Polarization density

From Wikipedia, the free encyclopedia
Jump to: navigation, search

In classical electromagnetism, polarization density (or electric polarization, or simply polarization) is the vector field that expresses the density of permanent or induced electric dipole moments in a dielectric material. When a dielectric is placed in an external electric field, its molecules gain electric dipole moment and the dielectric is said to be polarized. The electric dipole moment induced per unit volume of the dielectric material is called the electric polarization of the dielectric.[1][2]

Polarization density also describes how a material responds to an applied electric field as well as the way the material changes the electric field, and can be used to calculate the forces that result from those interactions. It can be compared to magnetization, which is the measure of the corresponding response of a material to a magnetic field in magnetism. The SI unit of measure is coulombs per square meter, and polarization density is represented by a vector P.[2]

Definition[edit]

An external electric field that is applied to a dielectric material, causes a displacement of bound charged elements. These are elements which are bound to molecules and are not free to move around the material. Positive charged elements are displaced in the direction of the field, and negative charged elements are displaced opposite to the direction of the field. The molecules may remain neutral in charge, yet an electric dipole moment forms.[3][4]

For a certain volume element in the material \Delta V, which carries a dipole moment \Delta\mathbf p, we define the polarization vector P:

\mathbf P = \frac{\Delta\mathbf p}{\Delta V}

In general, the dipole moment \Delta\mathbf p changes from point to point within the dielectric. Hence, the polarization density P of an infinitesimal change dp in the dipole moment for a given change dV in the volume is:

\mathbf P={\mathrm d\mathbf p \over \mathrm d V} \qquad (1)

The net charge appearing as a result of polarization is called bound charge and denoted Q_b.

Other Expressions[edit]

Let a volume dV be isolated inside the dielectric. Due to polarization the positive bound charge \mathrm d q_b^+ will be displaced a distance \mathbf d relative to the negative bound charge \mathrm d q_b^-, giving rise to a dipole moment  \mathrm d \mathbf p = \mathrm d q_b\mathbf d. Replacing this expression into (1) we get:

\mathbf P={\mathrm d q_b \over \mathrm d V}\mathbf d

Since the charge \mathrm d q_b bounded in the volume dV is equal to \rho_b \mathrm d V the equation for P becomes:[3]

\mathbf P = \rho_b \mathbf d \qquad (2)

where  \rho_b is the density of the bound charge in the volume under consideration.

Gauss's Law for the Field of P[edit]

For a given volume V enclosed by a surface S, the bound charge Q_b inside it is equal to the flux of P through S taken with the negative sign, or

-Q_b  = \oiint{\scriptstyle S}\mathbf{P} \cdot \mathrm{d}\mathbf{A} \qquad (3)

Differential Form[edit]

By the divergence theorem, Gauss's law for the field P can be stated in differential form as:

 -\rho_b = \nabla \cdot \mathbf P,

where ∇ · P is the divergence of the field P through a given surface containing the bound charge density \rho_b.

Relationship between the fields of P and E[edit]

Homogeneous, Isotropic Dielectrics[edit]

Field lines of the D-field in a dielectric sphere with greater susceptibility than its surroundings, placed in a previously-uniform field.[5] The field lines of the E-field are not shown: These point in the same directions, but many field lines start and end on the surface of the sphere, where there is bound charge. As a result, the density of E-field lines is lower inside the sphere than outside, which corresponds to the fact that the E-field is weaker inside the sphere than outside.

In a homogeneous linear and isotropic dielectric medium, the polarization is aligned with and proportional to the electric field E:[6]


\mathbf P= \chi\varepsilon_0 \mathbf E,

where ε0 is the electric constant, and χ is the electric susceptibility of the medium. Note that χ is just a scalar. This is a particular case due to the isotropy of the dielectric.

Taking into account this relation between P and E, equation (3) becomes:[3]

-Q_b  =  \chi\varepsilon_0\  \oiint{\scriptstyle S}\mathbf{E} \cdot \mathrm{d}\mathbf{A}

The expression in the integral is Gauss's law for the field E which yields the total charge, both free (Q_f) and bound (Q_b), in the volume V enclosed by S.[3] Therefore


\begin{align}
-Q_b &= \chi Q_{\mathrm{total}}\\
&= \chi (Q_f + Q_b)\\
Q_b &= -\frac{\chi}{1+ \chi}Q_f,
\end{align}

which can be written in terms of free charge and bound charge densities (by considering the relationship between the charges, their volume charge densities and the given volume):

\rho_b = -\frac{\chi}{1+ \chi}\rho_f

Since within a homogeneous dielectric there can be no free charges (\rho_f = 0), by the last equation it follows that there is no bulk bound charge in the material (\rho_b = 0). And since free charges can get as close to the dielectric as to its topmost surface, it follows that polarization only gives rise to surface bound charge density (denoted \sigma_b to avoid ambiguity with the volume bound charge density \rho_b).[3]

\sigma_b may be related to P by the following equation:[7]

\sigma_b = \mathbf P \cdot \mathbf{\hat{n}_{out}}

where \mathbf{\hat{n}_{out}} is the normal vector to the surface S pointing outwards.

Anisotropic Dielectrics[edit]

The class of dielectrics where the polarization density and the electric field are not in the same direction are known as anisotropic materials.

In such materials, the ith component of the polarization is related to the jth component of the electric field according to:[6]

P_i = \sum_j \epsilon_0 \chi_{ij} E_j , \,\!

This relation shows, for example, that a material can polarize in the x direction by applying a field in the z direction, and so on. The case of an anisotropic dielectric medium is described by the field of crystal optics.

As in most electromagnetism, this relation deals with macroscopic averages of the fields and dipole density, so that one has a continuum approximation of the dielectric materials that neglects atomic-scale behaviors. The polarizability of individual particles in the medium can be related to the average susceptibility and polarization density by the Clausius-Mossotti relation.

In general, the susceptibility is a function of the frequency ω of the applied field. When the field is an arbitrary function of time t, the polarization is a convolution of the Fourier transform of χ(ω) with the E(t). This reflects the fact that the dipoles in the material cannot respond instantaneously to the applied field, and causality considerations lead to the Kramers–Kronig relations.

If the polarization P is not linearly proportional to the electric field E, the medium is termed nonlinear and is described by the field of nonlinear optics. To a good approximation (for sufficiently weak fields, assuming no permanent dipole moments are present), P is usually given by a Taylor series in E whose coefficients are the nonlinear susceptibilities:

\frac{P_i}{\epsilon_0} = \sum_j  \chi^{(1)}_{ij} E_j  +  \sum_{jk} \chi_{ijk}^{(2)} E_j E_k + \sum_{jk\ell} \chi_{ijk\ell}^{(3)} E_j E_k E_\ell  + \cdots \!

where \chi^{(1)} is the linear susceptibility, \chi^{(2)} is the second-order susceptibility (describing phenomena such as the Pockels effect, optical rectification and second-harmonic generation), and \chi^{(3)} is the third-order susceptibility (describing third-order effects such as the Kerr effect and electric field-induced optical rectification).

In ferroelectric materials, there is no one-to-one correspondence between P and E at all because of hysteresis.

Polarization density in Maxwell's equations[edit]

The behavior of electric fields (E and D), magnetic fields (B, H), charge density (ρ) and current density (J) are described by Maxwell's equations in matter.

Relations between E, D and P[edit]

In terms of volume charge densities, the free charge density \rho_f is given by

\rho_f = \rho - \rho_b

where \rho is the total charge density. By considering the relationship of each of the terms of the above equation to the divergence of their corresponding fields (of the electric displacement field D, E and P in that order), this can be written as:[8]

\mathbf{D} = \varepsilon_0\mathbf{E} + \mathbf{P}.

Here ε0 is the electric permittivity of empty space. In this equation, P is the (negative of the) field induced in the material when the "fixed" charges, the dipoles, shift in response to the total underlying field E, whereas D is the field due to the remaining charges, known as "free" charges. In general, P varies as a function of E depending on the medium, as described later in the article. In many problems, it is more convenient to work with D and the free charges than with E and the total charge.[1]

Time-varying Polarization Density[edit]

When the polarization density changes with time, the time-dependent bound-charge density creates a polarization current density of

 \mathbf{J}_p = \frac{\partial \mathbf{P}}{\partial t}

so that the total current density that enters Maxwell's equations is given by

 \mathbf{J} = \mathbf{J}_f + \nabla\times\mathbf{M} + \frac{\partial\mathbf{P}}{\partial t}

where Jf is the free-charge current density, and the second term is the magnetization current density (also called the bound current density), a contribution from atomic-scale magnetic dipoles (when they are present).

Polarization ambiguity[edit]

Example of how the polarization density in a bulk crystal is ambiguous. (a) A solid crystal. (b) By pairing the positive and negative charges in a certain way, the crystal appears to have an upward polarization. (c) By pairing the charges differently, the crystal appears to have a downward polarization.

The polarization inside a solid is not, in general, uniquely defined: It depends on which electrons are paired up with which nuclei.[9] (See figure.) In other words, two people, Alice and Bob, looking at the same solid, may calculate different values of P, and neither of them will be wrong. Alice and Bob will agree on the microscopic electric field E in the solid, but disagree on the value of the displacement field \mathbf{D}=\varepsilon_0 \mathbf{E}+\mathbf{P}. They will both find that Gauss's law is correct (\nabla\cdot\mathbf{D}= \rho_f), but they will disagree on the value of \rho_f at the surfaces of the crystal. For example, if Alice interprets the bulk solid to consist of dipoles with positive ions above and negative ions below, but the real crystal has negative ions as the topmost surface, then Alice will say that there is a negative free charge at the topmost surface. (She might view this as a type of surface reconstruction).

On the other hand, even though the value of P is not uniquely defined in a bulk solid, variations in P are uniquely defined.[9] If the crystal is gradually changed from one structure to another, there will be a current inside each unit cell, due to the motion of nuclei and electrons. This current results in a macroscopic transfer of charge from one side of the crystal to the other, and therefore it can be measured with an ammeter (like any other current) when wires are attached to the opposite sides of the crystal. The time-integral of the current is proportional to the change in P. The current can be calculated in computer simulations (such as density functional theory); the formula for the integrated current turns out to be a type of Berry's phase.[9]

The non-uniqueness of P is not problematic, because every measurable consequence of P is in fact a consequence of a continuous change in P.[9] For example, when a material is put in an electric field E, which ramps up from zero to a finite value, the material's electronic and ionic positions slightly shift. This changes P, and the result is electric susceptibility (and hence permittivity). As another example, when some crystals are heated, their electronic and ionic positions slightly shift, changing P. The result is pyroelectricity. In all cases, the properties of interest are associated with a change in P.

Even though the polarization is in principle non-unique, in practice it is often (not always) defined by convention in a specific, unique way. For example, in a perfectly centrosymmetric crystal, P is usually defined by convention to be exactly zero. As another example, in a ferroelectric crystal, there is typically a centrosymmetric configuration above the Curie temperature, and P is defined there by convention to be zero. As the crystal is cooled below the Curie temperature, it shifts gradually into a more and more non-centrosymmetric configuration. Since gradual changes in P are uniquely defined, this convention gives a unique value of P for the ferroelectric crystal, even below its Curie temperature.

See also[edit]

References and notes[edit]

  1. ^ a b Introduction to Electrodynamics (3rd Edition), D.J. Griffiths, Pearson Education, Dorling Kindersley, 2007, ISBN 81-7758-293-3
  2. ^ a b McGraw Hill Encyclopaedia of Physics (2nd Edition), C.B. Parker, 1994, ISBN 0-07-051400-3
  3. ^ a b c d e Irodov, I.E.. Basic Laws of Electromagnetism. Mir Publishers, CBS Publishers & Distributors, 1986. ISBN 81-239-0306-5
  4. ^ Matveev. A. N.. Electricity and Magnetism. Mir Publishers. 1986.
  5. ^ Based upon equations from Andrew Gray (1888). The theory and practice of absolute measurements in electricity and magnetism. Macmillan & Co. pp. 126–127. , which refers to papers by Sir W. Thomson.
  6. ^ a b Feynman Lectures on Physics: Volume 2, R.P. Feynman, R.B. Leighton, M. Sands, Addison-Wesley, 1964, ISBN 0-201-02117-X
  7. ^ Electromagnetism (2nd Edition), I.S. Grant, W.R. Phillips, Manchester Physics, John Wiley & Sons, 2008, ISBN 978-0-471-92712-9
  8. ^ Saleh, B.E.A.; Teich, M.C. (2007). Fundamentals of Photonics. Hoboken, NJ: Wiley. p. 154. ISBN 978-0-471-35832-9. 
  9. ^ a b c d Resta, Raffaele (1994). "Macroscopic polarization in crystalline dielectrics: the geometric phase approach" (PDF). Rev. Mod. Phys. 66: 899. Bibcode:1994RvMP...66..899R. doi:10.1103/RevModPhys.66.899.  See also: D Vanderbilt, Berry phases and Curvatures in Electronic Structure Theory, an introductory-level powerpoint.