In dielectric spectroscopy, large frequency dependent contributions to the dielectric response, especially at low frequencies, may come from build-ups of charge. This 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]
Maxwell-Wagner polarization processes should be taken into account during the investigation of inhomogeneous materials like suspensions or colloids, biological materials, phase separated polymers, blends, and crystalline or liquid crystalline polymers.[2]
The simplest model for describing an inhomogeneous structure is a double layer arrangement, where each layer is characterized by its permittivity
\epsilon'1,\epsilon'2
\sigma1,\sigma2
\tauMW
=\epsilon | ||||
|
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
\epsilon'2
R
\epsilon1
\epsilon1