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The Li4xTi1-xP2O7(x = 0, 0.06, 0.1, 0.2) powders have been synthesized by the solid state reaction and their ceramics have been sintered. The Li4xTi1-xP2O7(x = 0.06, 0.1, 0.2) compounds have cubic superstructure 3×3×3 (space group Pa-3), which is also typical for TiP2O7pyrophosphate. The electrical properties of the ceramics were investigated in the frequency range of 10 to 3·109Hz and temperature interval of 400–720 K by impedance spectroscopy. The relaxation dispersion region in the conductivity and dielectric permittivitty spectra of Li4xTi1-xP2O7(x = 0, 0.06, 0.1, 0.2) ceramics was found. [ABSTRACT FROM AUTHOR]

LiFeP2O7and Li0.9Fe0.9Ti0.1P2O7were synthesised by solid-state reaction and ceramics were sintered. The structure of compounds was studied in the temperature range 300–700 K by X-ray diffraction. Ceramics’ surfaces were investigated by scanning electron microscope. Binding energies of Fe 2p, P 2p and O 1s core levels at ceramics’ surfaces have been determined by X-ray photoelectron spectroscopy and different valence states of Fe and P were detected. Elemental compositions of the compounds were studied by energy dispersive X-ray spectrometer. Impedance spectroscopy was performed in the frequency range 10 Hz–3 GHz and in the temperature interval 400–700 K. The changes of the activation energy of ionic conductivity at 528 and 550 K for LiFeP2O7and Li0.9Fe0.9Ti0.1P2O7, respectively, were found. The phenomena can be related to disordering in the unit cells of the compounds. [ABSTRACT FROM AUTHOR]

Copyright of Lithuanian Journal of Physics is the property of Lithuanian Academy of Sciences and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Lithuanian Journal of Physics is the property of Lithuanian Academy of Sciences and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

At room temperature solid electrolyte Li3−xSc2−xZrx(PO4)3 (x = 0, 0.1) compounds belong to monoclinic symmetry (space group P21/n) and the compound with x = 0.2 belongs to orthorhombic symmetry (Pbcn). At 900 K all the investigated compounds belong to orthorhombic symmetry (space group Pbcn). Anomalies of enthalpy, change of activation energy of ionic conductivity, anomalies of dielectric permittivity in the temperature range 420 K–660 K of investigated compounds with x = 0 and 0.1 were found. The phenomena are related to structure phase transition in the compounds. The relaxation dispersion regions were found in conductivity spectra for the all investigated samples. The frequency dispersion regions are caused by the relaxation processes in grain, grain – boundaries and electrodes. The temperature dependencies of the bulk conductivity and relaxation frequency in the bulk are governed by the same activation energy. It is shown that major role in the temperature dependence of bulk conductivity is played by Li+ ion mobility, which increases as temperature increases. [ABSTRACT FROM PUBLISHER]

The solid electrolyte Li2.9Sc1.9-yYyZr0.1(PO4)3 (where y = 0, 0.1) compounds belong to monoclinic symmetry (space group P21/n) at room temperature. The Zr 3d, Sc 2p, P 2p, Y 3d, O 1s, and Li 1s core level X-ray photoelectron spectra (XPS) were fitted. The Li ions in ceramics without Y occupy two different positions and in the ceramics with Y they occupy one position in the lattice. The deconvolutions of the Zr 3d, P 2p, Sc 2p, and Y 3d core level XPS are associated with different valence states on the surfaces of the investigated ceramics. Anomalies of enthalpy, change of activation energy of ionic conductivity, anomalies of dielectric permittivity in the temperature range 420-520 K of investigated compounds were found. The phenomena are related to diffuse structure phase transition in the compounds. At temperatures 600 and 900 K, the compounds belong to orthorhombic symmetry (space group Pbcn). [ABSTRACT FROM AUTHOR]

Abstract: Li1.3AlyYx−yTi1.7(PO4)3 (x=0.3; y=0.1, 0.2) solid electrolyte compounds were synthesized by solid state reaction and studied by X-ray diffraction. At room temperature the compounds belong to a rhombohedral symmetry (space group Rc) with six formula units in the unit cell. Ti 2p, O 1s, P 2p, Li 1s, Y 3d, and Al 2p core level XP spectra at Li1.3AlyYx−yTi1.7(PO4)3 (x=0.3; y=0.1, 0.2) ceramic surfaces have been determined by XPS. The measurements of the electrical properties of the ceramic samples in the frequency range 10Hz–1MHz were carried out by a two probe method and a four probe method. The measurements in the microwave range (3·105–3·109 )Hz were performed in a coaxial line, the part of the inner conductor which was replaced by the sample. The investigation of the electrical properties of the ceramic samples was carried out in air in the temperature range (300 to 700)K. The increase of the stoichiometric factor y of the compounds leads to the increase in the total and bulk conductivities of ceramics and decreases their activation energies. [Copyright &y& Elsevier]

Abstract: The powder of Li1+xAlyScx−yTi2−x(PO4)3 with x=0.3 and y=0.1, 0.15, 0.2 has been prepared by solid state reaction and the ceramics have been sintered. The results of X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS) and impedance spectroscopy up to 109 Hz are presented. At room temperature the compounds belong to the rhombohedral symmetry (space group R3̅c). Ti 2p, P 2p, O 1s, Sc 2p, Al 2p, and Li 1s core level XP spectra''s were fitted. The values of binding energies of core level XP spectra''s, splitting energies of Ti 2p3/2–Ti 2p1/2, Sc 2p3/2–Sc 2p1/2, P2p3/2–P2p1/2 spin-orbit doublets, and amount of the elements with different binding energies were found to be dependent on stoichiometric factor y. The elemental compositions are defined by EDX. Impedance spectroscopy study in the frequency range 10Hz–3GHz have shown three relaxation dispersion regions of electrical properties and the processes are thermally activated. The high frequency dispersion region may be attributed to the relaxation processes in bulk, while lower dispersion regions are related to the processes in grain boundaries and blocking Pt electrodes. [Copyright &y& Elsevier]

Abstract: The solid electrolyte Li2.8Sc1.8−y Y y Zr0.2(PO4)3 (where y =0, 0.1) compounds were synthesized by a solid state reaction and studied by X-ray diffraction. At room temperature the compounds belong to orthorhombic symmetry (space group Pbcn) with four formula units in the unit cell. Elemental compositions and binding energies of Zr 3d, Sc 2p, Y 3d, P 2p, O 1s, and Li 1s core level at Li2.8Sc1.8Zr0.2(PO4)3 and Li2.8Sc1.7Y0.1Zr0.2(PO4)3 ceramics’ surfaces have been determined by XPS. Impedance spectroscopy of the ceramics has been performed in the frequency range 10–3×109 Hz in the temperature interval 300–600K. The substitution of Sc by Zr and Y in the host compound Li3Sc2(PO4)3 leads to the increase of ionic conductivity of the new ceramics. [Copyright &y& Elsevier]

Abstract: It was shown in many literature sources that ionic conductivity of the LiTi2(PO4)3 compound was increased by several orders substituting Ti4+ ion by trivalent ions. In the case of substituting by La3+ there was no success to synthesize single phase material. The two phases were obtained and conductivity increased considerably. In the present work the substitution Ti4+ →La3++ Li+ in the LiTi2(PO4)3 system was studied by XRD, SEM, XPS, WDX, and impedance spectroscopy. The powder was prepared by solid state reaction with relative mixture of initial materials to obtain Li1+ x La x Ti2− x (PO4)3 with x =0.3, but the impurity of LaPO4 was detected by XRD. The ceramic samples were sintered with different sintering duration to check the influence of sintering on composition and electrical properties. [Copyright &y& Elsevier]