White light emission from Er2O3 nano-powder excited by infrared radiation

被引:19
作者
Tabanli, Sevcan [1 ,2 ]
Eryurek, Gonul [1 ,2 ]
Di Bartolo, Baldassare [2 ]
机构
[1] Istanbul Tech Univ, Dept Phys Engn, TR-34469 Istanbul, Turkey
[2] Boston Coll, Dept Phys, Chestnut Hill, MA 02467 USA
关键词
Thermal decomposition method; White light production; Upconversion; Erbium oxide; Nanocrystal; UP-CONVERSION LUMINESCENCE; EXCITATION; COLOR; POWER; YB3+;
D O I
10.1016/j.optmat.2017.04.007
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Phosphors of Er2O3 nano-crystalline powders were synthesized by the thermal decomposition method. The structural properties of the nano-powders were investigated with XRD and HRTEM measurements. The cubic phase with a = 10.540 angstrom was the only phase observed. The average crystalline sizes and the widths of the grain size distribution curves were determined to be 27.2, 18.7 and 9.7 nm, respectively. The spectroscopic properties of the Er2O3 nano-powder were studied by measuring the luminescence, decay and rise patterns under 808 and 975 nm diode laser excitations. A peculiar effect of the pressure was observed since an optically active ion (Er) is part of the complex and not a dopant. A broad band of the white light emission combined with blue, green and red up-conversion emission bands of Er3+ ions were observed at 0.03 mbar pressure under both excitation wavelengths. Only, an intense broad band white light emission was observed from these nanocrystals at atmospheric pressure. Rising patterns show that the white light intensity reaches its maximum value more rapidly under 975 nm excitation although it decays slower than that of 808 nm excitation. The color quality parameters such as the color coordinate (CRI), correlated color temperature and the color rendering index were found to vary with both the excitation wavelength and the ambient pressure indicating that these nanocrystals could be considered good white light emitting source under the infrared excitations. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:207 / 213
页数:7
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