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 colloids, 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., & Schönhals A. (eds.): Broadband Dielectric Spectroscopy. – Springer-Verlag, 2003, ISBN 978-3-540-43407-8.
- ↑ Kremer F., & Schönhals A. (eds.): Broadband Dielectric Spectroscopy. – Springer-Verlag, 2003, ISBN 978-3-540-43407-8.
- ↑ Wagner KW (1914) Arch Elektrotech 2:371; doi:10.1007/BF01657322
- ↑ Sillars RW (1937) J Inst Elect Eng 80:378
- ↑ G.McGuinness, Polymer Physics, Oxford University Press, p211