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Synthesis, structure, EPR studies and up-conversion luminescence of ZnO:Er-Yb@GdO nanostructures
ZnO:Er 3+ -Yb 3+ @Gd 2 O 3 nanostructures were obtained by " wet " chemistry methods - the sol-gel technique for the preparation of ZnO and ZnO:Er 3+ -Yb 3+ nanoparticles (NPs), and the seed deposition method for obtaining Gd 2 O 3 . The crystal structure, morphology, phase and elemental c...
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Published in: | RSC advances 2016-09, Vol.6 (92), p.8935-89312 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | |
Online Access: | Get full text |
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Summary: | ZnO:Er
3+
-Yb
3+
@Gd
2
O
3
nanostructures were obtained by "
wet
" chemistry methods - the sol-gel technique for the preparation of ZnO and ZnO:Er
3+
-Yb
3+
nanoparticles (NPs), and the seed deposition method for obtaining Gd
2
O
3
. The crystal structure, morphology, phase and elemental composition, resonant microwave absorption of rare earth ions, point defects in the ZnO:Er
3+
-Yb
3+
@Gd
2
O
3
crystal structure and up-conversion luminescence were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) with energy dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR) spectroscopy, and optical spectroscopy. The crystallization temperature (600 °C) of the Gd
2
O
3
phase on the ZnO surface was found. As-obtained ZnO:Er
3+
-Yb
3+
NPs (with size ∼7 nm) are highly crystalline and monodispersed. ZnO:Er
3+
-Yb
3+
NPs annealing at 900 °C leads to the formation of highly polydispersed ZnO:Er
3+
-Yb
3+
NPs, covered by a Gd
2
O
3
shell. The process of the incorporation of the rare earth ions into the ZnO structure, as well as the effect of Gd
2
O
3
content on the morphology and visible up-conversion (UC) luminescence in ZnO:Er
3+
-Yb
3+
matrices were studied.
ZnO:Er
3+
-Yb
3+
@Gd
2
O
3
nanostructures were obtained by "
wet
" chemistry methods - the sol-gel technique for the preparation of ZnO and ZnO:Er
3+
-Yb
3+
nanoparticles (NPs), and the seed deposition method for obtaining Gd
2
O
3
. |
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ISSN: | 2046-2069 |
DOI: | 10.1039/c6ra18393j |