Thermal behaviour and photoluminescence properties of Er- and Nd-doped yttrium aluminate glasses
Autor: | Milan Parchovianský, Nurshen Mutlu, Jana Valúchová, Alfonz Plško, Róbert Klement, Anna Prnová, Dušan Galusek |
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Rok vydání: | 2020 |
Předmět: |
Materials science
Photoluminescence Annealing (metallurgy) Aluminate Doping Analytical chemistry chemistry.chemical_element 02 engineering and technology Yttrium 021001 nanoscience & nanotechnology Condensed Matter Physics 01 natural sciences 010406 physical chemistry 0104 chemical sciences law.invention Amorphous solid chemistry.chemical_compound chemistry law Emission spectrum Physical and Theoretical Chemistry Crystallization 0210 nano-technology |
Zdroj: | Journal of Thermal Analysis and Calorimetry. 142:129-138 |
ISSN: | 1588-2926 1388-6150 |
DOI: | 10.1007/s10973-020-09816-3 |
Popis: | Yttrium aluminate glasses (76.8 mol% of Al2O3, 23.2 mol% of Y2O3) doped with Er3+ and Nd3+ ions at different concentration levels (0.25 mol%, 0.5 mol% and 0.75 mol% Er2O3/Nd2O3) were prepared by flame synthesis in the form of glass microspheres. The prepared samples were XRD amorphous, without presence of any crystalline phases in measured patterns. The two exothermic effects (~ 940, ~ 1010 °C), which can be assigned to the two steps of YAG crystallization, were observed in the DSC records of all prepared samples. The high temperature XRD measurements showed YAG (900–1200 °C) and α-Al2O3 (1300–1450 °C) phase crystallization. The emission spectra were measured in the VIS and NIR regions for Er-doped samples and in the NIR region for Nd-doped samples. All measured emission spectra contain of characteristic bands due to the typical 4f–4f transitions within the Er3+ and Nd3+ ions. Comparison of the measured intensities of Er-doped samples made it evident that the highest intensities were obtained for the 0.5 mol% Er2O3-doped sample (in both the NIR and VIS spectral regions). The maximum intensity for Nd-doped samples was found when the sample was doped with 0.75 mol% of Nd2O3. The slowly increasing of emission intensities in samples after 20 min annealing at 1000 °C and Stark splitting of emission bands in samples after 40 and 60 min annealing at 1000 °C and after 20, 40 and 60 min annealing at 1500 °C was observed. |
Databáze: | OpenAIRE |
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