Abstract
The polycrystalline zinc gallate ZnGa2O4: Mn2+ and ZnGa2O4: Mn2+, Eu3+ samples have been synthesized via high-temperature solid-state reaction ceramic technique. The obtained ceramics have been characterized employing the methods of X-ray diffraction analysis, transmission electron microscopy, energy-dispersive X-ray spectroscopy, positron annihilation lifetime spectroscopy and optical-luminescent spectroscopy. The XRD analysis testified in favor of successful formation of spinel structure in the prepared samples with small amount of additional phase observed in the ZnGa2O4: Mn2+, Eu3+ ceramics. The grains of irregular shape with a homogeneous distribution of Eu3+ ions in a volume were identified with TEM technique. The band gap of ZnGa2O4: Mn2+ spinel was estimated from optical absorption spectra in UV–Vis range. The characteristic bands related to electronic transitions of Mn2+ and Eu3+ ions were found in optical absorption and excitation spectra. The photoluminescence emission spectra exhibited matrix luminescence along with emission band of Mn2+ ions and narrow lines of Eu3+ ions in blue, green and red spectral region, respectively. The intensity ratio of Eu3+ emission lines confirms the high asymmetry around Eu3+ ions. These findings correlate well with results of positron annihilation lifetime spectroscopy showing intense reduction of positron trapping rate deeply in ceramics grains due to Eu3+ ions penetration.
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Acknowledgements
Kravets O. is thankful to the Head of Physical Organic Chemistry Group, Prof. Dr. Christoph Lambert, Julius Maximilian’s University of Würzburg, Germany for provided time for working in the laboratory and obtained absorption spectra. This work was partially supported by the Ministry of Education and Science of Ukraine under the program for support of young scientists (project no. 0116U008069).
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Kravets, O., Zaremba, O., Shpotyuk, Y. et al. Structure, morphology and optical-luminescence investigations of spinel ZnGa2O4 ceramics co-doped with Mn2+ and Eu3+ ions. Appl Nanosci 9, 907–915 (2019). https://doi.org/10.1007/s13204-018-0681-4
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DOI: https://doi.org/10.1007/s13204-018-0681-4