Non-linear dielectric signatures of entropy changes in liquids subject to time dependent electric fields

• Published in: The Journal of chemical physics Vol. 144; no. 11; pp. 114501 - 114505
• Main Author: Richert, Ranko
• Format: Journal Article
• Language: English
• Published: United States American Institute of Physics 21.03.2016
• Subjects: ACTIVATION ENERGY; Amplitudes; DIELECTRIC MATERIALS; Dielectric polarization; ELECTRIC FIELDS; ENTROPY; EXPERIMENTAL DATA; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; Mathematical models; NONLINEAR PROBLEMS; NUMERICAL SOLUTION; PARTICLE TRACKS; TEMPERATURE DEPENDENCE; Thermodynamic properties; TIME DEPENDENCE
• ISSN: 0021-9606; 1089-7690; 1089-7690
• DOI: 10.1063/1.4943885

A model of non-linear dielectric polarization is studied in which the field induced entropy change is the source of polarization dependent retardation time constants. Numerical solutions for the susceptibilities of the system are obtained for parameters that represent the dynamic and thermodynamic behavior of glycerol. The calculations for high amplitude sinusoidal fields show a significant enhancement of the steady state loss for frequencies below that of the low field loss peak. Also at relatively low frequencies, the third harmonic susceptibility spectrum shows a “hump,” i.e., a maximum, with an amplitude that increases with decreasing temperature. Both of these non-linear effects are consistent with experimental evidence. While such features have been used to conclude on a temperature dependent number of dynamically correlated particles, N corr, the present result demonstrates that the third harmonic susceptibility display a peak with an amplitude that tracks the variation of the activation energy in a model that does not involve dynamical correlations or spatial scales.