4.7 Article

Linear dielectric thermodynamics: A new universal law for optical, dielectric constants

Journal

JOURNAL OF THE AMERICAN CERAMIC SOCIETY
Volume 104, Issue 5, Pages 2087-2101

Publisher

WILEY
DOI: 10.1111/jace.17594

Keywords

dielectric constant; dielectric materials; electric permittivity; entropy; optical materials; refractive index; thermodynamics

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The thermodynamics of linear dielectric are formally developed to explore the isothermal and adiabatic temperature-pressure dependence of dielectric constants. The argument for the dielectric constant's isentropic temperature dependence is thermodynamic and applicable to all physical models. The isentropic slope of the displacement field vs the electric field shows instability at high temperatures due to changes in the curvature of the temperature dependence of the dielectric constant, impacting the electronic entropy contribution.
The thermodynamics of linear dielectric are formally developed to explore the isothermal and adiabatic temperature-pressure dependence of dielectric constants. The refractive index of optical materials is widely measured in the literature: it is both temperature and pressure dependent. The argument to establish the dielectric constant's isentropic temperature dependence is a thermodynamic one and is thus applicable to all physical models that describe electron clouds and electronic resonances within materials. The isentropic slope of the displacement field vs the electric field at all temperatures is described by an adiabatic dielectric constant in an energy-per-unit mass system. This slope is shown through the electronic part of the entropy to be unstable at high temperatures due to the change in the curvature of the temperature dependence of the dielectric constant. The electronic entropy contribution for optical, thermo-electro materials has negative heat capacities which are unacceptable. The dielectric constant's temperature and pressure dependence is predicted to be only dependent on the specific volume so isentropes are always positive. A new universal form for the dielectric constant follows from this hypothesis: the dielectric constant is proportional to the square root of the specific volume for fully dense solids.

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