Parametrization of linear dielectric response

W. A. B. Evans, D. M. Heyes, J. G. Powles, and G. Rickayzen
Phys. Rev. E 83, 046601 – Published 1 April 2011

Abstract

The quantum linear response of a dielectric to an external electric field yields expressions for the dielectric susceptibility and the associated impulse response function. These are measured properties that, during analysis, are often “curve-fitted” to diverse forms of parametric functional forms that shall herein be referred to as fit-functions. The main purpose of this paper is to show, from a very general linear response formalism that encompasses virtually all microscopic models of dielectric response, that there are constraints on the forms that the susceptibilities must obey and to examine common parametrizations of the dielectric function in light of these constraints. Naturally these constraints should, whenever possible, be in-built into the fit-functions employed. The linear response approach due to Madden and Kivelson [Adv. Chem. Phys. 56, 467 (1984)], where the cause is considered to be a uniform external field, Eext(t), is utilized as it affords a much more straightforward interaction term, viz., M·Eext(t), (M being the system’s total electric dipole moment operator) than would be the case if the mean internal field (or “Maxwell field”) were taken as the cause. It is shown that this implies definite relations between the quasipermittivity, ζ(ω), of the Madden-Kivelson approach and the normal permittivity, χ(ω)ε(ω)ε0. These relations indicate a condition for the divergence of the normal susceptibility, which, arguably, marks the onset of a ferroelectric transition in “sufficiently polar” dielectrics. Finally, some common parametric “fit-function” forms are investigated as to whether they comply with the constraints that the formalism imposes, and examples are given of their associated Cole-Cole plots in typical cases involving one or more relaxation times.

    • Received 23 September 2010

    DOI:https://doi.org/10.1103/PhysRevE.83.046601

    ©2011 American Physical Society

    Authors & Affiliations

    W. A. B. Evans*

    • School of Physical Sciences, University of Kent, Canterbury CT2 7NH, United Kingdom

    D. M. Heyes

    • Department of Mechanical Engineering, Imperial College London, Exhibition Road, South Kensington, London SW7 2AZ, United Kingdom

    J. G. Powles

    • School of Engineering, Swansea University, Singleton Park, Swansea SA2 8PP, United Kingdom

    G. Rickayzen§

    • Division of Chemistry, Faculty of Health and Molecular Sciences, University of Surrey, Guildford GU2 7XH, United Kingdom

    • *Author to whom all correspondence should be addressed: w.a.b.evans@kent.ac.uk
    • d.heyes@imperial.ac.uk
    • j.powles@swansea.ac.uk
    • §g.rickayzen@surrey.ac.uk

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    Issue

    Vol. 83, Iss. 4 — April 2011

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