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  • 1
    Digitale Medien
    Digitale Medien
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 11 (1981), S. 211-231 
    ISSN: 0084-6600
    Quelle: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Thema: Maschinenbau
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Solid State Ionics 18-19 (1986), S. 454-460 
    ISSN: 0167-2738
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Ionics 4 (1998), S. 200-206 
    ISSN: 1862-0760
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract The conductivity of glasses in the P2O5−[(1−x) V2O5−x Na2O] system is studied as a function of temperature and composition. For all compositions, the conductivity variations as a function of temperature follow an Arrhenius type relationship: $$\sigma = \frac{A}{T}\exp \left( { - \frac{{E_a }}{{RT}}} \right)$$ . The activation energies and pre-exponential factors corresponding to the V2O5 richest compositions are lower than that corresponding to the ionic ones. Isothermal variations of the conductivity as a function of composition show a deep minimum for a molar ratio x near 0.65. On either side of this minimum, the conductivity is mainly electronic (x〈0.7) or ionic (x〉0.8). The variations are interpreted assuming a prevailing diluting effect of the non predominantly present oxide without any interactions between the electronic and ionic charge carriers.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 1862-0760
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Accurate conductivity measurements as a function of hydrostatic pressure (1 – 5000 bars) and temperature (20 – 150 °C) have been performed on a cationic inorganic glass and a cationic conducting polymer. In both cases, the conductivity decreases with increasing pressure and the variation of Inσ at constant temperature as a function of pressure gives straight lines with slopes which allow an “activation volume”, ΔV*, to be obtained by the relationship (∂lnσ/∂P)T=− (ΔV*/RT). In the case of silver metaphosphate glass, studied below its glass transition temperature, the activation volume (5 cm3⋅mol−1) is temperature independent and equal to the molar volume of the silver cation. Since the transport mechanism implies a free energy barrier, this volume is a real activation volume, corresponding to the difference in volume between a mole of the moving species in its activated transition state and its volume at normal equilibrium. In the case of the sodium conductive polymer, studied above its glass transition temperature, the previous thermodynamic definition does not hold any more because the ionic transport follows a V.T.F. behaviour rather than an Arrhenius law. Consequently, ΔV* is an “apparent activation volume” without a simple physical meaning. Experimental values are higher (20 to 30 cm3⋅mol−1) and decrease with temperature. In this polymer, the mobility of the charge carriers is interpreted in terms of free volume mechanism. From the variations of the apparent activation volume with temperature, the critical free volume Vf* for an elementary displacement is estimated. For the Na+ conductive ionomer Vf* is estimated to be equal to 13 cm3⋅mol−1. This large value would indicate the participation of macromolecular chain segments in the ionic transport.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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