In electromagnetism, the absolute permittivity, often simply called permittivity and denoted by the Greek letter ε (epsilon), is a measure of the electric polarizability of a dielectric. A material with high permittivity polarizes more in response to an applied electric field than a material with low permittivity, thereby storing more energy in the electric field. In electrostatics, the permittivity plays an important role in determining the capacitance of a capacitor.
More generally, the permittivity is a thermodynamic function of state . It can depend on the frequency, magnitude, and direction of the applied field. The SI unit for permittivity is farad per meter (F/m).
This dimensionless quantity is also often and ambiguously referred to as the permittivity. Another common term encountered for both absolute and relative permittivity is the dielectric constant which has been deprecated in physics and engineering as well as in chemistry.
By definition, a perfect vacuum has a relative permittivity of exactly 1 whereas at STP, air has a relative permittivity of κair = 1.0006.
Relative permittivity is directly related to electric susceptibility (χ) by
otherwise written as
- 1 Units
- 2 Explanation
- 3 Vacuum permittivity
- 4 Relative permittivity
- 5 Practical applications
- 6 Dispersion and causality
- 7 Measurement
- 8 See also
- 9 Notes
- 10 References
- 11 Further reading
- 12 External links
The standard SI unit for permittivity is farad per meter (F/m or F·m−1).
In electromagnetism, the electric displacement field D represents how an electric field E influences the organization of electric 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
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 values.
In SI units, permittivity is measured in farads per meter (F/m or A2·s4·kg−1·m−3). The displacement field D is measured in units of coulombs per square meter (C/m2), while the electric field E is measured in volts per meter (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.
Its value is
The constants c0 and μ0 were defined in SI units to have exact numerical values until redefinition of SI units in 2019. (The approximation in the second value of ε0 above stems from π being an irrational number.)
The linear permittivity of a homogeneous material is usually given relative to that of free space, as a relative permittivity εr (also called dielectric constant, although this term is deprecated and sometimes only refers to the static, zero-frequency relative permittivity). In an anisotropic material, the relative permittivity may be a tensor, causing birefringence. The actual permittivity is then calculated by multiplying the relative permittivity by ε0:
where χ (frequently written χe) is the electric susceptibility of the material.
where ε0 is the electric permittivity of free space.
The susceptibility of a medium is related to its relative permittivity εr by
So in the case of a vacuum,
The electric displacement D is related to the polarization density P by
The capacitance of a capacitor is based on its design and architecture, meaning it will not change with charging and discharging. The formula for capacitance is written as
where is the area of one plate, is the distance between the plates, and is the permittivity of the medium between the two plates. For a capacitor with relative permittivity , it can be said that
where is the net electric flux passing through the surface, is the charge enclosed in the Gaussian surface, is the electric field vector at a given point on the surface, and is a differential area vector on the Gaussian surface.
If the Gaussian surface uniformly encloses an insulated, symmetrical charge arrangement, the formula can be simplified to
where represents the angle between the electric field vector and the area vector.
If all of the electric field lines cross the surface at 90°, the formula can be further simplified to
Because the surface area of a sphere is , the electric field a distance away from a uniform, spherical charge arrangement is
where is Coulomb's constant ( ). This formula applies to the electric field due to a point charge, outside of a conducting sphere or shell, outside of a uniformly charged insulating sphere, or between the plates of a spherical capacitor.
Dispersion and causalityEdit
In general, a material cannot polarize instantaneously in response to an applied field, and so the more general formulation as a function of time is
That is, the polarization is a convolution of the electric field at previous times with time-dependent susceptibility given by χ(Δt). The upper limit of this integral can be extended to infinity as well if one defines χ(Δt) = 0 for Δt < 0. An instantaneous response would correspond to a Dirac delta function susceptibility χ(Δt) = χδ(Δt).
This frequency dependence of the susceptibility leads to frequency dependence of the permittivity. The shape of the susceptibility with respect to frequency characterizes the dispersion properties of the material.
Moreover, the fact that the polarization can only depend on the electric field at previous times (i.e. effectively χ(Δt) = 0 for Δt < 0), a consequence of causality, imposes Kramers–Kronig constraints on the susceptibility χ(0).
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 change instantaneously when an electric field is applied. 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 of the (angular) frequency ω of the applied field:
(since complex numbers allow specification of magnitude and phase). The definition of permittivity therefore becomes
- D0 and E0 are the amplitudes of the displacement and electric fields, respectively,
- i is the imaginary unit, i2 = −1.
The response of a medium to static electric fields is described by the low-frequency limit of permittivity, also called the static permittivity εs (also εDC):
At the high-frequency limit (meaning optical frequencies), the complex permittivity is commonly referred to as ε∞ (or sometimes εopt). At the plasma frequency and below, dielectrics behave as ideal metals, with electron gas behavior. The static permittivity is a good approximation for alternating 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 field strength (E0), D and E remain proportional, and
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:
- ε′ is the real part of the permittivity;
- ε″ is the imaginary part of the permittivity;
- δ is the loss angle.
The choice of sign for time-dependence, e−iωt, 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 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 ε(ω) 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, ε″, 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 characterizes 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:
In this expression, Wc,v(E) represents the product of the Brillouin zone-averaged transition probability at the energy E with the joint density of states, Jc,v(E); φ is a broadening function, representing the role of scattering in smearing out the energy levels. In general, the broadening is intermediate between Lorentzian and Gaussian; for an alloy it is somewhat closer to Gaussian because of strong scattering from statistical fluctuations in the local composition on a nanometer scale.
According to the Drude model of magnetized plasma, a more general expression which takes into account the interaction of the carriers with an alternating electric field at millimeter and microwave frequencies in an axially magnetized semiconductor requires the expression of the permittivity as a non-diagonal tensor. (see also Electro-gyration).
If ε2 vanishes, then the tensor is diagonal but not proportional to the identity and the medium is said to be a uniaxial medium, which has similar properties to a uniaxial crystal.
Classification of materialsEdit
|εr″/||Current conduction||Field propagation|
|≪ 1||low-conductivity material
|≈ 1||lossy conducting material||lossy propagation medium|
|≫ 1||high-conductivity material
Materials can be classified according to their complex-valued permittivity ε, upon comparison of its real ε′ and imaginary ε″ components (or, equivalently, conductivity, σ, when accounted for in the latter). A perfect conductor has infinite conductivity, σ = ∞, while a perfect dielectric is a material that has no conductivity at all, σ = 0; this latter case, of real-valued permittivity (or complex-valued permittivity with zero imaginary component) is also associated with the name lossless media. Generally, when σ/ ≪ 1 we consider the material to be a low-loss dielectric (although not exactly lossless), whereas σ/ ≫ 1 is associated with a good conductor; such materials with non-negligible conductivity yield a large amount of loss that inhibit the propagation of electromagnetic waves, thus are also said to be lossy media. Those materials that do not fall under either limit are considered to be general media.
In the case of a lossy medium, i.e. when the conduction current is not negligible, the total current density flowing is:
- σ is the conductivity of the medium;
- ε′ is the real part of the permittivity.
- ε̂ is the complex permittivity
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:
- First are the 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 because of 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.
- Second are the 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.
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. Both of these resonances are at higher frequencies than the operating frequency of microwave ovens.
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).
At high frequencies (such as UV and above), molecules cannot relax, and the energy is purely absorbed by atoms, exciting electron energy levels. Thus, these frequencies are classified as ionizing radiation.
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 phenomenological model is accepted as being an adequate method of capturing experimental behaviors. The Debye model and the Lorentz model use a first-order and second-order (respectively) lumped system parameter linear representation (such as an RC and an LRC resonant circuit).
The relative permittivity 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 hertz. 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 excitation fields, a number of measurement setups are used, each adequate for a special frequency range.
- Low-frequency time domain measurements (10−6 to 103 Hz)
- Low-frequency frequency domain measurements (10−5 to 106 Hz)
- Reflective coaxial methods (106 to 1010 Hz)
- Transmission coaxial method (108 to 1011 Hz)
- Quasi-optical methods (109 to 1010 Hz)
- Terahertz time-domain spectroscopy (1011 to 1013 Hz)
- Fourier-transform methods (1011 to 1015 Hz)
At infrared and optical frequencies, a common technique is ellipsometry. Dual polarisation interferometry is also used to measure the complex refractive index for very thin films at optical frequencies.
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