Maxwell–Wagner–Sillars polarization
In dielectric spectroscopy, large frequency dependent contributions to the dielectric response, especially at low frequencies, may come from build-ups of charge. This, so-called Maxwell-Wagner-Sillars polarization (or often just Maxwell-Wagner polarization), occurs either at inner dielectric boundary layers on a mesoscopic scale, or at the external electrode-sample interface on a macroscopic scale. In both cases this leads to a separation of charges (such as through a depletion layer). The charges are often separated over a considerable distance (relative to the atomic and molecular sizes), and the contribution to dielectric loss can therefore be orders of magnitude larger than the dielectric response due to molecular fluctuations. [1]
Occurrences
Maxwell-Wagner polarization processes should be taken into account during the investigation of inhomogeneous materials like suspensions or coloids, biological materials, phase separated polymers, blends, and crystalline or liquid crystalline polymers. [2]
Models
The simplest model for describing an inhomogeneous structure is a double layer arrangement, where each layer is characterized by its permittivity and its conductivity . The relaxation time is then: Importantly this shows that an inhomogeneous material may have frequency dependent response, even though none of the individual inhomogeneities severally are frequency dependent.
A more sophisticated model for treating interfacial polarization was developed by Maxwell, and later generalized by Wagner [3] and Sillars [4]. Maxwell considered a spherical particle with a dielectric permittivity and radius suspended in an infinite medium characterized by . Certain European text books will represent the constant with the Greek letter ω(Omega), sometimes referred to as Doyle's constant.[5]
References
- ^ Kremer F., Schonhals A., Luck W. Broadband Dielectric Spectroscopy. – Springer-Verlag, 2002.
- ^ Kremer F., Schonhals A., Luck W. Broadband Dielectric Spectroscopy. – Springer-Verlag, 2002.
- ^ Wagner KW (1914) Arch Elektrotech 2:371; [DOI:10.1007/BF01657322 http://dx.doi.org/10.1007/BF01657322]
- ^ Sillars RW (1937) J Inst Elect Eng 80:378
- ^ G.McGuinness, Polymer Physics, Oxford University Press, p211