Permittivity

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 in a parallel plate capacitor is written as

${\displaystyle C=\varepsilon \ {\frac {A}{d}}}$

where ${\displaystyle A}$ is the area of one plate, ${\displaystyle d}$ is the distance between the plates, and ${\displaystyle \varepsilon }$ is the permittivity of the medium between the two plates. For a capacitor with relative permittivity ${\displaystyle \kappa }$, it can be said that

${\displaystyle C=\kappa \ \varepsilon _{0}{\frac {A}{d}}}$

Permittivity is connected to electric flux (and by extension electric field) through Gauss's law. Gauss's law states that for a closed Gaussian surface, S,

${\displaystyle \Phi _{E}={\frac {Q_{\text{enc}}}{\varepsilon _{0}}}=\oint _{S}\mathbf {E} \cdot \mathrm {d} \mathbf {A} ,}$

where ${\displaystyle \Phi _{E}}$ is the net electric flux passing through the surface, ${\displaystyle Q_{\text{enc}}}$ is the charge enclosed in the Gaussian surface, ${\displaystyle \mathbf {E} }$ is the electric field vector at a given point on the surface, and ${\displaystyle \mathrm {d} \mathbf {A} }$ 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

${\displaystyle EA\cos(\theta )={\frac {Q_{\text{enc}}}{\varepsilon _{0}}},}$

where ${\displaystyle \theta }$ represents the angle between the electric field lines and the normal (perpendicular) to S.

If all of the electric field lines cross the surface at 90°, the formula can be further simplified to

${\displaystyle E={\frac {Q_{\text{enc}}}{\varepsilon _{0}A}}.}$

Because the surface area of a sphere is ${\displaystyle 4\pi r^{2}}$, the electric field a distance ${\displaystyle r}$ away from a uniform, spherical charge arrangement is

${\displaystyle E={\frac {Q}{\varepsilon _{0}A}}={\frac {Q}{\varepsilon _{0}\left(4\pi r^{2}\right)}}={\frac {Q}{4\pi \varepsilon _{0}r^{2}}}.}$

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.

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.[10]

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:

${\displaystyle \varepsilon \rightarrow {\hat {\varepsilon }}(\omega )}$

(since complex numbers allow specification of magnitude and phase). The definition of permittivity therefore becomes

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

where

• 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 ε_s (also ε_DC):

${\displaystyle \varepsilon _{\mathrm {s} }=\lim _{\omega \rightarrow 0}{\hat {\varepsilon }}(\omega ).}$

At the high-frequency limit (meaning optical frequencies), the complex permittivity is commonly referred to as ε_∞ (or sometimes ε_opt[11]). 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

${\displaystyle {\hat {\varepsilon }}={\frac {D_{0}}{E_{0}}}=|\varepsilon |e^{-i\delta }.}$

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:

${\displaystyle {\hat {\varepsilon }}(\omega )=\varepsilon '(\omega )-i\varepsilon ''(\omega )=\left|{\frac {D_{0}}{E_{0}}}\right|\left(\cos \delta -i\sin \delta \right).}$

where

• 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:[12]

${\displaystyle \varepsilon (\omega )=1+{\frac {8\pi ^{2}e^{2}}{m^{2}}}\sum _{c,v}\int W_{c,v}(E){\bigl (}\varphi (\hbar \omega -E)-\varphi (\hbar \omega +E){\bigr )}\,dx.}$

In this expression, W_c,v(E) represents the product of the Brillouin zone-averaged transition probability at the energy E with the joint density of states,[13][14] J_c,v(E); φ is a broadening function, representing the role of scattering in smearing out the energy levels.[15] In general, the broadening is intermediate between Lorentzian and Gaussian;[16][17] 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.[18] (see also Electro-gyration).

${\displaystyle \mathbf {D} (\omega )={\begin{vmatrix}\varepsilon _{1}&-i\varepsilon _{2}&0\\i\varepsilon _{2}&\varepsilon _{1}&0\\0&0&\varepsilon _{z}\\\end{vmatrix}}\operatorname {\mathbf {E} } (\omega )}$

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.

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.[19] Generally, when σ/ωε′ ≪ 1 we consider the material to be a low-loss dielectric (although not exactly lossless), whereas σ/ωε′ ≫ 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:

${\displaystyle J_{\text{tot}}=J_{\mathrm {c} }+J_{\mathrm {d} }=\sigma E+i\omega \varepsilon 'E=i\omega {\hat {\varepsilon }}E}$

where

• σ is the conductivity of the medium;
• ${\displaystyle \varepsilon '=\varepsilon _{0}\varepsilon _{r}}$ is the real part of the permittivity.
• ${\displaystyle {\hat {\varepsilon }}=\varepsilon '-i\varepsilon ''}$is the complex permittivity

Note that this is using the electrical engineering convention of the Complex conjugate ambiguity; the physics/chemistry convention involves the complex conjugate of these equations.

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:[20][21]

${\displaystyle {\hat {\varepsilon }}=\varepsilon '\left(1-i{\frac {\sigma }{\omega \varepsilon '}}\right)=\varepsilon '-i{\frac {\sigma }{\omega }}}$

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:

• 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.

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. 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).