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For emission take integers $n_i>n_f\ge 1$. Applying conservation of energy to the model's internal energy difference, while neglecting the much smaller whole-atom photon recoil, givesThus Johannes Robert Rydberg's Rydberg formula is a difference of two energy levels expressed as a spectroscopic wavenumber. The same constants determine every line; there is no new parameter for each electronic transition. With the chosen inputs, $R_H=1.096775834\times 10^7{\mathrm{m}}^{-1}$. All wavelengths below are calculated in vacuum, not air, and are rounded model predictions rather than historical measurements.

The conventional names commemorate Theodore Lyman and Johann Jakob Balmer. Fixing $n_f=1$ produces the ultraviolet Lyman series, beginning with the Lyman-alpha line; fixing $n_f=2$ produces the Balmer series. As $n_i\to \infty$, the wavelength approaches $n_f^2/R_H$: $91.1763\mathrm{nm}$ at the Lyman limit and $364.705\mathrm{nm}$ for the Balmer series. Crowding follows directly from $E_{n+1}-E_n\sim 2B_H/n^3$. Discreteness therefore coexists with a series limit.

Correct line positions do not give wave intensities, lifetimes or electric-dipole selection rules for hydrogen. Those require a theory of the wavefunctions and their coupling to electromagnetic radiation. The circular model also omits spin, relativistic corrections and the Lamb shift. Its successful gross energy levels do not make its assumed orbits modern atomic orbitals.

An impurity level is an electronic energy level associated with a dopant or defect in a semiconductor. A shallow donor impurity introduces a level just below the conduction band, and a shallow acceptor impurity introduces one just above the valence band. Under electrostatic band bending, these levels shift with the local band edges in the same material; their occupation is determined relative to the equilibrium chemical potential.

Consider an explicitly stipulated dilute independent spin-one-half two-level system with zero applied magnetic field. Each constituent has $J_z=\pm \hslash /2$ and $m_z=\gamma J_z$, with constant signed gyromagnetic ratio $\gamma$. Ignore interactions and the specimen's own magnetic field. At positive temperature $T$, thermal equilibrium with the rotating lattice gives energy levels $E_{\pm }=\mp \hslash \Omega /2$. Define the dimensionless variable $x=\hslash \Omega /(2k_{B}T)$, where $\hslash$ is the reduced Planck constant and $k_B$ is the Boltzmann constant. The partition function and Boltzmann distribution giveTaking the expected value giveswhere $n$ is number density. This is the rotational version of the independent-moment magnetic response. The angular momentum aligns with positive rotation even when the magnetic moment points oppositely. The probability ratio $p_{+}/p_{-}=e^{2x}$ provides a direct population check of the sign.

For $|x|\ll 1$, expand the hyperbolic tangent to obtainThe slope against $B_{\Omega }$ is positive for either sign of $\gamma$, while the slope against $\Omega$ has the sign of $\gamma$. At fixed $T>0$, reversing $\Omega$ reverses both means, and $\Omega =0$ gives zero. At fixed nonzero $\Omega$, the formal $T\to 0^{+}$ limit saturates $|⟨J_z⟩|$ at $\hslash /2$; the linear approximation must not be extrapolated there. At $T\to \infty$, the response vanishes. These limits describe the toy canonical ensemble, whose equilibration is assumed.

For a numerical example, stipulate $n=10^{28}{\mathrm{m}}^{-3}$, $T=300\mathrm{K}$, $\gamma =-1.76\times 10^{11}{\mathrm{s}}^{-1}{\mathrm{T}}^{-1}$, and rotation frequency $f=1000\mathrm{Hz}$. With $\Omega =2\pi f$, $\hslash =1.054571817\times 10^{-34}\mathrm{J}\mathrm{s}$, and $k_B=1.380649\times 10^{-23}J/K$, the model givesThese are teaching inputs and calculated outputs, not measured material values. The corresponding internal angular momentum density is $M_z/\gamma =+4.22\times 10^{-17}\mathrm{J}s/{\mathrm{m}}^3$. Keeping a rotor at prescribed $\Omega$ while its internal angular momentum changes requires the drive to supply the appropriate angular impulse. In an isolated body the mechanical part instead changes oppositely, as in magnetomechanical angular momentum balance. There is no creation of net angular momentum by choosing a rotating frame.

An ion trap confines an ion using electromagnetic fields, allowing repeated interrogation of the same particle. The name also covers related traps for an Electron. A Paul trap uses an oscillating electric quadrupole field; a Penning trap combines a static electric quadrupole field with a static magnetic field. Confinement creates time to measure an energy level, frequency or magnetic dipole moment; it does not itself cool the particle or identify its internal quantum state.

The obstacle is Earnshaw's theorem. In a charge-free neighbourhood the static electric potential $\Phi$ obeys Laplace's equation, ${\nabla }^2\Phi =0$. For a particle of fixed nonzero electric charge $Q$, the potential energy $Q\Phi$ is also a harmonic function. The maximum principle for harmonic functions excludes a strict interior minimum. For a quadratic example, the Hessian matrix has zero trace; it cannot have three positive eigenvalues. A static purely electric field therefore cannot supply three-dimensional stable confinement of a free point electric charge. Time variation in a Paul trap, and the velocity-dependent Lorentz force in a Penning trap, change the assumptions of this argument.

A Josephson junction couples two regions with superconductivity through a weak link. A tunnel barrier is one implementation.

The remarkable possibility is a steady electric current across an insulating barrier at zero electric potential difference. This is the DC Josephson effect, carried by coherent transfer of Cooper pairs. It differs from single-electron superconducting tunneling, which probes the quasiparticle excitation spectrum and produces a dissipative current-voltage characteristic. Both contributions can occur in the same superconducting tunnel device. Brian D. Josephson predicted the pair contribution in 1962; his paper treats transfer that leaves the quasiparticle distribution unchanged. ^[ref]

The Josephson effect turns a difference of quantum phases into a measurable electric current, and an applied electric potential difference into a rate of phase advance. The Giaever gap experiment instead turns an electric potential difference into an excitation energy scale. These complementary measurements expose two aspects of superconductivity: its coherent order parameter and its gapped quasiparticle spectrum. The microscopic pairing calculation belongs to BCS theory and the BCS gap equation. A tunnel diode uses a different device, a semiconductor p-n junction.

Adding capacitance and an external bias makes the Gauge-invariant Josephson phase dynamical. Current-biased Josephson phase dynamics explains how its trapped energy levels and escape can be measured electrically.

A quantum electrodynamics correction separates hydrogen atom levels such as $2s_{1/2}$ and $2p_{1/2}$ that coincide in the simplest model.

The Lamb shift measures an energy level displacement beyond a specified Dirac equation reference. In the point-proton, infinite-nuclear-mass Coulomb potential model, $2S_{1/2}$ and $2P_{1/2}$ share principal quantum number $n=2$ and total electronic angular momentum $j=1/2$, hence energy, despite differing orbital angular momentum values.^[ref]

The Lamb-Retherford experiment converts a small energy difference into a large detector change: prepare a long-lived quantum state, transfer population into a short-lived one, and read the surviving beam.

A transition during a sweep through an avoided crossing of energy levels.

Laser spectroscopy uses a tunable laser to interrogate energy levels through photon absorption, stimulated emission or fluorescence. A narrow optical source is useful only if the sample and readout preserve the information: Doppler broadening can hide closely spaced spectral lines even when the source itself is narrow.

Magnetic entropy counts the uncertainty in the occupied magnetic microstates. For independent localized magnetic moments with one-site probabilities $p_j$,where $N$ counts sites and $k_B$ is the Boltzmann constant. This is the Gibbs entropy for the magnetic degrees of freedom. Equal occupation of two states gives $N{k}_B\ln 2$; certain occupation of one state gives zero. Calling this disorder is useful only if the relevant states and their probabilities are specified. In an interacting material, correlations generally prevent replacing the many-body Gibbs entropy by this sum of independent one-site contributions.

Increasing the magnetic field at fixed positive temperature favors lower magnetic energy levels, reducing magnetic entropy. During ideal isolated demagnetization, both the level separation and temperature fall together, leaving the occupation probabilities unchanged. Thus the independent-spin idealization cools without increasing spin disorder along the isolated leg. When a real crystal's vibrating lattice also cools, its lost entropy can instead be taken up by the magnetic degrees of freedom. The conserved quantity is the total entropy of the thermally isolated stage, including any attached load in thermal equilibrium.

One of the angular momentum eigenstates in a multiplet, distinguished by the magnetic quantum number along a chosen axis. An applied magnetic field can split their energy levels through Zeeman splitting.

The 1985 spectroscopy experiment used niobium-based tunnel Josephson junctions on silicon, thermally anchored with final bias low-pass filters to a dilution refrigerator. Calibrated germanium and cobalt thermometers measured temperature. A filtered coaxial cable injected microwaves; repeated switches to nonzero electric potential difference measured escape with irradiation on and off. Bias scans at fixed microwave frequency resolved separate enhancements matching calculated unequal energy level spacings. Raising temperature merged the structure toward classical response. Junction parameters were calibrated in the classical regime; reducing the superconducting critical current with a magnetic field checked thermal readout. Parameter uncertainties limited absolute resonance positions.^[ref]

The companion escape experiment mounted a tunnel Josephson junction on an attenuating coaxial cable, cold-anchored its bias filters, ramped the electric current, and counted switches to nonzero electric potential difference. Rapid current shutoff limited heating. Classical escape and microwave resonance calibrated the superconducting critical current, capacitance and environmental loading. Low-temperature escape agreed with the quantum prediction using these calibrated parameters. A magnetic field reduced the superconducting critical current to keep the same apparatus thermally activated at lower temperature, testing excess noise. Frequency-dependent loading contributed uncertainty; the predicted damping correction was smaller than combined errors, so the experiment did not resolve that correction.^[ref]

Together these tests connect spectral structure and escape of the same kind of collective coordinate. They do not constitute a demonstration of coherent gate operations on a qubit, or prove that every macroscopic coordinate retains quantum behavior under arbitrary environmental coupling. The attraction is more concrete: a fabricated electrical circuit admits both an independently measurable classical model and quantitative quantum tests of its phase dynamics.

A maser uses stimulated emission to amplify microwaves. With population inversion and feedback it can sustain a coherent wave field as an oscillator. The name abbreviates "microwave amplification by stimulated emission of radiation".^[ref]

Why make molecules supply an oscillator? Their energy levels offer a reproducible frequency reference, while stimulated emission lets successive molecules reinforce one coherent wave field. In his 1964 lecture, Charles Hard Townes traced his motivation to microwave spectroscopy: resolving molecular structure required useful coherent sources.^[ref] The interesting balance is between molecular amplification and escaping energy: even a beam with population inversion fails to oscillate if cavity losses win. This is the microwave counterpart of laser threshold.

Maser state selection separates paths according to the Stark effect, the dependence of a molecule's energy levels on an electric field. It prepares a transmitted population by sorting. Optical pumping, by contrast, changes populations through absorption of light and subsequent transitions. Both can produce a useful population imbalance, but they are different preparation mechanisms.

A simple two-level system explains the sign of the focusing force. Ignore additional splittings and let the magnitude of the relevant projected electric dipole moment be $d$. Model the two local energy levels in an electric field of magnitude $\mathcal{E}$ byFor an ideal quadrupolar electrostatic potential $\Phi =A(x^2-y^2)$, the electric field magnitude is $\mathcal{E}=2|A|r$, where $r=\sqrt{x^2+y^2}$. Since $W_{+}$ increases with $r$, the force ${\mathbf{F}}_{+}=-\nabla W_{+}$ points inward. The lower branch has the opposite sign and is defocused. The upper branch is thus low-field seeking. This argument uses the gradient of internal energy, rather than a net electric charge on the molecule. The square-root splitting is the usual two-state description.^[ref] The idealized two-level system omits the actual rotational and hyperfine structure sublevels and their different transmission efficiencies.

Matrix mechanics represents an observable by an array of matrix elements between chosen quantum states. In an orthonormal basis of energy eigenstates, each a stationary state, the diagonal entries of the Hamiltonian operator are the energy levels; off-diagonal entries of other observables describe couplings between those states. The same array can therefore answer two different questions: which values can a measurement return, and which pairs of energy eigenstates can a specified interaction connect? The eigenvalues answer the first question; the relevant matrix elements, together with the energy differences, answer the second.

This makes linear algebra a practical language for atomic physics. One can calculate energy levels, electric-dipole selection rules and probability amplitudes for transitions without assigning an Electron an unobserved classical orbit. The three-state example below separates a missing optical coupling from a missing energy level; the finite oscillator commutator boundary defect explains why a finite array requires care when approximating a quantum harmonic oscillator.

A motional sideband is a transition that changes internal excitation and a motional quantum number together. Define the internal energy gap as $\hslash {\omega }_0>0$. A carrier drives $|g,n⟩\leftrightarrow |e,n⟩$; the first red sideband drives $|g,n⟩\leftrightarrow |e,n-1⟩$; the first blue sideband drives $|g,n⟩\leftrightarrow |e,n+1⟩$. Their resonant drive angular frequencies follow by subtracting these energy levels. For a Raman transition, the drive is a beam-difference frequency with a sign fixed by the selected internal transition.

Choose a real carrier Rabi angular frequency $\Omega$ defined so that resonant carrier excitation is ${\sin }^2(\Omega t/2)$. In the Lamb-Dicke regime, isolated first-sideband Hamiltonians in a rotating frame can be written, after choosing the pulse phase, asThese formulas use a rotating-wave approximation: neglected carrier and other-sideband terms oscillate rapidly compared with the retained coupling. The drive's effective width and sideband coupling must be small compared with $\nu$; sufficient suppression of off-resonant carrier excitation must also be checked. The red interaction is a Jaynes-Cummings model with a motional quantum replacing a cavity photon. The blue interaction creates internal excitation and a motional quantum together; the external laser supplies energy. The driven-system rotating-frame Hamiltonian alone is not the total laboratory energy.