Judd-Ofelt and quantum cutting analysis of Eu3+ or Pr3+ doped β-NaGdF4 nanorods obtained by rapid coprecipitation method

被引:14
作者
Cheroura, Y. [1 ,2 ]
Smara, Z. [1 ,3 ]
Potdevin, A. [1 ]
Boyer, D. [1 ]
Chafa, A. [3 ]
Ziane, O. [2 ]
Mahiou, R. [1 ]
机构
[1] Univ Clermont Auvergne, CNRS, SIGMA Clermont, Inst Chim Clermont Ferrand, F-63000 Clermont Ferrand, France
[2] USTHB, Fac Phys, Lab Elect Quant, El Alia Bab Ezzouar 16111, Alger, Algeria
[3] USTHB, Fac Phys, Lab Sci Nucl & Interact Rayonnement Mat, El Alia Bab Ezzouar 16111, Alger, Algeria
关键词
Nanorods; Fluorides; Luminescence; Judd-Ofelt theory; ONE-POT SYNTHESIS; RARE-EARTH IONS; ENERGY-TRANSFER; LUMINESCENCE; NANOPARTICLES; EXCITATION; NANOPHOSPHORS; ULTRASMALL; SIZE;
D O I
10.1016/j.materresbull.2020.110809
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Pure hexagonal beta-NaGdF4 and Eu3+ or Pr3+-doped beta-NaGdF4 nanocrystals in shape of nanorods of similar to 140 nm of length have been synthesized using a simple and rapid coprecipitation method. XRD analysis evidenced pure single phases exhibiting characteristic luminescence of Eu3+ or Pr3+ ions when excited under UV or blue radiations. Samples gave rise to intense orange-red emission and quite white emission in the case of respectively Eu(3+)or Pr(3+)doped samples. Optical properties are discussed in the frame of Judd-Ofelt theory and considering that an energy transfer occurs between active ions. Notably it was found that the quantum-cutting by a two-step energy transfer from Gd3+ to Eu3+ can improve the red emission of Eu3+ ions under near-VUV excitation. Such quantum-cutting mechanism has been also considered in the case of Pr3+ doped beta-NaGdF4. However, the efficiency of both processes in comparison with literature suggest that only one part of the energy in the excited states within Gd3+ can be transferred to Eu3+ for its red emission. In the case of Pr3+ ions, the energy is more probably released through the self-trapped exciton emission certainly due to the lack of resonant VUV excitation.
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页数:11
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