma, S. C. [4 ]
Venkatesh, G. B. [5 ]
Chakradhar, R. P. S. [6 ]
机构
[1] MS Ramaiah Inst Technol, Dept Chem, Bangalore 560054, Karnataka, India
[2] Visvesvaraya Technol Univ, Belgaum 590018, India
[3] RV Coll Engn, Dept Chem, Bangalore 560059, Karnataka, India
[4] Tumkur Univ, CNR, Tumkur 572103, India
[5] Bangalore Univ, Cent Coll, Dept Chem, Bangalore 560001, Karnataka, India
[6] CSIR Natl Aerosp Labs, Bangalore 560017, Karnataka, India
关键词
Silicates; Luminescence; Halide flux; Combustion synthesis; Phosphor; RARE-EARTH; PHOSPHOR; PHOTOLUMINESCENCE; LUMINESCENCE; NANOPARTICLES; TEMPERATURE; PARTICLES; CERAMICS; ENERGY; SHAPE;
D O I
10.1016/j.jlumin.2012.08.006
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
This work reports the preparation of CdSiO3:Sm3+ (1-7 mol%) nanophosphors by a low temperature solution combustion method. For the first time the effect of NaF flux on the crystallization behavior, morphology, and thermoluminescence property of 5 mol% Sm3+ doped CdSiO3 has been investigated. The nanopowders are well characterized by powder X-ray diffraction (PXRD), Fourier Transform Infra-Red (FT-IR), and scanning electron microscopy (SEM). PXRD results indicate that the powder calcined at 800 degrees C for 2 h has monoclinic phase. SEM results show that the powder is highly porous and the pore size and shape can be modified by the addition of NaF flux. Addition of NaF could lead to formation of particle type morphology and the increase in wt% of NaF changes crystallinity and phase. The thermoluminescence glow curves for 2-6 wt% NaF in CdSiO3:Sm3+ show a single, well resolved glow peak at 126,130 and 150 degrees C, respectively. But for the sample prepared with 8 wt% of NaF flux shows two glow peaks at 148 and 220 degrees C. With the addition of NaF flux, TL intensity can be effectively enhanced. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:432 / 440
页数:9
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