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The effective electric charge associated with electric polarization is bound charge. For polarization density $\mathbf{P}$, its volume charge density is ${\rho }_{\mathrm{b}}=-\nabla \cdot \mathbf{P}$. At a boundary with unpolarized surroundings, its surface charge density is ${\sigma }_{\mathrm{b}}=\mathbf{P}\cdot \mathbf{n}$, where $\mathbf{n}$ is the outward unit normal vector.

A dielectric is a material in which an electric field produces electric polarization while transport of electric charge is sufficiently small for the intended use. An insulating solid in a capacitor is an example; real dielectrics can still have dielectric loss and nonzero electrical conductivity.

The important distinction is between rearranging bound electric charge and transporting mobile charge carriers through the specimen. Bound electric charges can move a little within a chemical atom or molecule, or an existing electric dipole can turn. Their averaged electric dipole moments produce electric polarization even if there is negligible steady electric current between the electrodes. A changing electric polarization does give a bound current; the absence of steady conduction does not mean that the material is electrically unresponsive.^[ref]

For uniform electric polarization $\mathbf{P}=P\hat{\mathbf{x}}$ in a rectangular slab, polarization density gives zero bound volume charge density in the interior and opposite bound surface charge densities $-P,+P$ on the left and right faces. The electric charge has been redistributed, not created. More generally, the divergence theorem makes the cancellation explicit:Here $\mathbf{n}$ is the outward normal vector on the material boundary. This accounts for both bound volume charge density and bound surface charge density; omitting either can falsely suggest that an initially neutral dielectric acquired net electric charge.

An electrical insulator between capacitor plates supports a useful combination: appreciable electric polarization, little leakage electric current, and tolerance of the intended electric field. This lets a small parallel-plate capacitor store separated electric charge and recoverable capacitor energy. The comparison in dielectric capacitor response explains why specifying fixed electric charge or fixed electric potential difference changes the answer. High relative permittivity alone does not establish good insulation or a large usable energy density; dielectric loss and dielectric breakdown matter as well.

The secondary pyroelectric effect is the change of polarization density produced when thermal strain acts through piezoelectricity. It is additional to the primary change at fixed strain. A linear constitutive description along the polar axis iswhere $e_{3j}$ are piezoelectric stress coefficients and ${\alpha }_j$ the freely developing thermal strains per kelvin. Thermal-expansion mismatch with a support or a deliberately chosen compliant structure can change the secondary contribution. It enhances the total response only if its sign reinforces the primary response; mechanical boundary conditions and thermal cycling must be characterized rather than assuming every restraint is beneficial.

Preventing axial expansion removes the free axial-strain contribution, but does not automatically eliminate every secondary contribution. In a one-dimensional idealization with only ${\epsilon }_3$ coupling and perfect axial clamping, that strain-mediated term vanishes. A real rod may still expand transversely, and nonzero $e_{31}$ or $e_{32}$ can change $P_3$ through those strains. In a stress-based constitutive equation, the same restraint appears as thermal stress and a piezoelectric term; do not add it a second time to a coefficient already specified for the constrained condition. Full suppression of all relevant thermal strains leaves the primary coefficient at fixed strain. The answer therefore depends on which degrees of freedom are constrained, not simply on the word “nanorod”.

For electrode area $A$, the change in spontaneous polarization density supplies a charge scale $\Delta Q=pA\Delta T$, while the film's capacitance is $C=\epsilon A/d$. The voltage magnitude is therefore $|\Delta V|=|p|d|\Delta T|/\epsilon$. More explicitly, for an initially compensated film with no change in free electrode charge, $\Delta D=\epsilon \Delta E+p\Delta T=0$. Taking $z$ from the lower electrode to the upper one gives $\Delta V_{\mathrm{upper}-\mathrm{lower}}=-d\Delta E=pd\Delta T/\epsilon$.The measurable magnitude is $0.339\mathrm{V}$, with polarity reversed by reversing the poling direction or the temperature change. This is an ideal open-circuit estimate: leakage, the measuring instrument's input capacitance and finite charge-relaxation time can reduce or reshape the observed voltage.

Polarization density $\mathbf{P}$ is electric dipole moment per unit volume. Displacing positive and negative bound charges leaves the bulk nearly neutral locally but can produce uncompensated charge where polarization varies or terminates. For a dielectric occupying a volume with outward unit normal $\mathbf{n}$,The divergence theorem makes their total sum zero for a body described entirely by bound dipoles. Uniform polarization gives no interior volume charge but generally gives opposite surface charges on different faces.

In a linear isotropic dielectric, $\mathbf{P}={ϵ}_0{\chi }_e\mathbf{E}$ and $\mathbf{D}={ϵ}_0\mathbf{E}+\mathbf{P}=ϵ\mathbf{E}$. Gauss's law becomes $\nabla \cdot \mathbf{D}={\rho }_f$, separating free from bound charge. Across a static interface, tangential electric field is continuous, while the normal displacement jumps by the free surface charge. Polarization charges alter the internal field, as in the dielectric cylinder calculation. Molecular distortion and orientation contribute differently, and response can depend on temperature and frequency. Bound charge is a redistribution of material charge, not an additional free-charge reservoir.

In electrostatics, the Maxwell equations in matter areHere ${\rho }_f$ is free charge density and $\mathbf{P}$ is polarization density. For a homogeneous isotropic linear dielectric, the constitutive equation is $\mathbf{D}={ϵ}_0{ϵ}_r\mathbf{E}$. Integrating the first equation over a thin pillbox straddling an interface, with unit normal $\mathbf{n}$ from medium 1 to medium 2, gives $\mathbf{n}\cdot ({\mathbf{D}}_2-{\mathbf{D}}_1)={\sigma }_f$. Integrating the second around a vanishingly narrow rectangular loop gives $\mathbf{n}\times ({\mathbf{E}}_2-{\mathbf{E}}_1)=0$. These are the electrostatic interface boundary conditions. When there is no free surface electric charge, the normal electric displacement field and tangential electric field are continuous; the normal electric field generally is not.

Neglect end fringing field of a capacitor. In either axial segment of the coaxial cylindrical capacitor, a cylindrical Gaussian surface gives $D_r={\lambda }_f/(2\pi r)$, where ${\lambda }_f$ is free electric charge per length. Integrating the radial electric field between the conductors givesThe liquid and air segments share the same conductor electric potential difference, so their capacitances add in parallel. Thus the partially filled coaxial capacitor hasHere the question's $ϵ$ is relative permittivity, and air's relative permittivity is approximated by one.

Write $x$ for the rise above the external level. The wide reservoir keeps that level approximately fixed. At constant applied voltage, one must include work done by the source: the appropriate electrical contribution to the mechanical potential is $-C{V}^2/2$. The upward dielectric insertion force at fixed voltage is consequentlyThe excess hydrostatic pressure $\rho gx$ acts over the annular area $A=\pi (b^2-a^2)$. Alternatively its gravitational potential energy is $\rho gA{x}^2/2$, since liquid initially at the reservoir level must be raised through all heights from zero to $x$. Balancing the derivatives givesThis assumes $h+x<L$, a communicating liquid reservoir, negligible capillarity, and a sufficiently long capacitor that end effects are small. Differentiating gives the dielectric-rise voltmeter's sensitivity at a bias $V$:To obtain its numerical value in $\mu \mathrm{m}{\mathrm{V}}^{-1}$, multiply the right-hand side in SI units by $10^6$. A convenient parametric scale, with $\beta =b/a$, isFor a concrete estimate, choose $a=1\mathrm{mm}$, $b=2\mathrm{mm}$, mass density $\rho =10^3\mathrm{kg}{\mathrm{m}}^{-3}$, relative permittivity $ϵ=2$ and operating voltage $V=100\mathrm{V}$. These are illustrative choices, not supplied apparatus data. They giveThus this millimetre-scale example requires fine optical displacement measurement for volt-level changes. The parametric formula states exactly how the estimate changes with the chosen geometry, liquid and bias.

The displacement is quadratic in voltage, cannot distinguish its sign, and has zero first-order sensitivity at zero bias. Smaller gaps and larger relative permittivity increase sensitivity, but capillarity, leakage, dielectric breakdown, temperature-dependent liquid properties, and finite available rise then limit performance. A nonconducting liquid avoids a sustained conduction load, although charging still draws electric charge and leakage is possible. A high voltage can give a readable displacement; a low-voltage instrument would require fine displacement measurement and careful calibration.

An electric dipole consists of equal and opposite electric charges separated by a displacement $\mathbf{d}$. Its electric dipole moment is $\mathbf{p}=q\mathbf{d}$, directed from negative to positive electric charge. At distances large compared with the separation, its leading electric potential and electric field areThere is no monopole term because the net electric charge is zero. The axial electric field points along $\mathbf{p}$ with magnitude $2p/(4\pi {ϵ}_0{r}^3)$, while the equatorial electric field points oppositely with half that magnitude.

A uniform applied electric field exerts zero net force on an ideal fixed electric dipole, but it exerts torque $\mathbf{\tau }=\mathbf{p}\times \mathbf{E}$. Its orientation-dependent potential energy is $U=-\mathbf{p}\cdot \mathbf{E}$, so alignment with the electric field is stable. A nonuniform applied electric field can also exert a net force, $\mathbf{F}=\nabla (\mathbf{p}\cdot \mathbf{E})$ for a fixed permanent electric dipole moment.

A permanent electric dipole moment exists without an applied electric field. An induced electric dipole moment instead develops in response to the local electric field; in an isotropic linear model $\mathbf{p}=\alpha \mathbf{E}$. Creating that induced moment requires accounting for the work of polarization, so its mechanical potential energy in a specified applied electric field is $-\alpha E^2/2$, rather than $-\alpha E^2$. In matter, the dipole moment per unit volume is the polarization density $\mathbf{P}$.

Free charge is charge assigned to externally supplied or mobile carriers in a macroscopic description. Bound charge describes the net charge associated with a material's polarization density $\mathbf{P}$. Its bulk and surface densities arewhere the normal points out of the polarized material. Uniform bulk polarization density has no bulk bound charge, but it can still have surface bound charge.

The electric field is sourced by the total electric charge. Introducing the electric displacement field separates the free source in the macroscopic field equation:This does not mean that bound charges are physically absent from $\mathbf{D}$: they are represented through $\mathbf{P}$. In a linear isotropic dielectric, $\mathbf{P}={ϵ}_0{\chi }_e\mathbf{E}$ and $\mathbf{D}=ϵ\mathbf{E}$, with $ϵ={ϵ}_0(1+{\chi }_e)$.

Across a stationary ordinary dielectric interface, electrostatics gives continuity of tangential electric field, while a free sheet charge givesThe normal electric field need not be continuous. For a fully filled parallel-plate capacitor at fixed free plate charge, polarization reduces the internal electric field by ${ϵ}_r$ and increases capacitance by the same factor. If a battery instead holds the voltage fixed, extra free plate charge flows from the battery; the constraint must be stated before comparing stored energies.^[ref]

A dielectric responds to an electric field mainly by displacing or orienting bound charges, rather than by sustaining a steady conduction current. The polarization density $\mathbf{P}$ is electric dipole moment per unit volume. It creates bound chargeSeparating these charges from free charge motivatesFor an isotropic linear dielectric, $\mathbf{P}={ϵ}_0{\chi }_e\mathbf{E}$, soThe electric susceptibility ${\chi }_e$ describes material polarization and is not the magnetic susceptibility. More generally it is a tensor and can depend on frequency, field strength and temperature.

Electronic polarization displaces an electron cloud relative to its nucleus; ionic polarization displaces positive and negative ions; orientational polarization partially aligns permanent molecular dipoles against thermal disorder. For independent permanent moments of magnitude $p$, weak-field orientational response gives ${\chi }_e\simeq n{p}^2/(3{ϵ}_0{k}_{B}T)$ when local-field corrections and interactions are negligible. This explains a common inverse-temperature contribution without asserting that every dielectric follows that law.

At a static interface, $\mathbf{n}\cdot ({\mathbf{D}}_2-{\mathbf{D}}_1)={\sigma }_f$ and the tangential electric field is continuous. Bound surface charge is already included through $\mathbf{P}$. For a homogeneous filled capacitor, $C=ϵA/d$, and a reversible linear dielectric stores energy density $u=\mathbf{E}\cdot \mathbf{D}/2$. At fixed voltage, insertion raises the stored field energy but the voltage source also supplies energy; force arguments must include that source. At fixed charge the capacitor energy instead decreases on insertion.

At frequencies too high for a polarization mechanism to follow the field, its contribution weakens. A complex permittivity represents dissipative dielectric loss as well as phase lag; the sign of its imaginary part depends on the time convention. Strong fields can cause nonlinear response or dielectric breakdown, beyond the reversible linear model.

An electrical insulator has no freely conducting bulk charge in the ideal static description, but an applied electric field can displace bound positive and negative charge relative to one another. The resulting electric dipole moments per unit volume define the polarization density $\mathbf{P}$. Distortion of electronic charge clouds, relative displacement of ions, and partial alignment of permanent molecular electric dipoles can all contribute. Thermal agitation opposes the last mechanism.

For a weak field in a linear isotropic dielectric, the constitutive law isHere ${\chi }_e$ is the electric susceptibility, $ϵ$ is the permittivity, and $\mathbf{D}$ is the electric displacement field. In an anisotropic material, ${\chi }_e$ is a tensor and $\mathbf{P}$ need not be parallel to $\mathbf{E}$. These response laws describe the macroscopic field, not necessarily the microscopic field acting on one molecule.

Spatial variation and surface termination of the polarization density give bound charge and bound current through the bound charge densitieswhere $\hat{\mathbf{n}}$ is outward from the material. Thus uniform polarization density has no bulk bound charge, but generally has opposite bound charges on opposing surfaces. Gauss's law can be rewritten asWith no free surface charge, the normal component of $\mathbf{D}$ is continuous across an interface; the tangential electric field is continuous in electrostatics.

For example, fill a parallel-plate capacitor of plate area $A$ and gap $d$ with a uniform dielectric, neglecting fringing. At fixed free plate charge $Q$, $D=Q/A$, soThe induced bound surface charges oppose the original field, reducing the electric field and potential difference at fixed $Q$. At fixed applied potential difference, the field remains $V/d$ and the battery instead supplies more free charge. The electric displacement field separates these free-charge and bound-charge roles.

Permittivity describes how an electric field and a material's electric polarization combine into the electric displacement field. In a static, local response with linearity and isotropy, and no electric polarization at zero electric field, the constitutive equation isHere ${ϵ}_0$ is vacuum permittivity, while ${ϵ}_r$ is the relative permittivity, a dimensionless quantity. The SI unit of permittivity is farad per metre, $F/m$: multiplying it by an electric field in $V/m$ gives an electric displacement field in $C/{\mathrm{m}}^2$. A larger positive permittivity lets the same parallel-plate capacitor hold more plate electric charge at the same electric potential difference.

The material contribution is electric polarization $\mathbf{P}$, the electric dipole moment per unit volume. The electric displacement field and electric susceptibility ${\chi }_e$ satisfySubstitution gives the first constitutive equation. The electric field here is the averaged, total field inside the material, not just the field of the external plate electric charges. The continuum approximation averages over many chemical atoms or molecules; locality means that the electric polarization at a position depends on the electric field there. Static equilibrium, fixed material conditions and sufficiently small electric fields are needed for this scalar proportionality. ^[ref].

For an ideal parallel-plate capacitor completely filled by a uniform dielectric, hold the free plate electric charge magnitude $Q$ fixed and neglect the fringing field of a capacitor. Writing $A$ for the plate area, Gauss's law gives $D=Q/A$. ThusThe electric dipoles point along the electric field. Their surface electric charges, described by polarization density, oppose the field from the free plate electric charges. For a hypothetical dielectric with ${ϵ}_r=4$, the internal electric field is one quarter of its vacuum value, while $P=3D/4$. At fixed electric potential difference instead, the internal electric field stays approximately $V/d$ and the plate electric charge grows fourfold. These are different experimental constraints. ^[ref].

Permittivity is a useful material summary, not a universal constant of the material under every condition. Temperature, frequency and electric field strength can change the response. In a linear anisotropic dielectric, permittivity is a tensor, $D_i={\sum }_j{ϵ}_{ij}{E}_j$, so the electric displacement field need not be parallel to the electric field. At nonzero frequency, delayed electric polarization requires complex permittivity and may produce dielectric loss. ^[ref].