Effect of Li+ co-doping on structural and luminescence properties of Mn4+ activated magnesium titanate films

The effect of Li + co-doping on crystal phase formation and photoluminescence (PL) of Mn 4+ activated magnesium titanate films produced by a solid state reaction method at different temperatures (800–1200 °C) has been investigated by using X-ray diffraction (XRD), diffuse reflectance and PL spectros...

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Bibliographic Details
Published inJournal of materials science. Materials in electronics Vol. 29; no. 18; pp. 15613 - 15620
Main Authors Borkovska, L., Khomenkova, L., Markevich, I., Osipyonok, M., Stara, T., Gudymenko, O., Kladko, V., Baran, M., Lavoryk, S., Portier, X., Kryshtab, T.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.09.2018
Springer Nature B.V
Springer Verlag
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Summary:The effect of Li + co-doping on crystal phase formation and photoluminescence (PL) of Mn 4+ activated magnesium titanate films produced by a solid state reaction method at different temperatures (800–1200 °C) has been investigated by using X-ray diffraction (XRD), diffuse reflectance and PL spectroscopy. The chemical composition of sintered films was estimated by energy dispersive X-ray spectroscopy. The concentration of Mn impurity estimated by Electron spin resonance was about 5 × 10 16 cm −3 . The XRD study of the annealed films revealed several magnesium titanate crystal phases, such as Mg 2 TiO 4 , MgTiO 3 and MgTi 2 O 5 . The contribution of each phase depended strongly on the annealing temperature and the presence of Li + additive. Furthermore, Li + co-doping facilitated the formation of both MgTiO 3 and Mg 2 TiO 4 phases, especially at lower annealing temperatures. The PL spectra showed two bands centered at 660 and 710 nm and ascribed to the 2 E →  4 A 2 spin-forbidden transition of the Mn 4+ ion in the Mg 2 TiO 4 and MgTiO 3 , respectively. In Li co-doped films, the integrated intensity of Mn 4+ luminescence was found several times stronger compared to Li-undoped films that was ascribed mainly to flux effect of lithium.
ISSN:0957-4522
1573-482X
DOI:10.1007/s10854-018-9153-6