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 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.
Explanation
In electromagnetism, 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 is
- [\mathbf=\varepsilon \cdot \mathbf]
In general, permittivity is not 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 value.
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 represent the same phenomenon, namely, 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.
Vacuum permittivity
Vacuum permittivity [\varepsilon_] (also called permittivity of free space) is the ratio D/E in vacuum.
where [c] is the speed of light and [\mu_0] is the permeability of vacuum. All three of these constants are exactly defined in SI units.
Vacuum permittivity also appears in Coulomb's law as a part of the Coulomb force constant, [\frac ], which expresses the attraction between two unit charges in vacuum.
The permittivity of a material is usually given relative to that of vacuum, as a relative permittivity [\varepsilon_] (also called dielectric constant). The actual permittivity is then calculated by multiplying the relative permittivity by [\varepsilon_]:
- [\varepsilon = \varepsilon_r \varepsilon_0 = (1+\chi_e)\varepsilon_0 ]
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 [\mu] of a medium together determine the phase velocity v of electromagnetic radiation through that medium:
- [\varepsilon \mu = \frac]
- [\mathbf = \varepsilon_ \mathbf + \mathbf = \varepsilon_ \mathbf + \varepsilon_\chi\mathbf = \varepsilon_ \mathbf \left( 1 + \chi \right),]
Complex permittivity
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). For this reason permittivity is often treated as a complex function of the frequency of the applied field [\omega], [\varepsilon \rightarrow \widehat(\omega)]. The definition of permittivity therefore becomes
- [D_e^ = \widehat(\omega) E_ e^,]
- [\varepsilon_ = \lim_ \widehat(\omega).]
- [\widehat = \frace^ = |\varepsilon|e^.]
- [\widehat(\omega) = \varepsilon'(\omega) + i\varepsilon''(\omega) = \frac \left( \cos\delta + i\sin\delta \right). ]
The complex permittivity is usually a complicated function of frequency ω, since it is a sumperimposed 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] 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.
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\gg1], we consider the material to be a good conductor. Dielectrics are associated with lossless or low-loss materials, where [\frac\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. In the case of lossy medium, i.e. when the conduction current is not negligible, the total current density flowing is:
- [ J_ = J_c + J_d = \sigma E + i \omega \varepsilon_0 \varepsilon_r E = i \omega \varepsilon_0 \widehat E ]
- σ is the conductivity of the medium;
- εr is the relative permittivity.
In this formalism, the complex permittivity [\widehat] is defined as:
- [ \widehat = \varepsilon_r + i \frac ]
Dielectric absorption processes
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.
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 high frequencies (such as UV and above), molecules cannot relax, and the energy is purely absorbed by atoms, exciting electron energy levels. At the plasma frequency, electrons are fully ionized, and conduct electricity.
At moderate frequencies, the energy is too low to affect electrons directly, yet too high to cause rotation, 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.
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).
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.
- Low-frequency time domain measurements (10−6−103 Hz)
- Low-frequency frequency domain measurements (10−5&mius;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)
See also
Suggested readings
- Theory of Electric Polarization: Dielectric Polarization, C.J.F. Böttcher, ISBN 0-44441-579-3
- Dielectrics and Waves edited by A. von Hippel, Arthur R., ISBN 0-89006-803-8
External links
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