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Abstract: The solid electrolyte Li1.3Zr1.4Ti0.3Al0.3(PO4)3 compound was synthesized by a solid-state reaction. The ceramic samples were sintered 1, 2 and 3h and studied by X-ray and complex impedance spectroscopy in the frequency range from 106 to 1.2×109 Hz in temperature range from 300 to 600K. The investigated compound at room temperature belongs to rhombohedral symmetry (s.g. ) with six formula units in the lattice. Two regions of relaxation dispersion were found. The dispersions are related to the fast Li+ ion transport in the grain and grain boundaries of ceramics. Varying of the sintering time affects the density of the ceramics, the values of total conductivity and its activation energy. The values of grain conductivity, its activation energy, and relaxation frequency in grain, dielectric permittivity and dielectric losses are independent from sintering duration of the ceramics. The value of activation energy of grain conductivity and activation energy of relaxation frequency is the same. That can be attributed to the fact that the temperature dependence of the grain conductivity is caused only by the mobility of Li+ ions, while a number of charge carriers remains constant with temperature. [Copyright &y& Elsevier]

Abstract: Preparation and electrical characterization of NASICON-type compound, Li1.3Ge1.4Ti0.3Al0.3(PO4)3, are described. The solid solution is obtained with Ge4+ →Ti4+ and Ge4+ →Al3+ substitutions in LiGe2(PO4)3. The powder has been fabricated by a solid state reaction and the structural characteristics of it have been studied by X-ray. Ceramic samples have been sintered by varying the sintering duration from 1 to 3h. Samples were studied by complex impedance spectroscopy in the frequency range 1MHz–1.2GHz and temperature range 300–600K. Two regions of relaxation dispersion were found. The dispersions were related to the fast Li+ ion transport in the grains and grain boundaries. Variation of the sintering duration has no considerable effect on electrical properties of the ceramics. [Copyright &y& Elsevier]