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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12128/20012
Title: Dipole relaxation process and giant dielectric permittivity in Eu3+- doped CdMoO4 single crystal
Authors: Sawicki, Bogdan
Tomaszewicz, E.
Groń, Tadeusz
Berkowski, M.
Głowacki, M.
Oboz, Monika
Kusz, Joachim
Pawlus, Sebastian
Keywords: Scheelite; Single crystal; Solid solution; Paramagnetic behaviour; Relaxation process; Giant dielectric permittivity
Issue Date: 2020
Citation: Journal of Materiomics, (2020)
Abstract: Single crystal of Eu3+-doped cadmium molybdate (Cd0.9268 M 0.0244Eu0.0488MoO4, where M denotes cationic vacancies) has been successfully grown by the Czochralski method in air and under 1 MPa. X-ray diffraction analysis indicates that as-grown single crystal exhibits tetragonal scheelite-type structure (a = b = 5.16188(14) A; c = 11.2080(5) A; space group I41/a). Eu3+ ions do not show long-range order and they are randomly distributed in CdMoO4 framework substituting Cd2+ ones. UVevis diffuse reflectance measurements revealed very close optical band gap (Eg) values, i.e. ~1.74 eV along [100] and [001] crystallographic directions that are twice smaller than Eg of microcrystalline pure CdMoO4 as well as powder Eu3+-doped single crystal. Magnetic and electrical studies of Eu3+-doped cadmium molybdate single crystal showed a paramagnetic and n-type semiconducting behaviour with the metal-insulator transition above 350 K along both crystallographic directions. Dielectric results analysis using the Cole-Cole fit function revealed that the dipole relaxation process has different time scale depending on the crystallographic direction and exhibits Arrhenius temperature dependence for both studied directions. This fact is accompanied by the colossal dielectric permittivity with er > 8 • 103. The above results are considered in the framework of narrow europium multiplets of energy comparable to thermal energy.
URI: http://hdl.handle.net/20.500.12128/20012
DOI: 10.1016/j.jmat.2020.12.010
ISSN: 2352-8478
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