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Tuning Green to Red Color in Erbium Niobate Micro- and Nanoparticles
Tetragonal Er(0.5)Nb(0.5)O(2) and monoclinic ErNbO(4) micro- and nanoparticles were prepared by the citrate sol–gel method and heat-treated at temperatures between 700 and 1600 °C. ErNbO(4) revealed a spherical-shaped crystallite, whose size increased with heat treatment temperatures. To assess thei...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998491/ https://www.ncbi.nlm.nih.gov/pubmed/33800356 http://dx.doi.org/10.3390/nano11030660 |
Sumario: | Tetragonal Er(0.5)Nb(0.5)O(2) and monoclinic ErNbO(4) micro- and nanoparticles were prepared by the citrate sol–gel method and heat-treated at temperatures between 700 and 1600 °C. ErNbO(4) revealed a spherical-shaped crystallite, whose size increased with heat treatment temperatures. To assess their optical properties at room temperature (RT), a thorough spectroscopic study was conducted. RT photoluminescence (PL) spectroscopy revealed that Er(3+) optical activation was achieved in all samples. The photoluminescence spectra show the green/yellow (2)H(11/2), (4)S(3/2)→(4)I(15/2) and red (4)F(9/2)→(4)I(15/2) intraionic transitions as the main visible recombination, with the number of the crystal field splitting Er(3+) multiplets reflecting the ion site symmetry in the crystalline phases. PL excitation allows the identification of Er(3+) high-energy excited multiplets as the preferential population paths of the emitting levels. Independently of the crystalline structure, the intensity ratio between the green/yellow and red intraionic transitions was found to be strongly sensitive to the excitation energy. After pumping the samples with a resonant excitation into the (4)G(11/2) excited multiplet, a green/yellow transition stronger than the red one was observed, whereas the reverse occurred for higher excitation photon energies. Thus, a controllable selective excited tunable green to red color was achieved, which endows new opportunities for photonic and optoelectronic applications. |
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