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Let starred quantities denote the capacitor's rest inertial frame, $u_0={ϵ}_0{E}^2/2$, $\beta =v/c$, and $\gamma =(1-{\beta }^2{)}^{-1/2}$. Work in the uniform interplate region of an ideal parallel-plate capacitor, neglecting its fringing field of a capacitor. To transform from that rest inertial frame to a laboratory in which the capacitor moves along $+x$, use the positive-sign Lorentz transformationFor a purely electric field, the spatial block of the electromagnetic stress-energy tensor isThis is the negative of the Maxwell stress tensor: it has $-u_0$ along the electric field and $+u_0$ perpendicular to it. The stress contribution to energy transport in a moving capacitor is essential to the Lorentz transformation of the energy density and flux.

Plates parallel to $xy$. Choose ${\mathbf{E}}_{\ast }=E\hat{\mathbf{z}}$ and ${\mathbf{B}}_{\ast }=0$. The electromagnetic field tensor and electromagnetic stress-energy tensor areThe transformed nonzero independent electromagnetic field tensor components are $F^{03}=\gamma E/c$ and $F^{13}=\gamma \beta E/c$. Thus $\mathbf{E}=\gamma E\hat{\mathbf{z}}$ and $\mathbf{B}=-\gamma vE\hat{\mathbf{y}}/c^2$, consistent with $\mathbf{B}=\mathbf{v}\times \mathbf{E}/c^2$. Transforming the electromagnetic stress-energy tensor givesIn particular, the laboratory Poynting vector is $\mathbf{S}=2u_0{\gamma }^{2}v\hat{\mathbf{x}}$, and the electromagnetic energy density is $u=u_0{\gamma }^2(1+{\beta }^2)$. The ratio $S_x/u=2v/(1+{\beta }^2)$ is subluminal for $v<c$, but differs from the capacitor's velocity. The difference from a simple convective flux isThe extra term is $v{T}_{\ast }^{xx}$, the rest-frame stress multiplied by the velocity. This shows why treating stored field energy as an unstressed parcel moving rigidly with the plates misses part of the energy transport.

Plates parallel to $yz$. Now ${\mathbf{E}}_{\ast }=E\hat{\mathbf{x}}$. The rest tensors areThe electric field is parallel to the Lorentz boost, so $F^{01}=E/c$ remains unchanged and $\mathbf{B}=0$. The cancellation between $T_{\ast }^{00}$ and $T_{\ast }^{11}$ givesThere is no Poynting flux in the ideal interior in this orientation, although the region containing the electric field moves. The longitudinal negative stress contribution cancels the convective term: $S_x={\gamma }^{2}v(u_0+T_{\ast }^{xx})=0$. Field energy is removed at the receding boundary and supplied at the advancing boundary by work on the charged plates; it need not flow through the interior to accompany the moving region. At edges, omitted fringing fields provide additional local structure.

For a finite idealized interplate rest volume $V_0$, length contraction gives $V=V_0/\gamma$. The field-only integrated laboratory energies would consequently be $U_{xy}=\gamma (1+{\beta }^2)U_0$ and $U_{yz}=U_0/\gamma$, with $U_0=u_0{V}_0$. Their different transformation laws are not paradoxical: the field alone is not a closed system. Include the plates and the supports holding them apart, whose mechanical stresses balance the Maxwell stress tensor. The total closed-system four-momentum then has the ordinary Lorentz transformation law. This is the same distinction between a subsystem and a conserved whole that appears in b.

Let $s=k^{\mu }{x}_{\mu }$. The Lorenz gauge condition on the plane electromagnetic wave givesThe vacuum wave equation gives $k_{\mu }{k}^{\mu }=0$ for a nonzero amplitude; equivalently $k^0=\omega /c$ and $|\mathbf{k}|=\omega /c$. Use the gauge transformation $A^{\prime \mu }=A^{\mu }+{\partial }^{\mu }\chi$ withBecause $\square \chi =0$, this is a residual Lorenz gauge symmetry and $k_{\mu }{ϵ}^{\prime \mu }=0$. For a propagating plane electromagnetic wave, $k^0\ne 0$, so take $\lambda =-{ϵ}^0/k^0$. ThenThe second equality follows from $-k^0{ϵ}^{\prime 0}+\mathbf{k}\cdot {\mathbf{ϵ}}^{\prime }=0$. The electric field and magnetic field are unchanged by this gauge transformation. Thus Lorenz gauge permits a representative in radiation gauge; Lorenz gauge alone does not require the spatial amplitude of every representative to be transverse.

Choose Minkowski metric $(+,-,-,-)$, so $A_{\mu }=(\varphi /c,-\mathbf{A})$ and $d\tau =dt\sqrt{1-v^2/c^2}$. In laboratory time the relativistic charged-particle action has LagrangianHere $e$ denotes the signed particle charge in the action. The canonical momentum and the position derivative areThe Euler-Lagrange equation therefore givesThe last term is $(\mathbf{v}\times \mathbf{B}{)}_i$, and the first two terms form the electric field. Thus the relativistic Lorentz force equation isIts power relation and acceleration form areThe power relation follows by taking the scalar product with $\mathbf{v}$ and using the relativistic energy-momentum relation. It also shows why the magnetic field alone cannot change the particle's energy.

For a uniform constant electric field and zero magnetic field, the mechanical momentum changes linearly even though the velocity does not:Invert $\mathbf{p}=m\gamma \mathbf{v}$ using $\gamma =\sqrt{1+p^2/(m^2{c}^2)}$. The result for arbitrary initial direction isEquivalently, $\mathbf{v}=c\mathbf{p}/\sqrt{m^2{c}^2+p^2}$. This gives $\mathbf{v}(0)={\mathbf{v}}_0$ and guarantees $|\mathbf{v}|<c$ at every finite momentum. The transverse momentum stays constant, but its velocity component generally decreases because the Lorentz factor increases. Thus an initial transverse velocity must not be treated as constant during the electric acceleration; this is the relativistic motion in a constant electric field with transverse momentum effect.

With no electric field, the power relation from part (a) givesConsequentlyThe magnetic part of the relativistic Lorentz force changes the direction of mechanical momentum, but performs no work. This conclusion does not require the magnetic field to be spatially uniform: it follows from the local orthogonality of $\mathbf{v}$ and $\mathbf{v}\times \mathbf{B}$.

A constant electrostatic energy offset is removed locally by the quantum phase substitution $\psi =e^{-i{V}_{0}t/\hslash }{\psi }_0$, since $(i\hslash {\partial }_t-V_0)\psi =e^{-i{V}_{0}t/\hslash }i\hslash {\partial }_t{\psi }_0$. Therefore the two frequency branches becomeThe normalization uses the kinetic frequency ${\omega }_k$, while the canonical energy eigenvalues are $E=V_0\pm \hslash {\omega }_k$. The opposite-frequency branch is not obtained by replacing ${\omega }_k$ by the same shifted positive frequency in both terms. A globally constant offset produces no electric field, whereas different offsets on opposite sides of a step cannot be removed by a single smooth global phase.

Work in temporal gauge, with zero scalar potential, and use the charge sign exactly as in the given covariant spatial derivative. A spatially uniform vector potential acts on a Fourier mode asThere are no spatial derivatives of $\mathbf{A}$. Substitution into the field equation and multiplication by $c^2$ therefore givesThe canonical wavevector $\mathbf{k}$ is conserved by spatial translation symmetry; the kinetic momentum is $\hslash \mathbf{k}-e\mathbf{A}(t)$. The absence of a term involving $\dot{\mathbf{A}}$ in this mode equation follows from temporal gauge and the spatial minimal-coupling operator. The electric field still affects evolution through the changing oscillator frequency.

The Paul trap alternates focusing and defocusing electric forces. Their time average along a moving trajectory need not vanish, even when the electric field averages to zero at every fixed point. A spatial gradient makes the fast displacement correlate with the driving electric field; the RF-averaged trapping potential calculates the resulting restoring force.

Wolfgang Paul's lecture describes hyperbolic ring/endcap electrodes, loading by electron-impact ionization of low-pressure gas, and resonant ejection through an endcap hole into an electron multiplier. Sweeping RF voltage produces an air mass spectrum.^[ref]

At the surface of a perfect conductor, the tangential electric field and normal magnetic field vanish. An incident plane electromagnetic wave is therefore accompanied by a reflected wave whose tangential electric field cancels the incident field at the surface.

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].

The permittivity tensor is the linear material-response matrix relating electric displacement field to electric field at a specified frequency. An isotropic local medium has ${ϵ}_{ij}=ϵ{\delta }_{ij}$. A magnetically biased transparent medium can have an imaginary antisymmetric transverse contribution; its eigenmodes can have opposite circular polarizations and different refractive indices.

Phase conjugation creates a returning monochromatic wave whose spatial complex amplitude is proportional to the complex conjugate of the incident field. Fix the time convention throughout:Here $E$ is one scalar component of the electric field, $A\ge 0$ is the wave amplitude, $\omega >0$ is the angular frequency, and $\gamma$ is a spatially constant complex number setting the return strength and reference wave phase. The complex conjugation acts on $U$, including its spatial carrier, while the time factor remains $e^{-i\omega t}$. Conjugating both factors would merely give another representation of the same real field. With $\gamma =1$, the new real field equals $E(\mathbf{r},-t)$ in this ideal monochromatic wave model; that identity does not assert reversal of an arbitrary pulse or of the apparatus producing it.

The spatial wave phase becomes $-\varphi +\arg \gamma$, so the local wavevector changes from $\nabla \varphi$ to $-\nabla \varphi$. For example, $U=A{e}^{i(k_{x}x+k_{z}z)}$ with $k_z>0$ becomes $\gamma A{e}^{-i(k_{x}x+k_{z}z)}$: both components of the wavevector reverse. In a transparent stationary medium with isotropy and positive refractive index, light rays follow the wavevector, giving counterpropagation. The same wavefronts now have opposite propagation normals. This is why phase conjugation can return a distorted beam toward its origin: it reverses the detailed spatial wave phase, rather than requiring that wave phase to be flat.

The attractive application is correction of optical aberrations accumulated on an outward trip. The return uses the distortion itself as the prescription for correction, as the original thin phase-plate cancellation by phase conjugation example makes explicit. An experimentally accessible implementation measures the spatial wave phase and uses a spatial light modulator to generate its negative; digital optical phase conjugation describes an inspected 2010 demonstration of recovery through multiple scattering.

Phase matching makes wave amplitudes emitted at different depths add coherently. Consider collinear plane waves in a uniform transparent material of length $L$, with fixed polarization of waves and nonzero selected nonlinear optical susceptibility. Assume negligible pump depletion, negligible absorption, an initially absent harmonic, and a wide beam for which diffraction is negligible. The pump's wave amplitude is then constant throughout the interaction.

The pump electric field has spatial wave phase $k_{\omega }z$; its quadratic source has spatial wave phase $2k_{\omega }z$. The freely propagating harmonic has wave number $k_{2\omega }$. Define the second-harmonic phase mismatch byFor the chosen complex-field convention, the outgoing harmonic wave amplitude, up to an overall constant and propagation phase, is proportional toChoosing the conjugate complex-field convention reverses the exponent's sign without changing the wave intensity. Taking the squared complex modulus givesHere $C$ is fixed for the chosen modes and material; its dimensions accommodate the stated wave intensity convention. The quadratic pump dependence follows because the source wave amplitude is proportional to $E_0^2$, whereas $I_{\omega }$ is proportional to $E_0^2$. The sinc function comes from summing contributions along the whole material, just as a finite aperture produces diffraction through addition of complex amplitudes.

At $\Delta k=0$, the integral is $L$ and the harmonic wave intensity grows as $L^2$. At $\Delta kL=2\pi$, all those contributions cancel. This cancellation needs no absorption: their wave phases wind through a full turn. At high conversion, the constant-pump assumption fails, so the $L^2$ law cannot continue indefinitely. Tight focusing, finite optical pulses, absorption, and transverse separation of modes also require a more complete model.

Optical dispersion generally makes $n_{2\omega }\ne n_{\omega }$. In a suitable crystal, birefringence allows modes with different polarization of waves to experience different refractive indices, making their selected values equal. The appropriate crystal direction and allowed nonlinear optical susceptibility component must both work.^[ref]

For a worked calculation, choose $L_0=1\mathrm{mm}$ and $\Delta k=\pi \mathrm{m}{\mathrm{m}}^{-1}$. At $L=L_0$, the harmonic wave intensity is $4/{\pi }^2\simeq 0.4053$ of its perfectly matched value. At $L=2L_0$ it vanishes in this model. More material can therefore reduce the output. If instead $\Delta k=0$, doubling $L$ multiplies output by four. The two curves retain that common normalization, so their different peak heights are meaningful.

For the overlapping monochromatic wave components, let $d$ be the thickness and ${\lambda }_0$ the vacuum wavelength. Define $\Delta n=n_s-n_f>0$ using the slow and fast refractive indices. With complex amplitude convention $e^{i(kz-\omega t)}$, the accumulated slow-minus-fast phase difference isThis is the optical path difference $\Delta nd$ expressed as a wave phase. It is a signed accumulation convention; with the opposite time convention the sign reverses. The outgoing polarization of an electromagnetic wave depends on $\delta$ modulo $2\pi$. Here the positive slow-minus-fast $\Delta n$ differs from the signed principal-index $n_e-n_o$ used in the parent birefringence entry when $n_e<n_o$.

For an original worked example, stipulate $\Delta n=0.0100$ at ${\lambda }_0=600\mathrm{nm}$ and a uniform thickness $d=15.0\mu \mathrm{m}$. These are design assumptions, not measured material data. The optical path difference is $150\mathrm{nm}$, soIt is a quarter-wave plate. At the same wavelength and refractive indices, doubling $d$ to $30.0\mu \mathrm{m}$ gives $\delta =\pi$, a half-wave plate. A $1.0\mu \mathrm{m}$ thickness increase changes $\delta$ by $\pi /30$, or $6^{\circ }$; retaining the same birefringence at $500\mathrm{nm}$ would instead give $\delta =3\pi /5$ for the $15.0\mu \mathrm{m}$ plate. Real refractive indices also vary with wavelength, so this last calculation explicitly neglects optical dispersion.

For these equal transmitted wave amplitudes, orthogonal projection onto a polarizer crossed with the initial $45^{\circ }$ linear polarization gives a simple independent readout. After removing a common wave phase, the component complex amplitudes are proportional to $(1,e^{i\delta })/\sqrt{2}$; orthogonal projection onto $(1,-1)/\sqrt{2}$ gives $(1-e^{i\delta })/2$. Squaring its modulus yields $I_{\perp }/I_{\mathrm{in}}={\sin }^2(\delta /2)$: zero at $d=0$, one half at $15\mu \mathrm{m}$, and one at $30\mu \mathrm{m}$. This assumes ideal polarizers, negligible specular reflection and wave absorption, overlapping components and stable relative wave phase. It measures a periodic function of phase retardation, so one brightness measurement cannot determine the thickness uniquely.

In the published chlorine experiment, negative ions were accelerated and mass-selected, then overlapped with a tunable laser beam. A downstream electric field deflected charged ions; neutral chemical atoms continued to a plate, whose secondary electrons were counted. Scanning the laser frequency produced an onset in this neutral-atom signal. The apparatus therefore inferred an electron affinity from a threshold, rather than measuring the heat of attachment.^[ref]

Reversing the laser direction and averaging the two thresholds corrected the first-order Doppler shift. A Fabry–Pérot interferometer and reference spectral lines calibrated the frequency. Finite laser bandwidth, unresolved quantum state splitting and shifts of the calibration lines limited the inference; the authors included these effects in fitting and the error estimate. The level diagram shows only the extracted gap, not a measured signal curve.^[ref]

A photodiode is a semiconductor diode producing photocurrent from photon absorption. Exciting an electron across the band gap leaves an electron hole. The depletion region's electric field separates the charge carriers; others can arrive by diffusion before electron-hole recombination. Contacts complete the electrical circuit.^[ref]

The useful bridge is from light to a measurable electric current: spectral responsivity converts incident radiant flux into photocurrent, while quantum efficiency counts collected signal charge carriers per incident photon. These answer different questions: how much electric current one watt produces, and how many incident photons contribute to the signal. The worked calculation below makes their relationship explicit.

The photoelectric effect is the release of electrons from matter following photon absorption. Here the focus is emission from a metal surface into vacuum: a photon supplies energy, the work function pays the escape cost, and the remainder can become the emitted electron's kinetic energy. A photocurrent counts collected electric charge; a stopping potential probes the upper kinetic energy limit. These are different measurements.

In 1905, Albert Einstein proposed that an individual light quantum could transfer its whole energy to one electron. His §8 allowed losses before escape, distinguished the fastest emitted electrons from the rest, and predicted a straight stopping potential versus frequency relation with a material-independent slope. He separately predicted that changing light intensity changes the number emitted without changing their velocity distribution under otherwise identical conditions. He also discussed incomplete transfer and limits to the account.^[ref]

The useful modern starting model is a clean, homogeneous metal with independent single-photon events, negligible initial thermal broadening, negligible lowering of the surface barrier by an applied electric field, and negligible electric fields from the emitted electrons themselves. Specify the surface and its work function; it is not enough to name the bulk material. The Einstein photoelectric equation describes the upper edge of the emission energy distribution. It neither predicts that every absorbed photon liberates an electron nor supplies the whole photocurrent curve. Its appeal is that a complicated surface process still exposes the universal Planck constant through a simple slope.

The photoelectric saturation current is the photocurrent reached when increasing the collecting electric potential difference no longer increases the fraction of available emitted electrons collected. It is saturation with collecting voltage at fixed illumination. It does not mean that increasing incident light intensity cannot increase emission.

If $P$ is incident radiant flux on the emitting area and $\eta$ is the external quantum efficiency for producing escaping electrons, then the incident photon arrival rate is $P/(h\nu )$ and complete collection gives $I_{\mathrm{sat}}=e\eta P/(h\nu )$. For the example's $\nu =8.00\times 10^{14}\mathrm{Hz}$, choose $\eta =0.10$ and $P=1.00\mu \mathrm{W}$. The calculated photon arrival rate is $1.886488\times 10^{12}{\mathrm{s}}^{-1}$ and $I_{\mathrm{sat}}=30.224866\mathrm{nA}$. Doubling $P$ doubles this current to $60.449731\mathrm{nA}$ while leaving $V_s$ fixed. At fixed illuminated area this doubles the irradiance. Changing frequency at fixed $P$ changes the arrival rate as well as the photon energy; $\eta$ can also change, so there is no general rule that a higher frequency gives a larger photocurrent.

A missing plateau can indicate incomplete collection or an electric field altered by the emitted electric charge. Heating, surface changes and additional emission channels can invalidate a constant $\eta$. Even a small amount of unwanted higher-frequency radiation can move an apparent endpoint. A stopping potential inferred from zero net current additionally needs background subtraction and a check for emission from the collector itself.

Photofragment-ion imaging detects fragment velocities by ionizing neutral products and mapping their motion onto a position-sensitive detector using an electric field. In a velocity-mapping implementation, the image radius measures transverse speed under fixed lens settings. Selecting an arrival-time slice helps extract the central plane of the three-dimensional distribution. Species identification and electronic quantum state selection are essential for turning a radius into a particular dissociation threshold.

This electric potential is harmonic and independent of $z$. Its electric field is linear in transverse position, with a saddle at the origin. For $A>0$, field lines approach along the $x$ axis and leave along the $y$ axis; off-axis field lines satisfy $xy=\mathrm{constant}$. Equipotentials satisfy $x^2-y^2=\mathrm{constant}$. This is a local planar electric quadrupole geometry, not the decaying far field of an isolated three-dimensional quadrupole.