Issue 15, 2012

Morphology and phase control of fluorides nanocrystals activated by lanthanides with two-model luminescence properties

Abstract

The morphology, size and phase control of luminescent fluoride nanocrystals through doping has become a new research hotspot due to their improved properties. In this work, Yb3+ ions, as one of the most efficient sensitizers for various lanthanide activators, were doped in NaGd(Y)F4 nanocrystals. The results show that no obvious influence was observed for Yb3+-doped NaYF4 nanocrystals, while the influence of Yb3+ doping on NaGdF4 nanocrystals was remarkable. The NaGd1−xYbxF4 nanocrystals were synthesized by a hydrothermal route and had a morphology of rice-like nanorods. By controlling the synthesis parameters, the average size and slenderness of the nanocrystals increased gradually with addition of Yb3+ ions. In contrast, the NaGd1−xYbxF4 nanocrystals maintained a hexagonal phase, which is more beneficial for application as a luminescent host, until the content of Yb3+ ions reached x = 0.9. The growth and transformation mechanism of NaGd1−xYbxF4 nanocrystals was proposed to be a result of the competition between ion diffusion and an Oswald ripening process. Photoluminescence (PL) spectra confirm the efficient up-conversion and near-infrared (NIR) two-model luminescence properties of Er3+ (Tm3+) activated NaGd(Y)1−xYbxF4 nanocrystals. Simulated analysis results indicate that a colloidal solution of mixed luminescent nanocrystals is expected to find application as the activated medium of three dimensional displays and a broadband optical amplifier.

Graphical abstract: Morphology and phase control of fluorides nanocrystals activated by lanthanides with two-model luminescence properties

Supplementary files

Article information

Article type
Paper
Submitted
25 Apr 2012
Accepted
25 May 2012
First published
28 May 2012

Nanoscale, 2012,4, 4658-4666

Morphology and phase control of fluorides nanocrystals activated by lanthanides with two-model luminescence properties

G. Dong, B. Chen, X. Xiao, G. Chai, Q. Liang, M. Peng and J. Qiu, Nanoscale, 2012, 4, 4658 DOI: 10.1039/C2NR30998J

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