TY  - JOUR
AU  - Đorđević, Vesna R.
AU  - Brik, Mikhail G.
AU  - Srivastava, Alok M.
AU  - Medić, Mina M.
AU  - Vulić, Predrag J.
AU  - Glais, Estelle
AU  - Viana, Bruno
AU  - Dramićanin, Miroslav
PY  - 2017
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7197
AB  - Herein, the synthesis, structural and crystal field analysis and optical spectroscopy of Mn4+ doped metal titanates ATiO(3) (A = Ca, Mg) are presented. Materials of desired phase were prepared by molten salt assisted sol-gel method in the powder form. Crystallographic data of samples were obtained by refinement of X-ray diffraction measurements. From experimental excitation and emission spectra and structural data, crystal field parameters and energy levels of Mn4+ in CaTiO3 and MgTiO3 were calculated by the exchange charge model of crystal-field theory. It is found that crystalline field strength is lower (Dq = 1831 cm(-1)) in the rhombohedral Ilmenite MgTiO3 structure due to the relatively longer average Mn4+-O2- bond distance (2.059 angstrom), and higher (Dq = 2017 cm(-1)) in orthorhombic CaTiO3 which possess shorter average Mn4+-O2- bond distance (1.956 angstrom). Spectral positions of the Mn(4+2)Eg - GT (4)A(2g) transition maxima is 709 nm in MgTiO3 and 717 nm in CaTiO3 respectively in good agreement with calculated values. (C) 2017 Elsevier B.V. All rights reserved.
T2  - Optical Materials
T1  - Luminescence of Mn4+ ions in CaTiO3 and MgTiO3 perovskites: Relationship of experimental spectroscopic data and crystal field calculations
VL  - 74
SP  - 46
EP  - 51
DO  - 10.1016/j.optmat.2017.03.021
ER  - 

@article{
author = "Đorđević, Vesna R. and Brik, Mikhail G. and Srivastava, Alok M. and Medić, Mina M. and Vulić, Predrag J. and Glais, Estelle and Viana, Bruno and Dramićanin, Miroslav",
year = "2017",
abstract = "Herein, the synthesis, structural and crystal field analysis and optical spectroscopy of Mn4+ doped metal titanates ATiO(3) (A = Ca, Mg) are presented. Materials of desired phase were prepared by molten salt assisted sol-gel method in the powder form. Crystallographic data of samples were obtained by refinement of X-ray diffraction measurements. From experimental excitation and emission spectra and structural data, crystal field parameters and energy levels of Mn4+ in CaTiO3 and MgTiO3 were calculated by the exchange charge model of crystal-field theory. It is found that crystalline field strength is lower (Dq = 1831 cm(-1)) in the rhombohedral Ilmenite MgTiO3 structure due to the relatively longer average Mn4+-O2- bond distance (2.059 angstrom), and higher (Dq = 2017 cm(-1)) in orthorhombic CaTiO3 which possess shorter average Mn4+-O2- bond distance (1.956 angstrom). Spectral positions of the Mn(4+2)Eg - GT (4)A(2g) transition maxima is 709 nm in MgTiO3 and 717 nm in CaTiO3 respectively in good agreement with calculated values. (C) 2017 Elsevier B.V. All rights reserved.",
journal = "Optical Materials",
title = "Luminescence of Mn4+ ions in CaTiO3 and MgTiO3 perovskites: Relationship of experimental spectroscopic data and crystal field calculations",
volume = "74",
pages = "46-51",
doi = "10.1016/j.optmat.2017.03.021"
}

Đorđević, V. R., Brik, M. G., Srivastava, A. M., Medić, M. M., Vulić, P. J., Glais, E., Viana, B.,& Dramićanin, M.. (2017). Luminescence of Mn4+ ions in CaTiO3 and MgTiO3 perovskites: Relationship of experimental spectroscopic data and crystal field calculations. in Optical Materials, 74, 46-51.
https://doi.org/10.1016/j.optmat.2017.03.021

Đorđević VR, Brik MG, Srivastava AM, Medić MM, Vulić PJ, Glais E, Viana B, Dramićanin M. Luminescence of Mn4+ ions in CaTiO3 and MgTiO3 perovskites: Relationship of experimental spectroscopic data and crystal field calculations. in Optical Materials. 2017;74:46-51.
doi:10.1016/j.optmat.2017.03.021 .

Đorđević, Vesna R., Brik, Mikhail G., Srivastava, Alok M., Medić, Mina M., Vulić, Predrag J., Glais, Estelle, Viana, Bruno, Dramićanin, Miroslav, "Luminescence of Mn4+ ions in CaTiO3 and MgTiO3 perovskites: Relationship of experimental spectroscopic data and crystal field calculations" in Optical Materials, 74 (2017):46-51,
https://doi.org/10.1016/j.optmat.2017.03.021 . .