Permittivity

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Permittivity is a physical quantity that describes how an electric field affects and is affected by a dielectric medium, and is determined by the ability of a material to polarize in response to the field, and thereby reduce the total electric field inside the material. Thus, permittivity relates to a material's ability to transmit (or "permit") an electric field.

It is directly related to electric susceptibility. For example, in a capacitor, an increased permittivity allows the same charge to be stored with a smaller electric field (and thus a smaller voltage), leading to an increased capacitance.

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[edit] Explanation

In electromagnetism, the electric displacement field D represents how an electric field E influences the organization of electrical charges in a given medium, including charge migration and electric dipole reorientation. Its relation to permittivity in the very simple case of linear, homogeneous, isotropic materials with instantaneous response to changes in electric field is

\mathbf{D}=\varepsilon \mathbf{E}

where the permittivity ε is a scalar. If the medium is not isotropic, the permittivity is a second rank tensor.

In general, permittivity isn't a constant, as it can vary with the position in the medium, the frequency of the field applied, humidity, temperature, and other parameters. In a nonlinear medium, the permittivity can depend on the strength of the electric field. Permittivity as a function of frequency can take on real or complex values.

In SI units, permittivity is measured in farads per metre (F/m). The displacement field D is measured in units of coulombs per square metre (C/m2), while the electric field E is measured in volts per metre (V/m). D and E describe the interaction between charged objects. D is related to the charge densities associated with this interaction, while E is related to the forces and potential differences.

[edit] Vacuum permittivity

Main article: vacuum permittivity

Vacuum permittivity \varepsilon_{0} (also called permittivity of free space or the electric constant) is the ratio D/E in free space.

\varepsilon_0 \ \stackrel{\mathrm{def}}{=}\ \frac{1}{{c}^2\mu_0} \approx 8.8541878176… × 10−12 F/m (or C2N-1m-2),
c (or c0) is the speed of light in free space.[1]
μ0 is the magnetic constant.

Constants c and μ0 are defined in SI units to have exact numerical values (see NIST), shifting responsibility of experiment to the determination of the meter and the ampere. (The approximation in the value of ε0 stems from π being an irrational number.) The electric constant ε0 also appears in Coulomb's law as a part of the Coulomb force constant, 1 / ( 4π ε0 ), which expresses the force between two unit charges separated by unit distance in vacuum.

The linear permittivity of a homogeneous material is usually given relative to that of free space, as a relative permittivity \varepsilon_{r} (also called dielectric constant, although this sometimes only refers to the static, zero-frequency relative permittivity). In an anisotropic material, the relative permittivity may be a tensor. The actual permittivity is then calculated by multiplying the relative permittivity by \varepsilon_{0}:

\varepsilon = \varepsilon_r \varepsilon_0 = (1+\chi_e)\varepsilon_0

where

\,\chi_e is the electric susceptibility of the material.

[edit] Permittivity in media

In the common case of isotropic media, D and E are parallel vectors and \varepsilon is a scalar, but in general anisotropic media this is not the case and \varepsilon is a rank-2 tensor (causing birefringence). The permittivity \varepsilon and magnetic permeability μ of a medium together determine the phase velocity v of electromagnetic radiation through that medium:

\varepsilon \mu = \frac{1}{v^2}.

When an external electric field is applied to a real medium, a current flows. The total current flowing within the medium consists of two parts: a conduction and a displacement current. The displacement current can be thought of as the elastic response of the material to the applied electric field. As the magnitude of the externally applied electric field is increased, an increasing amount of energy is stored in the electric displacement field within the material. If the electric field is subsequently decreased, the material will release the stored electrostatic energy. The displacement current reflects the resulting change in electrostatic energy stored within the material. The electric displacement can be separated into a vacuum contribution and one arising from the material by

\mathbf{D} = \varepsilon_{0} \mathbf{E} + \mathbf{P} = \varepsilon_{0} \mathbf{E} + \varepsilon_{0}\chi\mathbf{E} = \varepsilon_{0} \mathbf{E} \left( 1 + \chi \right),

where

P is the polarization of the medium
χ its electric susceptibility.

It follows that the relative permittivity and susceptibility of a sample are related, \varepsilon_{r} = \chi + 1.

[edit] Complex permittivity

A dielectric permittivity spectrum over a wide range of frequencies. ε′ and ε″ denote the real and the imaginary part of the permittivity, respectively. Various processes are labeled on the image: ionic and dipolar relaxation, and atomic and electronic resonances at higher energies. From the Dielectric spectroscopy page [1] of the research group of Dr. Kenneth A. Mauritz.
A dielectric permittivity spectrum over a wide range of frequencies. ε′ and ε″ denote the real and the imaginary part of the permittivity, respectively. Various processes are labeled on the image: ionic and dipolar relaxation, and atomic and electronic resonances at higher energies. From the Dielectric spectroscopy page [1] of the research group of Dr. Kenneth A. Mauritz.

As opposed to the response of a vacuum, the response of normal materials to external fields generally depends on the frequency of the field. This frequency dependence reflects the fact that a material's polarization does not respond instantaneously to an applied field. The response must always be causal (arising after the applied field) which can be represented by a phase difference. For this reason permittivity is often treated as a complex function (since complex numbers allow specification of magnitude and phase) of the frequency of the applied field ω, \varepsilon \rightarrow \widehat{\varepsilon}(\omega). The definition of permittivity therefore becomes

D_{0}e^{-i \omega t} = \widehat{\varepsilon}(\omega) E_{0} e^{-i \omega t},

where

D0 and E0 are the amplitudes of the displacement and electrical fields, respectively,
i 2 = −1 is the imaginary unit.

It is important to realise that the choice of sign for time-dependence dictates the sign convention for the imaginary part of permittivity. The signs used here correspond to those commonly used in physics, whereas for the engineering convention one should reverse all imaginary quantities.

The response of a medium to static electric fields is described by the low-frequency limit of permittivity, also called the static permittivity \varepsilon_{s} (also \varepsilon_{DC}):

\varepsilon_{s} = \lim_{\omega \rightarrow 0} \widehat{\varepsilon}(\omega).

At the high-frequency limit, the complex permittivity is commonly referred to as ε∞. At the plasma frequency and above, dielectrics behave as ideal metals, with electron gas behavior. The static permittivity is a good approximation for altering fields of low frequencies, and as the frequency increases a measurable phase difference δ emerges between D and E. The frequency at which the phase shift becomes noticeable depends on temperature and the details of the medium. For moderate fields strength (E0), D and E remain proportional, and

\widehat{\varepsilon} = \frac{D_0}{E_0}e^{i\delta} = |\varepsilon|e^{i\delta}.

Since the response of materials to alternating fields is characterized by a complex permittivity, it is natural to separate its real and imaginary parts, which is done by convention in the following way:

\widehat{\varepsilon}(\omega) = \varepsilon'(\omega) + i\varepsilon''(\omega) = \frac{D_0}{E_0} \left( \cos\delta + i\sin\delta \right).

where

\varepsilon'' is the imaginary part of the permittivity, which is related to the dissipation (or loss) of energy within the medium.
\varepsilon' is the real part of the permittivity, which is related to the stored energy within the medium.

The complex permittivity is usually a complicated function of frequency ω, since it is a superimposed description of dispersion phenomena occurring at multiple frequencies. The dielectric function \varepsilon(\omega) must have poles only for frequencies with positive imaginary parts, and therefore satisfies the Kramers–Kronig relations. However, in the narrow frequency ranges that are often studied in practice, the permittivity can be approximated as frequency-independent or by model functions.

At a given frequency, the imaginary part of \widehat{\varepsilon} leads to absorption loss if it is positive (in the above sign convention) and gain if it is negative. More generally, the imaginary parts of the eigenvalues of the anisotropic dielectric tensor should be considered.

In the case of solids, the complex dielectric function is intimately connected to band structure. The primary quantity that characterize the electronic structure of any crystalline material is the probability of photon absorption, which is directly related to the imaginary part of the optical dielectric function ε(ω). The optical dielectric function is given by the fundamental expression:[2]

\epsilon(\omega)=1+\frac{8\pi^2e^2}{m^2}\sum_{c,v}\int_{}^{} W_{cv}(E) \left[ \phi (\hbar \omega - E)-\phi( \hbar \omega +E) \right ] \, dx \ .

In this expression, Wcv ( E ) represents the product of the Brillouin zone-averaged transition probability at the energy E with the joint density of states,[3][4] Jcv ( E ); φ is a broadening function, representing the role of scattering in smearing out the energy levels.[5] In general, the broadening is intermediate between Lorentzian and Gaussian;[6][7] for an alloy it is somewhat closer to Gaussian because of strong scattering from statistical fluctuations in the local composition on a nanometer scale.

[edit] Classification of materials

Materials can be classified according to their permittivity and conductivity, σ. Materials with a large amount of loss inhibit the propagation of electromagnetic waves. In this case, generally when \frac{\sigma}{\omega\varepsilon}\gg1, we consider the material to be a good conductor. Dielectrics are associated with lossless or low-loss materials, where \frac{\sigma}{\omega\varepsilon}\ll1. Those that do not fall under either limit are considered to be general media. A perfect dielectric is a material that has no conductivity, thus exhibiting only a displacement current. Therefore it stores and returns electrical energy as if it were an ideal capacitor.

[edit] Lossy medium

In the case of lossy medium, i.e. when the conduction current is not negligible, the total current density flowing is:

J_{tot} = J_c + J_d = \sigma E - i \omega \varepsilon E = -i \omega \widehat{\varepsilon} E

where

σ is the conductivity of the medium;
ε is the real part of the permittivity.
\widehat{\varepsilon} is the complex permittivity

The size of the displacement current is dependent on the frequency ω of the applied field E; there is no displacement current in a constant field.

In this formalism, the complex permittivity is defined as:

\widehat{\varepsilon} = \varepsilon + i \frac{\sigma}{\omega}

In general, the absorption of electromagnetic energy by dielectrics is covered by a few different mechanisms that influence the shape of the permittivity as a function of frequency:

  • Relaxation effects associated with permanent and induced molecular dipoles. At low frequencies the field changes slowly enough to allow dipoles to reach equilibrium before the field has measurably changed. For frequencies at which dipole orientations cannot follow the applied field due to the viscosity of the medium, absorption of the field's energy leads to energy dissipation. The mechanism of dipoles relaxing is called dielectric relaxation and for ideal dipoles is described by classic Debye relaxation.
  • Resonance effects, which arise from the rotations or vibrations of atoms, ions, or electrons. These processes are observed in the neighborhood of their characteristic absorption frequencies.

The above effects often combine to cause non-linear effects within capacitors. For example, dielectric absorption refers to the inability of a capacitor that has been charged for a long time to completely discharge when briefly discharged. Although an ideal capacitor would remain at zero volts after being discharged, real capacitors will develop a small voltage, a phenomenon that is also called soakage or battery action. For some dielectrics, such as many polymer films, the resulting voltage may be less than 1-2% of the original voltage. However, it can be as much as 15 - 25% in the case of electrolytic capacitors or supercapacitors.

[edit] Quantum-mechanical interpretation

In terms of quantum mechanics, permittivity is explained by atomic and molecular interactions.

At low frequencies, molecules in polar dielectrics are polarized by an applied electric field, which induces periodic rotations. For example, at the microwave frequency, the microwave field causes the periodic rotation of water molecules, sufficient to break hydrogen bonds. The field does work against the bonds and the energy is absorbed by the material as heat. This is why microwave ovens work very well for materials containing water. There are two maxima of the imaginary component (the absorptive index) of water, one at the microwave frequency, and the other at far ultraviolet (UV) frequency.

At moderate frequencies, the energy is too high to cause rotation, yet too low to affect electrons directly, and is absorbed in the form of resonant molecular vibrations. In water, this is where the absorptive index starts to drop sharply, and the minimum of the imaginary permittivity is at the frequency of blue light (optical regime). This is why water is blue, and also why sunlight does not damage water-containing organs such as the eye.[2]

At high frequencies (such as UV and above), molecules cannot relax, and the energy is purely absorbed by atoms, exciting electron energy levels.

While carrying out a complete ab initio (that is, first-principles) modelling is now computationally possible, it has not been widely applied yet. Thus, a phenomological model is accepted as being an adequate method of capturing experimental behaviors. The Debye model and the Lorentz model use a 1st-order and 2nd-order (respectively) lumped system parameter linear representation (such as an RC and an LRC resonant circuit).

[edit] Measurement

The dielectric constant of a material can be found by a variety of static electrical measurements. The complex permittivity is evaluated over a wide range of frequencies by using different variants of dielectric spectroscopy, covering nearly 21 orders of magnitude from 10−6 to 1015 Hz. Also, by using cryostats and ovens, the dielectric properties of a medium can be characterized over an array of temperatures. In order to study systems for such diverse exciting fields, a number of measurement setups are used, each adequate for a special frequency range.

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Further information might be found on the talk page or at requests for expansion.


  • Low-frequency time domain measurements (10−6−103 Hz)
  • Low-frequency frequency domain measurements (10−5−106 Hz)
  • Reflective coaxial methods (106−1010 Hz)
  • Transmission coaxial method (108−1011 Hz)
  • Quasi-optical methods (109−1010 Hz)
  • Fourier-transform methods (1011−1015 Hz)

[edit] References and notes

  1. ^ Current practice of international standards organizations such as NIST and BIPM is to use c0 to denote the speed of light in vacuum according to ISO 31. In the original Recommendation of 1983, the symbol c was used for this purpose. See NIST Special Publication 330, Appendix 2, p. 45
  2. ^ Peter Y. Yu, Manuel Cardona (2001). Fundamentals of Semiconductors: Physics and Materials Properties. Berlin: Springer, pp. 261 ff. ISBN 3540254706. 
  3. ^ José García Solé, Jose Solé, Luisa Bausa, (2001). An introduction to the optical spectroscopy of inorganic solids. Wiley, Appendix A1, pp, 263ff. ISBN 0470868856. 
  4. ^ John H. Moore, Nicholas D. Spencer (2001). Encyclopedia of chemical physics and physical chemistry. Taylor and Francis, pp. 105 ff. ISBN 0750307986. 
  5. ^ Solé and Bausa, pp. 10 ff. ISBN 3540254706. 
  6. ^ Hartmut Haug, Stephan W. Koch (1994). Quantum Theory of the Optical and Electronic Properties of Semiconductors. World Scientific, pp. 196 ff. ISBN 9810218648. 
  7. ^ Manijeh Razeghi (2006). Fundamentals of Solid State Engineering. Birkhauser, pp. 383 ff. ISBN 0387281525. 

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