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The Born rule connects a quantum state to measurement probabilities. Let $\{|j⟩\}$ be a complete orthonormal basis, finite or countably infinite, for a Hilbert space, and letAn ideal measurement distinguishing these basis vectors returns label $j$ with probabilityThis assignment is a physical measurement rule. Its compatibility with total probability one follows from orthonormality and normalization:The probabilities are the squared moduli, not the amplitudes themselves or the squares $a_j^2$. ^[ref].

If the basis is an eigenbasis of an observable, the reported numerical value is its eigenvalue. Several vectors can share one eigenvalue; the probability of that value is then the sum over the corresponding basis labels. More generally, a projective measurement with orthogonal projections $P_r$ assignsfor a pure state and a general density matrix $\rho$, respectively. This also covers mixed states and degenerate eigenspaces. The Born rule determines outcome statistics; the ideal conditional state change is specified separately by the Lüders rule. See projective measurement for that formulation and its assumptions. ^[ref].

For a worked example, take the normalized qubit quantum stateThe squared moduli add to $3/4+1/4=1$. A computational-basis measurement, equivalently a measurement of the $Z$ Pauli matrix, hasThese probabilities do not depend on the relative quantum phase $\varphi$. Now choose the Hadamard basiswhose vectors are eigenstates of the $X$ Pauli matrix, also used by the Pauli X gate. The new probability amplitudes and probabilities areBoth probabilities are nonnegative and their sum is one. The relative quantum phase becomes visible because the two probability amplitudes add before their squared modulus is taken:

A Hadamard gate followed by a computational-basis measurement realizes these $X$ statistics, since $H|\pm ⟩=|0⟩,|1⟩$, respectively. Compare the two bases using fresh, identically prepared copies: a preceding measurement may change the state. The quantum superposition section shows why replacing the preparation by the mixed state $\mathrm{diag}(3/4,1/4)$ keeps the $Z$ statistics but gives $p_{+}=p_{-}=1/2$ for every $\varphi$.

The usefulness of the Born rule is this conversion from linear algebra to experimental predictions: calculate overlaps in the basis actually measured, then take squared moduli. Its appealing geometry is that changing basis redistributes probability while preserving total squared norm. The same rule relates an energy eigenstate expansion to an energy measurement and a position wavefunction to a probability density.

Born's 1926 paper on quantum scattering interpreted the outgoing-wave coefficients in terms of the probabilities of collision outcomes; a corrective footnote specified proportionality to the square of the amplitude. This is a historical scattering formulation, rather than the general density matrix formula above. ^[ref]; ^[ref].

The canonical ensemble is the probability distribution for a system in thermal equilibrium with a heat bath at fixed temperature $T$, with fixed particle number and external parameters. It allows energy exchange, so individual energy measurements fluctuate. With Boltzmann constant $k_B$ and inverse temperature $\beta =1/(k_{B}T)$,The heat bath is idealized as large enough that exchanges barely change its temperature; coupling must permit equilibration while contributing negligible interaction energy. A finite heat bath approximates this description only when its temperature change is negligible over the relevant exchanges. Strong coupling or a small heat bath can require a different description.

For one two-level system at positive temperature, the Boltzmann weights are $1,e^{-\beta \Delta }$, henceAt $\beta \Delta =\ln 3$, $Z_1=4/3$ and $p=1/4$. This is a probabilistic thermal mixed state. For quantum levels, its density matrix is $\rho =(1-p)|0⟩⟨0|+p|1⟩⟨1|$. The pure state $\sqrt{1-p}|0⟩+\sqrt{p}|1⟩$ has the same energy measurement probabilities, but also has quantum coherence between the energy eigenstates. Matching those probabilities does not make the states equivalent.

The energy eigenspace at $E$ is the vector subspacewhere $H$ is the Hamiltonian operator and $I$ is the identity operator. It is nonzero exactly when $E$ is an energy eigenvalue. Its dimension is the multiplicity of that energy eigenvalue; degenerate energy levels have multiplicity greater than one. The ground-state subspace is ${\mathcal{E}}_{E_0}$, and its dimension is the ground-state degeneracy. A vector in an energy eigenspace need not be one of a specially chosen orthonormal basis of energy eigenstates.

Linearity makes the useful point immediate: if $H{\varphi }_1=E{\varphi }_1$ and $H{\varphi }_2=E{\varphi }_2$, then $H(a{\varphi }_1+b{\varphi }_2)=E(a{\varphi }_1+b{\varphi }_2)$. Every normalized nonzero combination stays in the same energy eigenspace. For a time-independent Hamiltonian operator, its evolution is multiplication by the common global phase $e^{-iEt/\hslash }$, so it is a stationary state. A quantum superposition within a degenerate energy eigenspace can change spatial shape when its coefficients are chosen differently, but its density does not subsequently beat under this unchanged Hamiltonian operator.

Across distinct energy eigenspaces, relative quantum phases evolve. For orthonormal eigenfunctions ${\varphi }_1,{\varphi }_2$ of the Hamiltonian operator with energy eigenvalues $E_1\ne E_2$, an equal-weight quantum superposition hasand position probability densityThe interference term can change local probabilities even though the Born rule assigns the same time-independent probability $1/2$ to each energy measurement outcome. Orthogonality makes its integral zero, preserving wavefunction normalization. This pure state is not a stationary state; some particular measurement distributions may nevertheless remain constant. An incoherent mixed state with the same energy populations has no such interference term.

For the pictured infinite square well, $\theta =3E_{1}t/\hslash$ and the interference repeats after $T=2\pi \hslash /(3E_1)$. At $t=0$, direct integration gives $⟨x⟩=L/2-16L/(9{\pi }^2)$; halfway through the period it is $L/2+16L/(9{\pi }^2)$. This is a moving expectation value, rather than a trajectory of an individual particle. The distinction between an energy eigenspace and a combination of different energy eigenspaces is what makes the different behavior possible.

An energy eigenstate is a quantum state represented by an eigenvector of the Quantum Hamiltonian. For a time-independent Quantum Hamiltonian, a normalized eigenfunction $\varphi$ with energy eigenvalue $E$ evolves according to the Schrödinger equation asHere $\hslash =h/(2\pi )$ is the reduced Planck constant. The changing factor is a global phase, so this is a stationary state: its position probability density is constant. For example, the second infinite square well mode has two density lobes separated by a node of a standing wave at $x=L/2$; both lobes stay fixed while its quantum phase rotates. An ideal energy measurement returns $E$ with probability one, but a position measurement still has a distribution. Stationary density does not describe a particle sitting at the peak of a lobe. Distinct energy eigenvalues accumulate different quantum phases, making their quantum superposition behave differently.

An energy eigenvalue is an eigenvalue of the Hamiltonian operator $H$: there is a nonzero vector $\psi$ in its operator domain $D(H)$ withFor a self-adjoint operator, $E$ is real. Normalizing $\psi$ produces an energy eigenstate; an ideal energy measurement then returns $E$ with probability one. The associated energy eigenspace includes all vectors with this same energy eigenvalue, including the zero vector, which represents no quantum state. Different energy eigenvalues have orthogonal energy eigenspaces. ^[ref].

The energy eigenvalues form the point spectrum, which can be only part of the spectrum. The term discrete spectrum more specifically means isolated eigenvalues of finite multiplicity. The usual fixed-nucleus hydrogen atom model has discrete negative bound state energy eigenvalues together with a continuum at nonnegative energy. ^[ref]. A quantum system need not have a ladder of discrete energy eigenvalues: a whole-line free particle has continuous spectrum. A plane wave used for a free particle is a generalized eigenfunction of the Hamiltonian operator, rather than a normalized vector in the physical Hilbert space. ^[ref].

For the infinite square well $0<x<L$, the Dirichlet boundary conditions giveSubstitution into $H{\varphi }_n=E_n{\varphi }_n$ and wavefunction normalization verify these statements directly. Here $E_1$ is the ground-state energy, even though its index is one; the labeling convention does not determine which quantum state is lowest. Equal populations of ${\varphi }_1$ and ${\varphi }_2$ have energy expectation value $(E_1+E_2)/2=5E_1/2$, but an energy measurement returns $E_1$ or $4E_1$, each with probability $1/2$. An average of allowed energy eigenvalues need not itself be an energy eigenvalue.

The first moment of the energy measurement distribution. For discrete energy eigenstates it is ${\sum }_n{E}_n|c_n{|}^2$ when finite; a normalizable state need not have a finite value.

Suppose a constant Hamiltonian operator has a complete discrete orthonormal basis of energy eigenstates, $H|n⟩=E_n|n⟩$. Expanding an initial pure state and applying the time-evolution operator term by term givesA projective measurement resolving these basis vectors therefore assigns the same Born rule probability $|c_n{|}^2$ to each label $n$ at every time. An energy measurement groups labels sharing the same energy eigenvalue: $P(E)={\sum }_{n:E_n=E}|c_n{|}^2$ is also constant. If $c_m,c_n\ne 0$, their probability amplitude ratio instead evolves asOnly energy differences enter this relative quantum phase. Adding a constant $\epsilon I$ to the Hamiltonian operator multiplies the entire pure state by $e^{-i\epsilon t/\hslash }$, a global phase, and leaves the density operator unchanged.

For a fixed observable $A$, the expectation value can nevertheless vary:Terms joining distinct energy eigenvalues can oscillate; diagonal terms cannot. If $[A,H]=0$, these terms between different energies vanish, so the expectation value is constant. This distinguishes conservation of energy from the stronger claim that every observable is stationary.

An energy eigenstate has only a global phase evolution and is a stationary state. A quantum superposition entirely within one degenerate energy eigenspace is also an energy eigenstate and is stationary. For a general density operator in finite dimension, stationarity under a constant Hamiltonian operator means $[H,\rho ]=0$: differentiating $U\rho U^{†}$ proves necessity, and commuting $\rho$ through the exponential proves sufficiency. Merely fixing the diagonal energy populations does not fix the off-diagonal quantum coherence.

When a ground state exists, its ground-state degeneracy is the dimension of the ground-state subspace:Here $I$ is the identity operator, and the kernel of a linear map is taken within the operator domain of the Hamiltonian operator $H$. The count concerns linearly independent energy eigenstates, rather than every normalized quantum superposition or every choice of global phase. Even a single energy eigenspace contains infinitely many representing vectors; its dimension measures independent freedom. Ground-state degeneracy is the lowest-energy instance of degenerate energy levels.

For an exact finite model with energy unit $\epsilon >0$, let the Hamiltonian operator be the diagonal matrixIts ground-state energy is zero and $g_0=2$: the first two coordinate unit vectors $e_1,e_2$ span the ground-state subspace. Every normalized $a{e}_1+b{e}_2$, with $|a{|}^2+|b{|}^2=1$, is a ground state, including $(e_1+e_2)/\sqrt{2}$. Its energy measurement is certain to return zero, even though a measurement distinguishing $e_1$ from $e_2$ need not have a definite outcome. Under the unchanged Hamiltonian operator, this quantum superposition is a stationary state because both components acquire the same global phase.

Ground-state degeneracy matters when an interaction selects or splits previously equal energy eigenvalues. In the finite model, adding $\epsilon \mathrm{diag}(\delta ,-\delta ,0,0)$ with $0<\delta <2$ gives the formerly lowest pair the distinct energies $\pm \epsilon \delta$, leaving a unique ground state. This direct calculation illustrates why degenerate perturbation theory first examines the perturbation inside the whole ground-state subspace.

A classical continuous-symmetry model can instead have a manifold of minimizing configurations, such as the sphere of orientations of a Néel state in an isotropic Heisenberg antiferromagnet. That geometric description does not by itself count the dimension of a finite quantum ground-state subspace.

The probability that an energy measurement selects a ground state. For a nondegenerate normalized mode ${\varphi }_1$, it is $|⟨{\varphi }_1,\psi ⟩{|}^2$; for a degenerate ground eigenspace, use its full orthogonal projection.

The infinite square well is an ideal confinement model with potential energy $V(x)=0$ for $0<x<L$ and infinite walls outside. The walls impose Dirichlet boundary conditions $\varphi (0)=\varphi (L)=0$ and a vanishing exterior wavefunction. Inside, the time-independent Schrödinger equation isThe first wall removes the cosine term; the second requires $\sin (kL)=0$, hence $k=n\pi /L$. The $n=0$ solution is identically zero and cannot satisfy wavefunction normalization. Each energy eigenstate has $n-1$ interior nodes of a standing wave, at $x=jL/n$ for $j=1,\dots ,n-1$. More curvature costs more kinetic energy, explaining the $n^2$ growth. The positive ground-state energy is a confinement effect: a constant zero-energy wavefunction cannot satisfy both walls and remain normalized.

For an electron with mass $m_e=9.1093837139\times 10^{-31}\mathrm{kg}$ in a box of length $L=1\mathrm{nm}$, use $h=6.62607015\times 10^{-34}\mathrm{J}\mathrm{s}$ and $1\mathrm{eV}=1.602176634\times 10^{-19}\mathrm{J}$. These constants are from the 2022 CODATA adjustment. ^[ref]. Substitution givesDoubling $L$ quarters every energy eigenvalue; doubling $m$ halves them. This scaling makes the particle in a box useful for estimating confinement energies before attempting a more realistic calculation. A finite square well permits exterior tails for bound states and has only finitely many bound energy eigenstates. For an electron, the scalar box calculation assumes fixed spin and no spin-dependent interactions.

For the ground state, the probability of finding the particle in the middle half of the box is fully computable:Thus half the available length contains about $81.8\%$ of the probability. The figure contrasts the signed wavefunctions with their nonnegative probability densities: a negative lobe is an amplitude with opposite quantum phase, not negative probability.

An equal quantum superposition of the first two energy eigenstates gives a simple example of moving density:Its density period is $T=h/(E_2-E_1)\approx 3.66608\mathrm{fs}$ for the electron box above. At $t=0$ the cross term enhances the left side; at $T/4$ it vanishes; at $T/2$ it enhances the right side. More quantitatively,which takes the values $0.924413$, $0.5$, and $0.075587$ at those times. Orthogonality keeps the total probability one throughout. An energy measurement still returns $E_1$ or $E_2$ with equal probabilities: changing position density arises from relative quantum phase, not changing populations. A mixed state describing a statistical mixture with those populations has the constant probability density $({\varphi }_1^2+{\varphi }_2^2)/2$; it lacks this matter-wave interference term.

Use the normalized eigenfunctions of the infinite square well,The sine identity expands the initial wavefunction asThe normalization factor $4/\sqrt{5a}$ yields precisely these coefficients. By the Born rule, the energy measurement probabilities are $9/10$ for $E_1$ and $1/10$ for $E_3=9E_1$. Thus the energy expectation isThe two probabilities sum to one, also checking the wavefunction normalization.

A stationary state has the formFor a time-independent quantum observable $Q$, the global phases cancel in the expectation value:It is therefore independent of time.

For the infinite square well,The possible energy measurement results arewith respective Born rule probabilities $|c_1{|}^2$ and $|c_2{|}^2$. Normalization gives $|c_1{|}^2+|c_2{|}^2=1$.

At time $t$,The required matrix elements areConsequentlywhere the angular frequency isFinally, $2|c_1{c}_2|\le |c_1{|}^2+|c_2{|}^2=1$, so

The specified initial state is normalized. The requested energy is $E_2$, and its probability amplitude isThus the Born rule givesUnitary evolution changes each energy coefficient only by a phase, so this probability remains $1/2$ at both $T$ and $2T$. If an energy measurement returns $E_2$, the state collapses to the nondegenerate eigenstate ${\chi }_2$; a subsequent energy measurement therefore returns $E_2$ with probability

The measured energy selects $n=3$. Immediately after an ideal projective measurement, the normalized state is ${\psi }_3(x)$ up to an overall phase, with no surviving $n=1,2,4$ components. At later times before any further disturbance it is $e^{-i9c(t-t_0)/\hslash }{\psi }_3(x)$, where $t_0$ is the measurement time. A repeated energy measurement returns $9c$ with probability one.

Time dependence in quantum mechanics describes how a prepared quantum state changes and thereby changes the probabilities of later measurements. For an isolated system, the Schrödinger picture assigns this evolution to a state vector $|\psi (t)⟩$, governed by the Time-dependent Schrödinger equationThe Hamiltonian is a self-adjoint operator; it has units of energy, while $\hslash$ has units of action, so $\hat{H}/\hslash$ has units of inverse time. For a particle with potential energy $V(\mathbf{r},t)$, this becomesGiven a suitable initial wavefunction and the physical boundary conditions, this first-order equation determines its subsequent propagation. Its linearity means that the evolution of a quantum superposition is the corresponding quantum superposition of evolved states.

For a real potential energy, this equation and its complex conjugate imply the local continuity equationHere $\rho$ is the probability density and $\mathbf{j}$ the probability current. Vanishing net boundary flux preserves wavefunction normalization, as required by the Born rule.

The time-evolution operator packages the solution for every initial state:Because ${\hat{H}}^{†}=\hat{H}$, differentiation givesTherefore $U^{†}U=I$: this is unitary time evolution, preserving inner products and all state norms. It is reversible, with $U(t,t_0{)}^{-1}=U(t_0,t)=U(t,t_0{)}^{†}$, and obeys the composition law $U(t_2,t_0)=U(t_2,t_1)U(t_1,t_0)$.

For a time-independent Hamiltonian, the solution is the operator exponentialIf the Hamiltonian varies with time, the analogous simple exponential of its integral is valid when $[\hat{H}(t),\hat{H}(t^{\prime })]=0$ for all relevant times. Otherwise time ordering is essential:The meaning is explicit in the first terms of the ordered series,the later-time operator stands on the left. In the position representation, the same propagation is expressed by the quantum-mechanical propagatorIts initial value is the Dirac delta function ${\delta }^3(\mathbf{r}-{\mathbf{r}}^{\prime })$.

A time-independent Hamiltonian has energy eigenstates satisfying $\hat{H}|n⟩=E_n|n⟩$. A single such initial state evolves asIt is a stationary state: its global phase changes, but its probability density and the distributions of time-independent observables do not. Its energy is sharp. Any quantum superposition entirely within one degenerate energy eigenspace also acquires one common global phase and is stationary. Stationarity does not require zero probability current; for instance, $u_n(\varphi )=e^{in\varphi }/\sqrt{2\pi }$ on the ring has a constant density and persistent circulation when $n\ne 0$.

An arbitrary normalized state can instead contain different energy eigenvalues:A continuous spectrum requires corresponding integrals. For the discrete case, an energy measurement gives $E_n$ with fixed probability $|c_n{|}^2$ (summed over degeneracies), but relative quantum phases change with time. ConsequentlyThe interference terms can oscillate at angular frequencies $(E_m-E_n)/\hslash$. For two populated energy levels, this supplies a characteristic period $2\pi \hslash /|E_m-E_n|$ when the interference term is nonzero. Thus fixed energy populations do not imply a stationary spatial distribution.

For a normalized state and an observable $\hat{A}(t)$, its expectation value isThis is the statistical mean over repeated preparations and measurements. In an eigenbasis of energy eigenstates for a time-independent Hamiltonian and a time-independent $\hat{A}$,Only matrix elements connecting different energies can generate these oscillations. If $[\hat{A},\hat{H}]=0$, its expectation value is constant for every initial state, provided it has no explicit time dependence.

Differentiating the expectation value and substituting the Schrödinger equation for both the bra and ket proves the general Ehrenfest theorem:Equivalently,These manipulations require the state to lie in the relevant operator domains. Taking $\hat{A}=\hat{H}$ gives $d⟨H⟩/dt=⟨{\partial }_t\hat{H}⟩$, so energy is conserved under a time-independent Hamiltonian.

For $\hat{H}={\hat{p}}^2/(2m)+V(\hat{x})$, the canonical commutation relation givesHence the particularly useful position-and-momentum form of Ehrenfest theorem isIt resembles Newton's second law, but the mean force generally differs from the force at the mean position. If a narrow wave packet samples a region where the force varies little, $⟨V^{\prime }(x)⟩\simeq V^{\prime }(⟨x⟩)$ gives approximate classical motion. For a quadratic potential energy this replacement is exact. In particular the quantum harmonic oscillator obeysThe centroid follows the classical harmonic oscillator, although this does not specify the full evolving wavefunction or its width.

The Heisenberg picture expresses the same physics by assigning evolution to observables instead:The expectation value is unchanged, and differentiation yields $d{\hat{A}}_H/dt=(i/\hslash )[{\hat{H}}_H,{\hat{A}}_H]+U^{†}({\partial }_t{\hat{A}}_S)U$. Thus state propagation, evolving expectation values, and the classical correspondence in Ehrenfest theorem are mutually consistent descriptions of the same unitary time evolution.

Write $k=\pi /a$, $A=\sqrt{2/a}$ and ${\Psi }_0=A{e}^{ikx}\sin kx$. Its derivative isIntegration by parts with the Dirichlet boundary conditions gives the energy expectationIt is constant in time, since the time-independent Hamiltonian operator has fixed energy measurement probabilities: $⟨H{⟩}_t={\sum }_n{E}_n|c_n{|}^2$.

For the midpoint parity operator, $R{\Psi }_0=-A{e}^{-ikx}\sin kx$. Hence, again putting $u=kx$,Indeed the imaginary part integrates to zero by reflection and ${\int }_0^{\pi }\cos 2u{\sin }^{2}udu=-\pi /4$. This expectation value is also constant in time, because the bounded self-adjoint operator $R$ commutes with $H$ and hence with its time-evolution operator. Equivalently, $⟨R{⟩}_t={\sum }_n(-1{)}^{n+1}|c_n{|}^2$.

For the momentum operator, direct evaluation givesThe real sine-cosine integral vanishes. This expectation value is not constant in time: the infinite square well walls reverse motion. One can prove the change exactly without approximating the wavefunction. Atthe energy eigenstate expansion and $R{\psi }_n=(-1{)}^{n+1}{\psi }_n$ give $\Psi (t_{\ast })=-R{\Psi }_0$. Differentiation shows $PR=-RP$, soThis half revival in an infinite square well is a concrete counterexample to momentum conservation. The sign from $-R$ is only a global phase.

The apparent interior identity $[H,P]=0$ cannot justify conservation here: the momentum operator does not preserve the Dirichlet boundary conditions of the Hamiltonian operator's operator domain. For sufficiently regular states, retaining the boundary terms in Ehrenfest theorem instead gives the boundary force in an infinite square well,In the strictly confined interval, $-i\hslash {\partial }_x$ with both endpoint values zero is symmetric but not itself a self-adjoint operator. The requested integral is the conventional mean momentum; it also equals the full-line momentum mean of the zero-extended state, as measured upon releasing the walls. This domain distinction explains why the formal interior commutator misses the wall force.

The requested energy eigenvalue is $E_2$. By the Born rule, its probability amplitude is the inner product $c_2=⟨{\psi }_2,\Psi (0)⟩$. Put $u=\pi x/a$ and use $e^{iu}\sin u=\frac{1}{2}\sin 2u+i{\sin }^{2}u$:The first integral is $\pi /2$; the second is zero under $u\mapsto \pi -u$. ThereforeFor the time-independent Hamiltonian operator, expand in its orthonormal basis of energy eigenstates:Unitary time evolution changes $c_2$ to $c_2{e}^{-i{E}_{2}t/\hslash }$, whose modulus is unchanged. Thus the same energy measurement probability holds at every time, even though relative quantum phases and other measurements can change.

Put $\gamma =2m\hslash \omega$. If ${\psi }_n$ is a normalized energy eigenstate at $E_n$, the factorization from part (a) givesIt follows inductively that $v_n=(a_{+}{)}^n{\psi }_0$ has squared norm ${\gamma }^{n}n!$. The commutator with $H$ establishes its energy eigenvalue at each step. Henceis normalized and has $E_n=(n+\frac{1}{2})\hslash \omega$. Distinct levels are orthogonal because $H$ is a self-adjoint operator. In particular,

To decompose the specified initial wavefunction, retain this exact phase convention for the creation and annihilation operators. Their difference givesSince $a_{-}{\psi }_0=0$ and $a_{-}{a}_{+}{\psi }_0=\gamma {\psi }_0$,This quadratic excitation of an oscillator ground state, $\Psi (x,0)=C_0^{-1}{X}^2{\psi }_0$, contains only the $n=0$ and $n=2$ energy eigenstates. The printed initial function has an unspecified overall normalization, so the Born rule requires division by its squared norm. After wavefunction normalization the state isThe minus sign is consistent with the paper's convention: its $a_{+}$ is $i$ times the usual real-coordinate raising operator multiplied by $\sqrt{\gamma }$, so its ${\psi }_2$ has the opposite sign to the usual real second harmonic oscillator eigenfunction. The energy measurement probabilities are independent of this choice of phase.