Morphological investigations on the solid electrolyte Li3.6Ge0.6V0.4O4 and use in a solid state lithium battery |
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Authors: | L Hoffart D M Schleich |
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Institution: | (1) ISITEM - Laboratoire de Génie des Matérieaux, Université de Nantes, Rue Christian Pauc, La Chantrérie, CP - 30 23, F-44087 Nantes Cedex 03, France |
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Abstract: | The development of a solid state thin film lithium battery system needs a detailed investigation of the electrolyte as well
as the electrodes. The realisation of a total solid state battery includes the assumption, that the interfacial contact between
the electrodes and the electrolyte is as good as possible. The interfacial resistance should be low for an easily intercalation
or deintercalation of lithium at the electrodes and the ionic conductivity of the electrolyte should be high.
A further critical aspect of the solid state battery is the porosity of the electrodes and the electrolyte. A homogeneous
surface coverage and a high density are useful for a high contact concentration between the grains of electrolyte itself and
between the electrolyte and the electrodes. As a possible electrolyte we have investigated the system Li4GeO4/Li3VO4, which we prepared in the stoichiometry Li3.6 Ge0.6 V0.4 O4. This lithium conducting system shows a high lithium conductivity of about 4 x 10−5 S/cm at room temperature and higher values at elevated temperatures. The conductivity is the result of interstitial Li cations
in the solid state solution.
The deposition of the inorganic thin film was done by a spray pyrolysis technique on different substrates. A variety of different
substrates were investigated as a function of adhesion and modified surface conditions. The aim is to find a correlation between
the substrate and the morphology of the thin film. The temperature of the deposition was varied between 400 and 600 °C. The
temperature dependent cristallinity was also studied. Furthermore the change of the unit cell volume and its constants a,
b and c has been investigated as a function of temperature by high temperature diffractometry. The thermal expansion coefficient
of the electrolyte could be calculated, to examine stresses with various substrates.
Paper presented at the 2nd Euroconference on Solid State Ionics, Funchal, Madeira, Portugal, Sept. 10–16, 1995 |
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