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The Fermi energy is the highest occupied one-particle energy in the ground state of a noninteracting Fermi gas at zero temperature, measured here relative to the lowest one-particle energy. The Pauli exclusion principle allows only one fermion in each complete one-particle quantum state, including its spin, so adding more particles fills progressively higher energy eigenstates. A cold gas can therefore have substantial kinetic energy even when its temperature is zero. In the thermodynamic limit, with the same energy reference, $E_F=\mu (T=0)$ where $\mu$ is the chemical potential.^[ref]

For a uniform, three-dimensional gas of noninteracting electrons, with spin one-half, equal populations of the two spin states, no applied magnetic field, and nonrelativistic particles of mass $m=m_e$,Here $n$ is the total number density, $V$ the volume, $p_F$ the Fermi momentum, $\hslash =h/(2\pi )$ the reduced Planck constant, and $k_B$ the Boltzmann constant. The electron Fermi temperature $T_F$ expresses the same energy scale in kelvin; it is not the actual gas temperature. Strong degeneracy of a degenerate electron gas means $T\ll T_F$. The momentum formula counts states and survives changing the energy–momentum relation, whereas $E_F=p_F^2/(2m)$ requires $p_F\ll mc$.^[ref]

The reference matters: the displayed $E_F$ excludes rest energy and sets the zero at $p=0$. Including rest energy shifts both the one-particle energy and the zero-temperature chemical potential by $m{c}^2$, leaving occupations unchanged. More generally, adding a constant $C$ to every one-particle energy also adds $C$ to $\mu$; the Fermi-Dirac distribution depends only on their difference. In a finite quantum system the chemical potential at zero temperature can lie between the last occupied and first empty energy eigenstates; its equality with the filling edge is a continuum statement.

At positive temperature, $E_F$ remains the zero-temperature scale associated with the specified number density. The Fermi level $\mu (T)$ must instead satisfy the particle-number conditionwhere $g(E)$ is the extensive density of states, including both spin states. Smearing the Fermi-Dirac distribution while arbitrarily holding $\mu =E_F$ generally changes $N$. This distinction matters when interpreting electron heat capacity and any experiment that infers temperature from an occupation profile.^[ref]

Choose $n=10^{28}{\mathrm{m}}^{-3}$ for a uniform noninteracting electron model with two equally populated spin states. This is an original worked example, not a measured number density assigned to an actual material. Using $m_e\simeq 9.10938\times 10^{-31}\mathrm{kg}$, $\hslash \simeq 1.05457\times 10^{-34}\mathrm{J}\mathrm{s}$, and $k_B=1.380649\times 10^{-23}\mathrm{J}{\mathrm{K}}^{-1}$ givesThe conversion uses $1\mathrm{eV}=1.602176634\times 10^{-19}\mathrm{J}$: an electronvolt is an energy unit, while a joule is its SI counterpart. The dimensions provide a quick check: $n^{1/3}$ is inverse length, $\hslash n^{1/3}$ has units of momentum, $p_F^2/m$ has units of energy, and $E_F/k_B$ has units of temperature. The ratio $p_F/(m_{e}c)\simeq 0.002574$ verifies the nonrelativistic limit for this model, where $c$ is the speed of light.

Increasing this chosen number density eightfold doubles the Fermi momentum and quadruples the Fermi energy, giving approximately $6.7701\mathrm{eV}$. The exponent $2/3$ has a geometric origin: the number of occupied states grows as the cube of a momentum radius, but kinetic energy of nonrelativistic particles grows as its square. This makes Fermi energy a useful bridge between a count of particles and a mechanical energy scale.

The Fermi wavevector is the radius of the occupied sphere in wavevector coordinates for an isotropic Fermi gas. In the uniform two-component electron model, $k_F=(3{\pi }^{2}n{)}^{1/3}$ and $E_F={\hslash }^2{k}_F^2/(2m_e)$ for nonrelativistic particles. Its units are inverse length, whereas the Fermi momentum has units of momentum.

Take a nonrelativistic particle of constant mass $m$ with energy $E>0$, and choose the same zero of potential energy on both sides of a rectangular potential barrier:The equality of the exterior potential energies matters: it gives the same exterior wavenumber $k=\sqrt{2mE}/\hslash$ and makes $T=|t{|}^2$. Here $\hslash =h/(2\pi )$ is the reduced Planck constant. This model has a finite jump in potential energy, no delta potential, and no absorbing term.

For $0<E<V_0$, the time-independent Schrödinger equation gives the spatial wavefunctionThe full stationary state is $\Psi (x,t)=\psi (x)e^{-iEt/\hslash }$. We set the incident probability amplitude to one and impose no incoming wave from the right; this scattering wavefunction is not a normalizable wavefunction. The tunnelling decay constant $\kappa$ describes exponential decay, rather than an oscillatory wavenumber in the barrier. Both exponential functions are needed on the finite interval: the growing term is not excluded by a condition at infinity.

The wavefunction and its derivative are continuous at each face, giving four linear matching conditions:Their solution supplies the transmission amplitudeA short derivation is to use the two right-face equations to express $A{e}^{\kappa a}$ and $B{e}^{-\kappa a}$ in terms of $t$, then substitute into the left-face equations. Taking the squared modulus gives the rectangular barrier transmission probability.

The Maxwell-Boltzmann distribution describes the random velocities and speeds of particles in a classical ideal gas at thermal equilibrium. Individual particles keep changing velocity through collisions, while the equilibrium probability distribution stays fixed. For one species of particle mass $m$ at positive temperature $T$, the characteristic scale iswhere $k_B$ is the Boltzmann constant. A signed velocity component follows a normal distribution; the nonnegative magnitude follows the Maxwell speed distribution. Their peaks differ because a speed measurement groups together all directions of motion.

Use the gas rest frame, three spatial dimensions, and nonrelativistic particles, with $k_{B}T\ll m{c}^2$ where $c$ is the speed of light. Assume a dilute gas whose interactions between encounters can be neglected in the ideal gas approximation and whose translational motion is classical. A sufficient condition for negligible quantum exchange effects is $n{\lambda }^3\ll 1$, where $n$ is the number density and $\lambda$ the thermal de Broglie wavelength. Diluteness alone does not guarantee thermal equilibrium; the gas must have equilibrated. These are the assumptions behind the classical Maxwell-Boltzmann velocity distribution. ^{[ref] [ref]}

The connection to Maxwell–Boltzmann statistics is the Boltzmann factor for translational kinetic energy, $E_{\mathrm{kin}}=m|\mathbf{v}{|}^2/2$. Normalizing $e^{-E_{\mathrm{kin}}/(k_{B}T)}$ over velocity gives a probability density; an occupation factor $e^{(\mu -E)/(k_{B}T)}$ instead specifies a mean occupation, with chemical potential $\mu$. Their normalizations serve different purposes. ^[ref]

This connects microscopic motion to measurements: a gas thermometer uses the ideal gas law, collisions and the mean free path govern transport, and measurements of spectral lines use thermal Doppler broadening to infer temperature. Each probes a different aspect of the same thermal motion.

In 1860, James Clerk Maxwell presented the component and speed laws in Part I, Proposition IV of Illustrations of the Dynamical Theory of Gases, pp. 22–23. His argument combined independence of the three velocity components with isotropy, and he explicitly compared the component law with the normal distribution of observational errors. Independence is an assumption of that argument; perpendicular coordinate axes alone do not establish it. ^[ref]

Consider a nonrelativistic particle of mass $m$ undergoing an elastic collision with a stationary free target of mass $M=Am$, where $A\ge 1$. Assume the outgoing direction is uniformly distributed over solid angle in the center of mass frame; this assumption concerns the scattering angle distribution and need not hold for every target or energy. Let $\mu$ be the cosine of that frame's scattering angle. Transforming the outgoing velocity back to the laboratory givesThe uniform distribution of $\mu$ on $[-1,1]$ makes $x$ uniform on $[\alpha ,1]$. For $A>1$, integration yieldsFor equal masses, take the limit $\alpha \to 0$: $\xi =1$. The expected value of the fractional energy after a collision is instead $\mathbb{E}[x]=(1+\alpha )/2$. These are different averages: averaging a logarithm does not give the logarithm of an average.

For independent collisions with the same distribution, the logarithms of successive energy ratios add. ThusHere $E_{\mathrm{geom}}$ is the geometric-mean energy, and $n_{\log }$ is a characteristic collision count for reaching an energy scale $E_{\ast }$. It is not an exact first-passage expected value. Individual histories fluctuate, and neither the time between collisions nor absorption is specified by this model.

In an original chosen example, set $E_0=10^6\mathrm{eV}$ and $E_{\ast }=0.025\mathrm{eV}$. Approximate hydrogen by $A=1$ and carbon by $A=12$. ThenThese are illustrative model values, not measured collision counts from 1934. The energy scale marks where neglected thermal motion matters; the calculation does not assert continued cooling to zero energy.

In neutron detection by proton recoil, a neutron strikes a hydrogen atomic nucleus, namely a proton, and the moving proton produces detectable ionization. Paraffin wax provides many hydrogen targets. There are two distinct questions: how much kinetic energy can a collision transfer, and how often does it occur? Elastic collision kinematics answers the first. It does not determine a collision cross-section or a detector's efficiency.

For the following derivations the target is initially at rest in the laboratory but is free to recoil. Its mass is finite. In particular a proton must not be treated as an immovable target. All massive particles are nonrelativistic particles, their translational kinetic energies are $m{v}^2/2$, and the collision changes no internal state. Target binding and thermal motion are neglected relative to the incident kinetic energy. These assumptions suit an introductory description of fast-neutron elastic collisions; they do not cover every neutron capture or other nuclear reaction.

Treat the incident and outgoing neutrons as free nonrelativistic particles outside the specimen. Their wave vectors, de Broglie wavelengths, momenta and kinetic energies obeyHere $k_i=|{\mathbf{k}}_i|$, $k_f=|{\mathbf{k}}_f|$, $m_n$ is the neutron mass, and $\hslash =h/(2\pi )$ uses the Planck constant. Subtracting the outgoing projectile quantities from the incoming ones gives the momentum transfer and energy delivered to the specimen:Thus $\mathbf{Q}$ has units of inverse length, rather than momentum. A positive $\omega$ means the specimen gains energy; negative $\omega$ means it supplies energy to the neutron. If the angle between incident and outgoing propagation directions is $2\theta$, the law of cosines givesKnowing the detector angle alone therefore leaves $Q$ undetermined unless the outgoing energy is known or an elastic scattering assumption is justified.

For a reproducible unit conversion choose $m_n=1.67492750056\times 10^{-27}\mathrm{kg}$, $h=6.62607015\times 10^{-34}\mathrm{J}\mathrm{s}$ and $1\mathrm{eV}=1.602176634\times 10^{-19}\mathrm{J}$. The first is a recommended central value; the latter two conversions are exact.^[ref] With $1$ ångström equal to $10^{-10}\mathrm{m}$ and $1\mathrm{meV}=10^{-3}$ electronvolts, substitution into $E=h^2/(2m_n{\lambda }^2)$ givesSquare brackets here mean the numerical value in the indicated unit. For an original chosen example, ${\lambda }_i=2$ ångströms and ${\lambda }_f=2.5$ ångströms give $E_i\simeq 20.451\mathrm{meV}$, $E_f\simeq 13.089\mathrm{meV}$ and $\hslash \omega \simeq 7.362\mathrm{meV}$. At $2\theta =60^{\circ }$, $Q\simeq 2.879{\mathring{\mathrm{A}}}^{-1}$. These values stipulate an allowed projectile geometry; they do not assert that any particular specimen has an excitation there.

Integrating Maxwell–Boltzmann statistics over momentum for nonrelativistic particles of mass $m$, spin-state count $g_s$, and energy $m{c}^2+p^2/(2m)$ gives

For fixed $0<E<V_0$ and $\kappa a\gg 1$, the exact rectangular barrier transmission probability givesThis is the leading term of an asymptotic expansion: the wavefunction amplitude scale is $e^{-\kappa a}$, and the transmission probability scale is $e^{-2\kappa a}$, with an interface prefactor. Increasing width by $\Delta a$ multiplies this approximation by $e^{-2\kappa \Delta a}$. At fixed incident energy, increasing barrier height increases the tunnelling decay constant as $\sqrt{V_0-E}$; heavier nonrelativistic particles also have stronger suppression. For the numerical example in rectangular barrier transmission probability, the approximation gives $0.01397$, compared with the exact $0.01388$.

The regime condition matters. Near $E=V_0$ at fixed width, $\kappa a$ tends to zero and the opaque barrier approximation fails; use the exact threshold value. For $\kappa a\ll 1$, expansion of the hyperbolic sine givesThis tends to one as $a\to 0$ at fixed $E,V_0$, but the condition $\kappa a\ll 1$ alone does not imply nearly perfect transmission if the remaining factor is large. At $E>V_0$, use the oscillatory formula and its scattering resonances, rather than an exponential decay law.

Use natural units $\hslash =c=k_B=1$ and the unreduced Planck mass $M_P=G^{-1/2}$. Neutrino decoupling occurs when the weak interaction rate falls below the Hubble parameter. The weak-decoupling temperature estimate equates the given rate with the radiation-era expansion rate:Here $g_{\ast }$ counts the effective number of relativistic energy degrees of freedom, and the Fermi constant is $G_F\simeq 10^{-5}{\mathrm{GeV}}^{-2}$. The omitted reaction-rate coefficients make this an order-of-magnitude estimate: decoupling occurs at a temperature of order one MeV.

The charge-conserving channel is $n+{\nu }_e\leftrightarrow p+e^{-}$, together with $p+{\bar{\nu }}_e\leftrightarrow n+e^{+}$. The positron sign in the printed neutron-capture channel violates electric charge conservation. Chemical equilibrium requires ${\mu }_n+{\mu }_{{\nu }_e}={\mu }_p+{\mu }_e$. Negligible lepton chemical potentials therefore give ${\mu }_n\simeq {\mu }_p$. Since neutrons and protons are nonrelativistic particles, their Maxwell-Boltzmann distribution givesBoth nucleons have two spin states, and their masses agree closely in the prefactor. Thus neutron-proton chemical equilibrium impliesThe heavier neutron is suppressed by a Boltzmann factor.

For the deuterium equilibrium abundance, retain the paper's convention $B=m_D-m_n-m_p<0$; the positive nuclear binding energy is ${\epsilon }_D=-B\simeq 2.22\mathrm{MeV}$. Chemical equilibrium of $n+p\leftrightarrow D+\gamma$ gives ${\mu }_D={\mu }_n+{\mu }_p$ because the equilibrium photon chemical potential vanishes. Using the nonrelativistic Maxwell--Boltzmann number density for each species and dividing givesHere $g_D=3$ and $g_n=g_p=2$. With the baryon-to-photon ratio $\eta =n_B/n_{\gamma }$, the photon number density $n_{\gamma }=2\zeta (3)T^3/{\pi }^2$, and $m_D\simeq 2m_N$, $m_n\simeq m_p\simeq m_N$, this becomesIn this convention $X_D=n_D/n_B$ counts nuclei, so its contribution to the fraction of baryons in deuterium is $2X_D$.

The deuterium bottleneck explains why helium-4 formation waits until $T$ is far below ${\epsilon }_D$. At higher temperature, there are vastly more photons than baryons; even the dilute energetic tail can destroy newly formed deuterium. A crude estimate balances ${\eta }^{-1}{e}^{-{\epsilon }_D/T}$ against one, giving $T\sim {\epsilon }_D/\log ({\eta }^{-1})\sim 0.1\mathrm{MeV}$ for $\eta$ of order $10^{-9}$. The power-law factors in the deuterium equilibrium abundance and the nuclear reaction rates refine this estimate. Once stable deuterium accumulates, further reactions can efficiently place nearly all surviving neutrons into helium-4.

Write $r_N=n_n/n_p$ at the onset of nuclear burning. Each helium-4 nucleus requires two neutrons and contains four baryons. Neutron-limited helium synthesis therefore gives the primordial helium mass fractionFor a realistic rough cosmological weak freeze-out estimate, $r_f$ is about $1/6$ and free-neutron decay after freeze-out reduces it to about $1/7$, giving roughly one quarter of the baryonic mass in helium-4. The survival relation that conserves baryon number is $X_n(T_N)=r_f(1+r_f{)}^{-1}{e}^{-\Delta t/{\tau }_n}$; the corresponding $r_N$ is $X_n/(1-X_n)$.

The rough neutrino decoupling rate by itself does not determine that one-quarter value. Substituting $T_d=1.8\mathrm{MeV}$ literally into $e^{-Q/T_d}$ would give $r\simeq 0.49$ and $Y_4\simeq 0.65$ before neutron decay. Neutron-proton chemical equilibrium persists to a lower temperature, approximately $0.7$--$0.8\mathrm{MeV}$ once the actual conversion rates are included. The rate scaling fixes the MeV scale; accurate abundances need the conversion coefficients and the delay through the deuterium bottleneck. This sequence is described in David Tong's discussion of nucleosynthesis.

Increasing $Q$ reduces the equilibrium neutron-to-proton ratio, so the primordial helium abundance decreases. Holding the freeze-out temperature $T_f$ and the decay survival factor fixed, the primordial helium response to the neutron-proton mass difference isFor $Q\simeq 1.29\mathrm{MeV}$ and $T_f=0.7$--$0.8\mathrm{MeV}$ this is about $0.85$--$0.87$, a reduction of roughly fifteen percent. A larger $Q$ also changes neutron decay and detailed weak rates; their quantitative effects require more microscopic information. The sign from the Boltzmann factor is already clear.

For a nonrelativistic particle, $E(p)=m{c}^2+p^2/(2m)$. The Gaussian integral yieldsIndeed ${\int }_0^{\infty }{p}^2{e}^{-p^2/(2m{k}_{B}T)}dp=\sqrt{\pi }(2m{k}_{B}T{)}^{3/2}/4$, which combines with $4\pi /h^3$ to give the prefactor. For the two species this givesChemical equilibrium imposes ${\mu }_a+{\mu }_{\alpha }={\mu }_b+{\mu }_{\beta }$. If the two massless bath species have zero chemical potentials, then ${\mu }_a={\mu }_b$; their masses alone do not imply this chemical-potential condition.

Weak reactions such as $n+{\nu }_e\leftrightarrow p+e^{-}$, with leptons treated as relativistic, interconvert neutrons and protons. Negligible lepton chemical potentials give approximately $n_n/n_p=\exp [-(m_n-m_p)c^2/(k_{B}T)]$, since their degeneracies and masses are nearly equal. Equilibrium favors protons increasingly as temperature falls. But the weak reaction rate decreases faster than the expansion rate and eventually falls below it: cosmological weak freeze-out prevents the ratio from following its equilibrium exponential to zero. Free neutrons subsequently decay, reducing the frozen ratio further.

In Big Bang nucleosynthesis, cooling eventually makes deuterium survive photodissociation. Nuclear reactions then build helium through deuterium and the light intermediate nuclei, locking almost all surviving neutrons into stable helium-four. Neglecting binding-energy corrections and taking $r=n_n/n_p\le 1$, each helium nucleus uses two neutrons and two protons, so $n_{\mathrm{He}}=n_n/2$ andFor example $r=1/7$ gives a helium mass fraction $1/4$, with the remaining baryons predominantly hydrogen.

For injected velocity $\mathbf{v}=v\hat{\mathbf{x}}$, the Lorentz force isFor nonzero electric charge and nonzero operating current, the velocity selector condition isThe requested nonrelativistic kinetic energy is consequentlyBoth electric current and electric charge cancel. Reversing the sign of $q$ reverses both component forces and preserves their cancellation. The dimensions are consistent because $R/{\mu }_0$ has units of speed, while $w/d$ is dimensionless. The assumed nonrelativistic particle regime requires $Rw/({\mu }_{0}d)\ll c$; the problem supplies no values with which to evaluate a numerical energy.

A freely falling particle's physical momentum is measured in the local orthonormal frame of a comoving observer. With proper peculiar velocity $\mathbf{v}=ad\mathbf{x}/dt$ and Lorentz factor $\gamma =(1-v^2{)}^{-1/2}$, it is $m\gamma \mathbf{v}$. It differs by one factor of the scale factor from the conserved comoving momentum. For a nonrelativistic particle, its peculiar velocity therefore decays as $a^{-1}$.

The coefficient $A$ has dimensions of electric current density divided by squared temperature. For ideal nonrelativistic particles with the free electron mass, two spin states, a planar uniform surface, and unit escape transmission, the thermionic tail-flux derivation giveswhere $e$ is the positive elementary charge and $h$ is the Planck constant. The two area units differ by a factor of $10^4$. A fitted $A$ need not equal $A_0$: reflection at the surface, the electronic band structure, and uncertain emitting area affect the inferred coefficient. A constant escape transmission $\tau$ would give $A=\tau A_0$ in this simple model; an energy-dependent transmission generally requires an integral instead.

The name joins Owen Willans Richardson with Saul Dushman. Dushman's 1923 paper develops a thermodynamic treatment of electron emission analogous to evaporation and evaluates the prefactor using quantum ideas.^[ref]

For the uniform noninteracting electron model with two spin states and kinetic energy of nonrelativistic particles $E=p^2/(2m_e)$, count all available one-particle states up to an energy $E\ge 0$:This extensive density of states has units of inverse energy; $g(E)/V$ is the density of states per unit volume. Availability and occupation are different: $g(E)$ is positive above $E_F$, but at zero temperature those states are empty. The occupied energy distribution is $g(E)f(E)$, with the Fermi-Dirac distribution reduced to $f(E)=1$ below $E_F$ and $f(E)=0$ above it. The convention at the exact boundary does not affect a continuum integral.

With the dimensionless quantity $x=E/E_F$, the occupied count per $dx$, divided by the total particle number, is $3\sqrt{x}/2$ for $0<x<1$. Its area is one. Weighting this by $E$ gives the internal energy and its mean per particle:Thus the highest occupied energy and the mean energy differ. For the Fermi energy of a model electron gas, $U/N\simeq 1.0155\mathrm{eV}$. At fixed $N$, $E_F\propto V^{-2/3}$, so the derivative $P=-(\partial U/\partial V{)}_N$ gives the electron degeneracy pressure $P=2n{E}_F/5$. The same state-counting geometry therefore predicts a nonzero pressure at zero temperature.

A single recoil endpoint leaves a tradeoff between incident speed and projectile mass. Two targets can remove the unknown incident speed. Assume both runs sample the same maximum projectile speed $v$ and that single elastic collisions reach the endpoint. For initially stationary target masses $M_1<M_2$, let their maximum recoil speeds be $u_1,u_2$. The maximum elastic recoil energy fraction calculation givesIf energies rather than speeds are inferred, use $R=\sqrt{T_{1,\max }{M}_2/(T_{2,\max }{M}_1)}$. The energy ratio itself is not the speed ratio.

For the stipulated $4\mathrm{MeV}$ example, hydrogen and nitrogen giveThe inferred mass then determines $v=u_1(m+M_1)/(2m)$. Changing the assumed mass to improve one recoil endpoint changes the prediction for the other: this is the constraining power of the comparison.

James Chadwick's June paper instead used approximate endpoints $u_p=3.3\times 10^{7}m/s$ and $u_N=4.7\times 10^{6}m/s$, obtaining $m/m_p\simeq 1.15$; it allowed roughly ten percent uncertainty in $u_N$. This was a rough mass comparison.^[ref]

The inverse calculation has useful built-in checks. A positive finite mass requires $1<R<M_2/M_1$. As $R$ approaches $1$, distinguishing large projectile masses becomes difficult. Differentiation givesUncertain recoil endpoints therefore produce an uncertain inferred mass; the collision model cannot turn imprecise range measurements into exact spectroscopy. If different target runs select different incident energy groups, the common-$v$ cancellation also fails.

For comparison, Compton scattering of a photon of energy $E_{\gamma }$ from a stationary free target of mass $M$ has the exact relativistic endpointThis follows by combining momentum conservation with the target's relativistic energy, maximizing transfer when the photon reverses direction. Unlike the massive-projectile calculation, this equation does not approximate the incident photon as a nonrelativistic particle.

As a separate, explicitly hypothetical test, take $m_p{c}^2=938\mathrm{MeV}$ and target rest energies $938\mathrm{MeV}$ and $14\times 938\mathrm{MeV}$. To reproduce the stipulated hydrogen recoil endpoint $T=4\mathrm{MeV}$, the photon would need $E_{\gamma }\simeq 45.36\mathrm{MeV}$. The same photon would give the heavier target at most $0.311\mathrm{MeV}$, whereas the stipulated massive projectile gave $0.996\mathrm{MeV}$. This is the structure of a two-target discrimination, not a transcription of a 1932 measurement. Actual radiation can contain more than one energy group or both photons and neutrons; a useful model must account for the observed endpoints and their origin together.