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Constants and Conversions

Atomic, molecular, and optical physics routinely describes one energy in joules, electronvolts, kelvin, hertz, angular frequency, inverse centimetres, and atomic units. These are not competing physical descriptions. They are different numerical coordinates on the same quantity, provided the conversion uses the correct constant and the author states whether a frequency is cyclic or angular.

This page is a versioned quick reference for those translations. Its central identity is

E=hν=ℏω=hcν~=kBTE,E =h\nu =\hbar\omega =hc\tilde{\nu} =k_{\mathrm B}T_E,

where TET_E is an energy-equivalent temperature, not automatically the thermodynamic temperature of a sample. Most factor-of-2π2\pi and factor-of-100 errors in AMO calculations can be found by returning to this line and checking the units.

This page owns the AMO-facing conversion workflow:

  • photon and transition energies in J\mathrm J, eV\mathrm{eV}, Hz\mathrm{Hz}, rad s−1\mathrm{rad\,s^{-1}}, cm−1\mathrm{cm^{-1}}, and K\mathrm K;
  • the distinction among frequency, angular frequency, wavenumber, and wavevector;
  • practical magnetic-moment and electric-dipole conversion scales;
  • rules for reporting exact, derived-exact, and measured constants; and
  • examples that expose the convention choices hidden by bare numbers.

It does not rederive Hartree atomic units. That material lives in Atomic Units and Scales and the Atomic Units reference entry. The global Constants table remains the canonical compact list of constants across all volumes, while Fundamental Constants explains how measured constants are inferred, adjusted, correlated, and updated.

The numerical values below use two different kinds of authority:

  1. The International System of Units is taken from version 4.01 of the ninth edition of the BIPM SI Brochure, updated in June 2026.
  2. Measured constants use the 2022 CODATA recommended values released by NIST in 2024 and published in full in 2025. NIST identifies this as the latest available CODATA set; the next regular adjustment is the 2026 adjustment.

The distinction matters. Since 20 May 2019, the numerical values of hh, cc, ee, and kBk_{\mathrm B} are fixed in the SI. The electron mass, fine-structure constant, Rydberg constant, Bohr magneton, and nuclear magneton remain measured or adjusted quantities. Their recommended values can change when CODATA incorporates new evidence.

This page uses the following labels.

LabelMeaningExample
exactthe numerical value is fixed by the SI definitionhh, cc, ee, kBk_{\mathrm B}
derived exactthe value follows exactly from defining constants, but its decimal expansion may not terminateℏ=h/(2π)\hbar=h/(2\pi), 1 eV1\ \mathrm{eV} in joules
measuredthe value has a standard uncertainty and may change in a future adjustmentmem_e, α\alpha, R∞R_\infty, μB\mu_{\mathrm B}

An ellipsis after a derived-exact decimal means that digits were truncated, not that the quantity has measurement uncertainty. Parentheses after a measured value have a different meaning: for example, 7.297 352 5643(11)×10−37.297\,352\,5643(11)\times10^{-3} gives a standard uncertainty of 0.000 000 0011×10−30.000\,000\,0011\times10^{-3}.

The same symbols are not used uniformly across every subfield. This page uses the following convention.

QuantitySymbolDefinitionPreferred unit
energyEEHamiltonian eigenvalue difference or photon energyJ\mathrm J or eV\mathrm{eV}
cyclic frequencyν\nu or ffcycles per unit timeHz\mathrm{Hz}
angular frequencyω\omega2πν2\pi\nurad s−1\mathrm{rad\,s^{-1}}
vacuum wavelengthλ0\lambda_0c/νc/\num\mathrm m or nm\mathrm{nm}
vacuum wavenumberν~\tilde{\nu}1/λ0=ν/c1/\lambda_0=\nu/cm−1\mathrm{m^{-1}} or cm−1\mathrm{cm^{-1}}
wavevector magnitudekk2π/λ02\pi/\lambda_0rad m−1\mathrm{rad\,m^{-1}}
energy-equivalent temperatureTET_EE/kBE/k_{\mathrm B}K\mathrm K

IUPAC recommends ν~\tilde{\nu} for vacuum wavenumber and notes that σ\sigma may be used for wavenumber in a medium. In an AMO paper, the safest practice is to define the symbol once rather than rely on local custom.

Two pairs are especially easy to confuse:

ω=2πν,k=2πν~.\omega=2\pi\nu, \qquad k=2\pi\tilde{\nu}.

Thus 1 Hz1\ \mathrm{Hz} and 1 rad s−11\ \mathrm{rad\,s^{-1}} do not represent the same numerical frequency, even though both can be reduced dimensionally to inverse seconds. Likewise, ν~\tilde{\nu} in cm−1\mathrm{cm^{-1}} is not the same quantity as the wavevector kk.

The values in this table are exact in the present SI.

ConstantSymbolSI valueAMO role
speed of light in vacuumcc299 792 458 m s−1299\,792\,458\ \mathrm{m\,s^{-1}}wavelength–frequency conversion
Planck constanthh6.626 070 15×10−34 J s6.626\,070\,15\times10^{-34}\ \mathrm{J\,s}energy per cycle frequency
reduced Planck constantℏ\hbar1.054 571 817…×10−34 J s1.054\,571\,817\ldots\times10^{-34}\ \mathrm{J\,s}energy per angular frequency
elementary charge magnitudeee1.602 176 634×10−19 C1.602\,176\,634\times10^{-19}\ \mathrm Celectronvolt and electromagnetic coupling
Boltzmann constantkBk_{\mathrm B}1.380 649×10−23 J K−11.380\,649\times10^{-23}\ \mathrm{J\,K^{-1}}energy–temperature conversion

The symbol ee denotes a positive magnitude. The electron charge is qe=−eq_e=-e. A Hamiltonian written with a particle charge qq must therefore use q=−eq=-e for an electron; silently replacing qq by ee reverses electric and magnetic signs.

Because

ℏ=h2π,\hbar=\frac{h}{2\pi},

hh belongs with cyclic frequency and ℏ\hbar belongs with angular frequency:

E=hν=ℏω.E=h\nu=\hbar\omega.

Mixing hh with ω\omega or ℏ\hbar with ν\nu inserts or removes a factor of 2π2\pi.

The following rounded values come from the 2022 CODATA adjustment. The parenthetical digits are one-standard-deviation uncertainties in the final quoted digits.

ConstantSymbol2022 CODATA value
electron massmem_e9.109 383 7139(28)×10−31 kg9.109\,383\,7139(28)\times10^{-31}\ \mathrm{kg}
fine-structure constantα\alpha7.297 352 5643(11)×10−37.297\,352\,5643(11)\times10^{-3}
inverse fine-structure constantα−1\alpha^{-1}137.035 999 177(21)137.035\,999\,177(21)
Rydberg constantR∞R_\infty10 973 731.568 157(12) m−110\,973\,731.568\,157(12)\ \mathrm{m^{-1}}
Bohr magnetonμB\mu_{\mathrm B}9.274 010 0657(29)×10−24 J T−19.274\,010\,0657(29)\times10^{-24}\ \mathrm{J\,T^{-1}}
nuclear magnetonμN\mu_{\mathrm N}5.050 783 7393(16)×10−27 J T−15.050\,783\,7393(16)\times10^{-27}\ \mathrm{J\,T^{-1}}

These constants are related, not independent entries in a bag of numbers. For example,

α=e24πϵ0ℏc,μB=eℏ2me,μN=eℏ2mp.\alpha =\frac{e^2}{4\pi\epsilon_0\hbar c}, \qquad \mu_{\mathrm B} =\frac{e\hbar}{2m_e}, \qquad \mu_{\mathrm N} =\frac{e\hbar}{2m_p}.

After the 2019 SI revision, ϵ0\epsilon_0 and μ0\mu_0 are measured quantities because they inherit the uncertainty of α\alpha. In particular, μ0=4π×10−7 N A−2\mu_0=4\pi\times10^{-7}\ \mathrm{N\,A^{-2}} is no longer exact.

The Rydberg constant describes the infinite-nuclear-mass Coulomb scale:

R∞=α2mec2h,hcR∞=13.605 693 122 990(15) eV.R_\infty =\frac{\alpha^2m_ec}{2h}, \qquad hcR_\infty =13.605\,693\,122\,990(15)\ \mathrm{eV}.

It should not be inserted as though it were the exact line wavenumber of a finite-mass atom. Reduced-mass, recoil, relativistic, radiative, nuclear-size, and hyperfine corrections separate an observed transition from the simple R∞R_\infty formula.

For a vacuum photon or an energy splitting represented by an equivalent frequency,

E=hν,=ℏω,=hcλ0,=hcν~,=kBTE.\begin{aligned} E &= h\nu,\\ &= \hbar\omega,\\ &= \frac{hc}{\lambda_0},\\ &= hc\tilde{\nu},\\ &= k_{\mathrm B}T_E. \end{aligned}

Each equality identifies the conversion constant:

  • divide by hh to convert energy to hertz;
  • divide by ℏ\hbar to convert energy to radians per second;
  • divide by hchc to convert energy to inverse length;
  • divide by kBk_{\mathrm B} to convert energy to kelvin; and
  • divide by ee to convert joules to electronvolts.

Dimensional analysis catches most mistakes:

JJ s=s−1,JJ K−1=K.\frac{\mathrm J}{\mathrm{J\,s}} =\mathrm{s^{-1}}, \qquad \frac{\mathrm J} {\mathrm{J\,K^{-1}}} =\mathrm K.

The first result is not enough to decide whether the number represents cycles per second or radians per second. That decision comes from whether the divisor was hh or ℏ\hbar.

The displayed digits below are rounded. The underlying factors are derived from exact SI defining constants, so the ellipses represent nonterminating decimal expansions rather than experimental uncertainty.

Starting quantityJoulesHertzInverse centimetresKelvin
1 eV1\ \mathrm{eV}1.602 176 634×10−191.602\,176\,634\times10^{-19}2.417 989 242 085×10142.417\,989\,242\,085\times10^{14}8 065.543 937 3498\,065.543\,937\,34911 604.518 121 5511\,604.518\,121\,55
1 cm−11\ \mathrm{cm^{-1}}1.986 445 857 149×10−231.986\,445\,857\,149\times10^{-23}2.997 924 58×10102.997\,924\,58\times10^{10}111.438 776 877 5041.438\,776\,877\,504
1 Hz1\ \mathrm{Hz}6.626 070 15×10−346.626\,070\,15\times10^{-34}113.335 640 951 982×10−113.335\,640\,951\,982\times10^{-11}4.799 243 073 366×10−114.799\,243\,073\,366\times10^{-11}
1 K1\ \mathrm K1.380 649×10−231.380\,649\times10^{-23}2.083 661 912 333×10102.083\,661\,912\,333\times10^{10}0.695 034 800 4860.695\,034\,800\,48611

For electronvolts and kelvin,

1 K=8.617 333 262 145×10−5 eV,1\ \mathrm K =8.617\,333\,262\,145\times10^{-5}\ \mathrm{eV},

and therefore

1 meV≈11.6045 K.1\ \mathrm{meV} \approx11.6045\ \mathrm K.

For wavenumbers,

1 cm−1=29.979 2458 GHz.1\ \mathrm{cm^{-1}} =29.979\,2458\ \mathrm{GHz}.

This exact frequency factor follows from cc and the exact relation 1 cm−1=100 m−11\ \mathrm{cm^{-1}}=100\ \mathrm{m^{-1}}.

The electronvolt is the energy acquired by a charge of magnitude ee through an electric potential difference of one volt:

1 eV=e×1 V=1.602 176 634×10−19 J.1\ \mathrm{eV} =e\times1\ \mathrm V =1.602\,176\,634\times10^{-19}\ \mathrm J.

Its SI value is exact because ee is a defining constant. The electronvolt is not a volt, and an energy in electronvolts should not be divided by ee a second time.

Useful scale markers are:

RegimeTypical energy
radiofrequency and microwave hyperfine controlneV\mathrm{neV} to μeV\mathrm{\mu eV}
molecular rotationμeV\mathrm{\mu eV} to meV\mathrm{meV}
molecular vibrationmeV\mathrm{meV} to tenths of an eV\mathrm{eV}
visible atomic and molecular transitionsroughly 11–4 eV4\ \mathrm{eV}
core-electron and x-ray transitionskeV\mathrm{keV} and above

These ranges orient a calculation; they are not classification boundaries.

Spectroscopists often report an energy as a vacuum wavenumber:

ν~=1λ0=νc=Ehc.\tilde{\nu} =\frac{1}{\lambda_0} =\frac{\nu}{c} =\frac{E}{hc}.

The common unit cm−1\mathrm{cm^{-1}} is an inverse length, not “per centimetre of path traveled” and not an angular wavevector. Because 1 cm−1=100 m−11\ \mathrm{cm^{-1}}=100\ \mathrm{m^{-1}},

E=hc(100ν~[cm−1])E =hc\left(100\tilde{\nu}_{[\mathrm{cm^{-1}}]}\right)

when ν~[cm−1]\tilde{\nu}_{[\mathrm{cm^{-1}}]} is the numerical value quoted in cm−1\mathrm{cm^{-1}}.

For a vacuum wavelength expressed in nanometres,

ν~ [cm−1]=107λ0 [nm].\tilde{\nu}\,[\mathrm{cm^{-1}}] =\frac{10^7} {\lambda_0\,[\mathrm{nm}]}.

A reported wavelength must say whether it is a vacuum wavelength or an air wavelength. Frequency is continuous across a stationary interface, while the wavelength in a medium is

λmed=λ0n(ν).\lambda_{\mathrm{med}} =\frac{\lambda_0}{n(\nu)}.

At low precision, “589 nm” may be enough context. At precision-spectroscopy accuracy, the refractive-index model, pressure, temperature, humidity, and composition of the medium can matter.

NIST recommends explicit units because the numerical values of frequency and angular frequency differ by 2π2\pi:

ω=2πν.\omega=2\pi\nu.

Use hertz for cyclic frequency and radians per second for angular frequency:

ν=ΔEh,ω=ΔEℏ.\nu=\frac{\Delta E}{h}, \qquad \omega=\frac{\Delta E}{\hbar}.

This distinction propagates into time evolution. A stationary amplitude contains

e−iEt/ℏ=e−iωt=e−i2πνt.e^{-iEt/\hbar} =e^{-i\omega t} =e^{-i2\pi\nu t}.

The same issue appears in detunings, Rabi frequencies, decay rates, and linewidths. A statement such as “Ω=10 MHz\Omega=10\ \mathrm{MHz}” is incomplete unless the convention is established. Two unambiguous alternatives are

Ω2π=10 MHz\frac{\Omega}{2\pi}=10\ \mathrm{MHz}

and

Ω=10 Mrad s−1.\Omega=10\ \mathrm{Mrad\,s^{-1}}.

They describe different angular frequencies by a factor of 2π2\pi.

A decay rate Γ\Gamma is often written in s−1\mathrm{s^{-1}}, while a spectral linewidth may be quoted in Hz\mathrm{Hz} or rad s−1\mathrm{rad\,s^{-1}}. Under the standard isolated, lifetime-limited two-level convention in which the excited population decays as e−Γte^{-\Gamma t}, the Lorentzian full width at half maximum is

ΔωFWHM=Γ,ΔνFWHM=Γ2π.\Delta\omega_{\mathrm{FWHM}}=\Gamma, \qquad \Delta\nu_{\mathrm{FWHM}}=\frac{\Gamma}{2\pi}.

This relation is convention-dependent once extra dephasing, power broadening, or a different definition of Γ\Gamma is introduced. A reliable report gives the decay law, the width definition, and the frequency unit rather than only a symbol.

The mapping

TE=EkBT_E=\frac{E}{k_{\mathrm B}}

answers: “What temperature has thermal energy kBTk_{\mathrm B}T equal to this energy scale?” It does not assert that a single photon, level splitting, trap depth, or recoil energy is itself a thermodynamic temperature.

Examples include:

  • a trap depth U0/kB=1 mKU_0/k_{\mathrm B}=1\ \mathrm{mK};
  • a recoil scale Er/kB=200 nKE_r/k_{\mathrm B}=200\ \mathrm{nK};
  • a hyperfine splitting expressed as an equivalent kelvin; and
  • a vibrational quantum compared with kBTk_{\mathrm B}T to estimate thermal occupation.

For a two-level energy gap ΔE>0\Delta E>0 in thermal equilibrium,

pepg=e−ΔE/(kBT).\frac{p_e}{p_g} =e^{-\Delta E/(k_{\mathrm B}T)}.

Here the ratio depends on both the gap-equivalent temperature TE=ΔE/kBT_E=\Delta E/k_{\mathrm B} and the actual ensemble temperature TT. Conflating them erases the statistical-mechanical content.

Negative binding energies require care. Converting E=−13.6 eVE=-13.6\ \mathrm{eV} to a negative kelvin is algebraically possible, but a thermal comparison usually uses the positive ionization energy ∣E∣/kB|E|/k_{\mathrm B}.

The Bohr and nuclear magnetons convert magnetic fields into electron-scale and nuclear-scale energies:

μB=eℏ2me,μN=eℏ2mp.\mu_{\mathrm B} =\frac{e\hbar}{2m_e}, \qquad \mu_{\mathrm N} =\frac{e\hbar}{2m_p}.

Useful frequency forms are

μBh=13.996 244 9171(44) GHz T−1,μNh=7.622 593 2188(24) MHz T−1.\begin{aligned} \frac{\mu_{\mathrm B}}{h} &=13.996\,244\,9171(44)\ \mathrm{GHz\,T^{-1}},\\ \frac{\mu_{\mathrm N}}{h} &=7.622\,593\,2188(24)\ \mathrm{MHz\,T^{-1}}. \end{aligned}

Since 1 G=10−4 T1\ \mathrm G=10^{-4}\ \mathrm T,

μBh=1.399 624 49171 MHz G−1.\frac{\mu_{\mathrm B}}{h} =1.399\,624\,49171\ \mathrm{MHz\,G^{-1}}.

For a weak-field hyperfine Zeeman shift,

ΔE=gFμBB ΔmF,\Delta E =g_F\mu_{\mathrm B}B\,\Delta m_F,

so the shift in hertz is

Δν=gFμBhB ΔmF.\Delta\nu =g_F\frac{\mu_{\mathrm B}}{h}B\,\Delta m_F.

The sign depends on gFg_F, the magnetic-field direction, and the definition of the magnetic quantum number. The magneton supplies a scale, not the full magnetic moment. Nuclear moments also include species-dependent nuclear gg factors and may be quoted with signs.

Molecular electric dipoles are commonly reported in debye. IUPAC defines the debye as a non-SI unit with

1 D≈3.335 64×10−30 C m.1\ \mathrm D \approx3.335\,64\times10^{-30}\ \mathrm{C\,m}.

The 2022 CODATA atomic unit of electric dipole moment is

ea0=8.478 353 6198(13)×10−30 C m≈2.54175 D.ea_0 =8.478\,353\,6198(13)\times10^{-30}\ \mathrm{C\,m} \approx2.54175\ \mathrm D.

For a matrix element dd coupled to an electric field amplitude E\mathcal E,

Eint∼dE.E_{\mathrm{int}}\sim d\mathcal E.

A useful laboratory scale is

(1 D)(1 kV cm−1)h≈503.412 MHz.\frac{(1\ \mathrm D)(1\ \mathrm{kV\,cm^{-1}})}{h} \approx503.412\ \mathrm{MHz}.

This is a scale estimate, not a promise of a linear Stark shift. A parity eigenstate has no first-order diagonal electric dipole unless degeneracy, state mixing, orientation, or another symmetry-breaking mechanism permits it. For an optical transition, the relevant dd is a transition matrix element and field conventions may distinguish peak, root-mean-square, and complex amplitudes.

For vacuum wavelength in nanometres,

ν [THz]=299 792.458λ0 [nm],E [eV]=1 239.841 984 332…λ0 [nm],ν~ [cm−1]=107λ0 [nm].\begin{aligned} \nu\,[\mathrm{THz}] &=\frac{299\,792.458} {\lambda_0\,[\mathrm{nm}]},\\ E\,[\mathrm{eV}] &=\frac{1\,239.841\,984\,332\ldots} {\lambda_0\,[\mathrm{nm}]},\\ \tilde{\nu}\,[\mathrm{cm^{-1}}] &=\frac{10^7} {\lambda_0\,[\mathrm{nm}]}. \end{aligned}

These are compact forms of E=hc/λ0E=hc/\lambda_0, not independent empirical rules. Keeping the wavelength unit in the denominator is safer than memorizing a bare value such as “1240.”

For spectroscopy, frequency is usually the cleaner invariant quantity. Wavelength becomes nonlinear under uncertainty propagation:

λ0=cν,δλ0λ0≈−δνν\lambda_0=\frac{c}{\nu}, \qquad \frac{\delta\lambda_0}{\lambda_0} \approx-\frac{\delta\nu}{\nu}

for small changes. The minus sign says that a higher frequency has a shorter wavelength.

The Rydberg constant R∞R_\infty is an infinite-nuclear-mass quantity. At the leading nonrelativistic level for a nucleus of mass MM, replace mem_e by the reduced mass

μ=meMme+M.\mu =\frac{m_eM}{m_e+M}.

The corresponding scale is

RM=R∞μme=R∞1+me/M.R_M =R_\infty\frac{\mu}{m_e} =\frac{R_\infty}{1+m_e/M}.

Expanding for me/M≪1m_e/M\ll1 gives

RM≈R∞(1−meM).R_M \approx R_\infty \left(1-\frac{m_e}{M}\right).

This leading correction explains isotope-dependent shifts in simple hydrogenic reasoning, but precision predictions require recoil, nuclear-size, relativistic, radiative, and structure corrections. Do not use reduced-mass scaling as a substitute for a precision theory model.

Take a vacuum wavelength λ0=780 nm\lambda_0=780\ \mathrm{nm}. The cyclic frequency is

ν=cλ0=3.84349×1014 Hz=384.349 THz.\nu =\frac{c}{\lambda_0} =3.84349\times10^{14}\ \mathrm{Hz} =384.349\ \mathrm{THz}.

The photon energy is

E=hν=2.54672×10−19 J=1.58954 eV.E =h\nu =2.54672\times10^{-19}\ \mathrm J =1.58954\ \mathrm{eV}.

The vacuum wavenumber and energy-equivalent temperature are

ν~=12 820.5 cm−1,EkB=18 445.9 K.\tilde{\nu} =12\,820.5\ \mathrm{cm^{-1}}, \qquad \frac{E}{k_{\mathrm B}} =18\,445.9\ \mathrm K.

The last number does not mean a 780 nm laser beam has a temperature of 18 446 K18\,446\ \mathrm K. It states the single-photon energy in kelvin units.

The SI fixes the unperturbed ground-state hyperfine transition frequency of cesium-133 to

ΔνCs=9 192 631 770 Hz.\Delta\nu_{\mathrm{Cs}} =9\,192\,631\,770\ \mathrm{Hz}.

Its energy is

ΔE=hΔνCs=6.091 102 297 113 866 55×10−24 J.\Delta E =h\Delta\nu_{\mathrm{Cs}} =6.091\,102\,297\,113\,866\,55 \times10^{-24}\ \mathrm J.

Equivalent forms are

ΔE=38.0177 μeV,ΔEkB=0.441177 K,ΔEhc=0.306633 cm−1.\begin{aligned} \Delta E &=38.0177\ \mathrm{\mu eV},\\ \frac{\Delta E}{k_{\mathrm B}} &=0.441177\ \mathrm K,\\ \frac{\Delta E}{hc} &=0.306633\ \mathrm{cm^{-1}}. \end{aligned}

The frequency is exact as part of the SI definition. The statement does not say that every realized cesium clock is exact; real clocks carry statistical and systematic uncertainty.

Suppose a resonant drive is reported as

Ω2π=10 MHz.\frac{\Omega}{2\pi}=10\ \mathrm{MHz}.

Then

Ω=2π×107 rad s−1,\Omega =2\pi\times10^7\ \mathrm{rad\,s^{-1}},

and the resonant π\pi-pulse duration is

tπ=πΩ=50 ns.t_\pi =\frac{\pi}{\Omega} =50\ \mathrm{ns}.

Reading “10 MHz10\ \mathrm{MHz}” as Ω=107 rad s−1\Omega=10^7\ \mathrm{rad\,s^{-1}} would instead give tπ≈314 nst_\pi\approx314\ \mathrm{ns}. The physics did not change; the unstated convention did.

For gF=1/2g_F=1/2, ΔmF=1\Delta m_F=1, and B=100 μTB=100\ \mathrm{\mu T},

Δν=12(13.9962 GHz T−1)(10−4 T)≈699.8 kHz.\Delta\nu =\frac12 \left(13.9962\ \mathrm{GHz\,T^{-1}}\right) \left(10^{-4}\ \mathrm T\right) \approx699.8\ \mathrm{kHz}.

This is a weak-field linear estimate. Near hyperfine avoided crossings or in the Paschen–Back regime, diagonalize the appropriate Hamiltonian rather than extrapolate the linear formula.

For a reliable conversion:

  1. Identify the physical quantity, not only its dimensions.
  2. Write the source value with its unit.
  3. Choose one bridge equation from the master identity.
  4. Carry the unit algebra through the calculation.
  5. State whether a frequency is cyclic or angular.
  6. State vacuum or medium for wavelength and wavenumber.
  7. Round only after the conversion.
  8. Preserve the source uncertainty and correlations when they matter.

For example, converting a wavenumber ν~=125 cm−1\tilde{\nu}=125\ \mathrm{cm^{-1}} to energy should begin with

E=hcν~,E=hc\tilde{\nu},

and explicitly replace

125 cm−1=12 500 m−1.125\ \mathrm{cm^{-1}} =12\,500\ \mathrm{m^{-1}}.

Writing the factor of 100 makes the unit conversion visible and prevents a two-order-of-magnitude error.

Conversion does not create information. If a measured line is 384.230(5) THz384.230(5)\ \mathrm{THz}, reporting a wavelength with fifteen digits is misleading even though a calculator can produce them.

For y=y(x)y=y(x) and a small standard uncertainty u(x)u(x),

u(y)≈∣dydx∣u(x).u(y) \approx \left|\frac{dy}{dx}\right|u(x).

Thus for λ=c/ν\lambda=c/\nu,

u(λ)≈cν2u(ν).u(\lambda) \approx \frac{c}{\nu^2}u(\nu).

If several measured constants enter, use their covariance matrix:

u2(y)=∑i,j∂y∂xi∂y∂xjcov⁡(xi,xj).u^2(y) = \sum_{i,j} \frac{\partial y}{\partial x_i} \frac{\partial y}{\partial x_j} \operatorname{cov}(x_i,x_j).

CODATA values are correlated because they come from a joint least-squares adjustment. Treating them as independent can overstate or understate a precision uncertainty. For routine AMO scale estimates, rounded values are appropriate. For precision metrology, retrieve the current recommended values, uncertainties, and correlation coefficients from the official database.

A minimum numerical report should identify:

  • the constant set, such as “2022 CODATA”;
  • the frequency convention;
  • the wavelength medium;
  • the quoted uncertainty type;
  • the number of significant digits justified by the input; and
  • any atomic-unit, Gaussian-unit, or SI convention used in the source model.

Treating hertz and radians per second as interchangeable

Section titled “Treating hertz and radians per second as interchangeable”

Their dimensions can both be reduced to inverse seconds, but their numerical values differ by 2π2\pi. Keep Hz\mathrm{Hz} with hh and rad s−1\mathrm{rad\,s^{-1}} with ℏ\hbar.

ν~=1/λ0\tilde{\nu}=1/\lambda_0, whereas k=2π/λ0k=2\pi/\lambda_0. A quoted 10 000 cm−110\,000\ \mathrm{cm^{-1}} is normally a spectroscopic wavenumber.

The factor

1 cm−1=100 m−11\ \mathrm{cm^{-1}}=100\ \mathrm{m^{-1}}

must appear before using SI hh and cc.

Confusing the Rydberg constant and Rydberg energy

Section titled “Confusing the Rydberg constant and Rydberg energy”

R∞R_\infty has units of inverse length. The Rydberg energy is hcR∞hcR_\infty, and the Hartree energy is 2hcR∞2hcR_\infty.

Treating an equivalent kelvin as a sample temperature

Section titled “Treating an equivalent kelvin as a sample temperature”

E/kBE/k_{\mathrm B} is a scale comparison. Thermodynamic temperature requires an ensemble and an operational or statistical definition.

Electron magnetic scales are usually set by μB\mu_{\mathrm B}; nuclear magnetic scales are usually set by μN\mu_{\mathrm N} multiplied by a nuclear gg factor. The two magnetons differ by roughly the proton-to-electron mass ratio.

Ignoring the sign of charge or magnetic moment

Section titled “Ignoring the sign of charge or magnetic moment”

ee is a positive magnitude, but the electron charge and electron magnetic moment carry signs. State whether a formula uses signed moments or positive scales.

1 eV=1.602 176 634×10−19 J1\ \mathrm{eV}=1.602\,176\,634\times10^{-19}\ \mathrm J is exact in the current SI. A truncated decimal for ℏ\hbar is also derived from exact hh. By contrast, mem_e and α\alpha have measurement uncertainty.

After the 2019 SI revision, μ0\mu_0 and ϵ0\epsilon_0 are not exact. Old references that set μ0=4π×10−7 N A−2\mu_0=4\pi\times10^{-7}\ \mathrm{N\,A^{-2}} exactly use the pre-2019 SI.

At precision accuracy, a wavelength without a medium convention is underspecified. Prefer frequency when comparing results across environments.

Starting from E=hνE=h\nu and the definitions ω=2πν\omega=2\pi\nu, λ0=c/ν\lambda_0=c/\nu, and ν~=1/λ0\tilde{\nu}=1/\lambda_0, derive

E=ℏω=hcν~.E=\hbar\omega=hc\tilde{\nu}.

Explain why k=2πν~k=2\pi\tilde{\nu} does not introduce a contradiction.

Solution

Because ℏ=h/(2π)\hbar=h/(2\pi) and ω=2πν\omega=2\pi\nu,

ℏω=h2π(2πν)=hν=E.\hbar\omega =\frac{h}{2\pi}(2\pi\nu) =h\nu =E.

The vacuum wavelength relation gives

ν=cλ0,\nu=\frac{c}{\lambda_0},

so

E=hcλ0=hcν~.E =h\frac{c}{\lambda_0} =hc\tilde{\nu}.

The wavevector magnitude is k=2π/λ0=2πν~k=2\pi/\lambda_0=2\pi\tilde{\nu}, so the same energy can also be written

E=ℏck.E =\hbar ck.

The factors of 2π2\pi move together: hh pairs with ν~\tilde{\nu}, while ℏ\hbar pairs with kk.

Treat 589 nm589\ \mathrm{nm} as a vacuum wavelength. Convert it to terahertz, electronvolts, inverse centimetres, and energy-equivalent kelvin. Keep four significant figures.

Solution

The frequency is

ν=299 792.458589 THz=508.9855 THz.\nu =\frac{299\,792.458} {589}\ \mathrm{THz} =508.9855\ \mathrm{THz}.

The photon energy is

E=1 239.841984589 eV=2.104995 eV.E =\frac{1\,239.841984}{589}\ \mathrm{eV} =2.104995\ \mathrm{eV}.

The wavenumber is

ν~=107589 cm−1=16 977.93 cm−1,\tilde{\nu} =\frac{10^7}{589}\ \mathrm{cm^{-1}} =16\,977.93\ \mathrm{cm^{-1}},

and

TE=EkB=24 427.45 K.T_E =\frac{E}{k_{\mathrm B}} =24\,427.45\ \mathrm K.

To four significant figures:

509.0 THz,2.105 eV,1.698×104 cm−1,2.443×104 K.509.0\ \mathrm{THz}, \quad 2.105\ \mathrm{eV}, \quad 1.698\times10^4\ \mathrm{cm^{-1}}, \quad 2.443\times10^4\ \mathrm K.

Derive the frequency corresponding to 1 cm−11\ \mathrm{cm^{-1}} without using the conversion table.

Solution

Convert the inverse length first:

1 cm−1=100 m−1.1\ \mathrm{cm^{-1}} =100\ \mathrm{m^{-1}}.

Since ν=cν~\nu=c\tilde{\nu},

ν=(299 792 458 m s−1)(100 m−1).\nu = \left(299\,792\,458\ \mathrm{m\,s^{-1}}\right) \left(100\ \mathrm{m^{-1}}\right).

Therefore

ν=2.997 924 58×1010 Hz=29.979 2458 GHz.\nu =2.997\,924\,58\times10^{10}\ \mathrm{Hz} =29.979\,2458\ \mathrm{GHz}.

The result is exact because cc and the centimetre-to-metre relation are exact.

A laboratory note states “Rabi frequency 5 MHz5\ \mathrm{MHz}.” Compute the π\pi-pulse time under each of these interpretations:

  1. Ω/(2π)=5 MHz\Omega/(2\pi)=5\ \mathrm{MHz};
  2. Ω=5×106 rad s−1\Omega=5\times10^6\ \mathrm{rad\,s^{-1}}.

What should the note have written?

Solution

For a resonant two-level system,

tπ=πΩ.t_\pi=\frac{\pi}{\Omega}.

Under the first interpretation,

Ω=2π(5×106) rad s−1,\Omega =2\pi(5\times10^6)\ \mathrm{rad\,s^{-1}},

so

tπ=12(5×106)=100 ns.t_\pi =\frac{1}{2(5\times10^6)} =100\ \mathrm{ns}.

Under the second interpretation,

tπ=π5×106=0.6283 μs.t_\pi =\frac{\pi}{5\times10^6} =0.6283\ \mathrm{\mu s}.

The answers differ by 2π2\pi. The note should have written either Ω/(2π)=5 MHz\Omega/(2\pi)=5\ \mathrm{MHz} or Ω=5 Mrad s−1\Omega=5\ \mathrm{Mrad\,s^{-1}}.

Estimate the cyclic-frequency shift for gF=1/2g_F=1/2, ΔmF=1\Delta m_F=1, and B=100 μTB=100\ \mathrm{\mu T}. Use μB/h=13.9962 GHz T−1\mu_{\mathrm B}/h=13.9962\ \mathrm{GHz\,T^{-1}}.

Solution

The shift is

Δν=gFμBhBΔmF.\Delta\nu =g_F\frac{\mu_{\mathrm B}}{h}B\Delta m_F.

Since 100 μT=10−4 T100\ \mathrm{\mu T}=10^{-4}\ \mathrm T,

Δν=12(13.9962×109 Hz T−1)(10−4 T)=6.9981×105 Hz.\begin{aligned} \Delta\nu &=\frac12 \left(13.9962\times10^9\ \mathrm{Hz\,T^{-1}}\right) \left(10^{-4}\ \mathrm T\right)\\ &=6.9981\times10^5\ \mathrm{Hz}. \end{aligned}

Thus

Δν≈699.8 kHz.\Delta\nu\approx699.8\ \mathrm{kHz}.

Find the frequency scale dE/hd\mathcal E/h for d=2.0 Dd=2.0\ \mathrm D and E=5.0 kV cm−1\mathcal E=5.0\ \mathrm{kV\,cm^{-1}}. State one reason this need not equal an observed first-order Stark shift.

Solution

Using

(1 D)(1 kV cm−1)h≈503.412 MHz,\frac{(1\ \mathrm D)(1\ \mathrm{kV\,cm^{-1}})}{h} \approx503.412\ \mathrm{MHz},

gives

dEh≈(2.0)(5.0)(503.412 MHz)=5.034 GHz.\frac{d\mathcal E}{h} \approx (2.0)(5.0)(503.412\ \mathrm{MHz}) =5.034\ \mathrm{GHz}.

This is the bare interaction scale. A parity eigenstate can have zero first-order diagonal dipole moment; rotational averaging, matrix-element geometry, degeneracy, state mixing, and field polarization can all modify the observed shift.

Classify each statement as correct or incorrect.

  1. 1 eV1\ \mathrm{eV} in joules has experimental uncertainty.
  2. The displayed decimal for ℏ\hbar may be truncated even though ℏ\hbar is derived exactly from hh.
  3. μ0=4π×10−7 N A−2\mu_0=4\pi\times10^{-7}\ \mathrm{N\,A^{-2}} is exact in the current SI.
  4. A CODATA parenthesis such as (11)(11) marks uncertainty in the final digits.
Solution
  1. Incorrect. The elementary charge is fixed exactly, so 1 eV=1.602 176 634×10−19 J1\ \mathrm{eV}=1.602\,176\,634\times10^{-19}\ \mathrm J is exact.
  2. Correct. ℏ=h/(2π)\hbar=h/(2\pi) is derived exact, but its decimal expansion is nonterminating.
  3. Incorrect. Since the 2019 SI revision, μ0\mu_0 inherits uncertainty through the measured fine-structure constant.
  4. Correct. For a measured CODATA value, parenthetical digits give the one-standard-deviation uncertainty in the corresponding final digits.

Exercise 8: Repair an underspecified result

Section titled “Exercise 8: Repair an underspecified result”

A report says:

The linewidth is 6.1 MHz, the transition wavelength is 780.24 nm, and the Rabi frequency is 10 MHz.

List at least four missing convention or uncertainty statements needed for a reproducible precision comparison.

Solution

A defensible report should state at least:

  • whether the linewidth is a full width or half width;
  • whether the linewidth is in cyclic frequency or angular frequency;
  • the fitted line-shape model and whether power or inhomogeneous broadening is included;
  • whether the wavelength is in vacuum or in a specified medium;
  • the uncertainty and calibration basis of the wavelength or frequency;
  • whether the Rabi number means Ω/(2π)=10 MHz\Omega/(2\pi)=10\ \mathrm{MHz} or an angular frequency of 10 Mrad s−110\ \mathrm{Mrad\,s^{-1}};
  • whether the field amplitude is peak, root-mean-square, or a complex amplitude; and
  • which transition, polarization, magnetic sublevel, and detuning convention were used.

The original numbers may be useful estimates, but they are not yet a reproducible precision statement.

  • Reference and Data is the task-oriented gateway to AMO lookup pages and source-provenance rules.
  • Spectroscopy Nomenclature distinguishes vacuum and medium wavelength, ordinary and angular frequency, spectroscopic wavenumber, and coordinate-density Jacobians.
  • AMO Atomic Units gives the quantity-specific Hartree multipliers, Rydberg diagnostics, and dimensional restoration rules.
  • Units and Constants gives the global reporting policy.
  • Constants is the compact site-wide numerical table.
  • Units compares SI, atomic, natural, and common quantum-mechanical units.
  • Atomic Units and Scales derives Hartree units and their physical hierarchy.
  • Fundamental Constants develops adjustment, correlations, and precision determinations.
  • Line Shapes and Broadening defines spectral widths and broadening mechanisms.
  • Rabi Oscillations fixes the drive-amplitude and angular-frequency conventions used in coherent control.
  • Atomic Units is the canonical atomic-unit translator.
  • Hbar Conventions explains how to restore ℏ\hbar after a natural-unit calculation.
  1. Bureau International des Poids et Mesures, The International System of Units (SI), 9th ed., version 4.01 (2026), doi:10.59161/AUEZ1291.
  2. E. Tiesinga, P. J. Mohr, D. B. Newell, and B. N. Taylor, “CODATA Recommended Values of the Fundamental Physical Constants: 2022,” Journal of Physical and Chemical Reference Data 54, 033105 (2025), doi:10.1063/5.0279860.
  3. NIST Physical Measurement Laboratory, Fundamental Physical Constants, 2022 CODATA web version 9.0, updated May 2024.
  4. NIST Physical Measurement Laboratory, Conversion Factors for Energy Equivalents, based on the 2022 CODATA adjustment.
  5. National Institute of Standards and Technology, The International System of Units: NIST Special Publication 330, section 2, “SI units.”
  6. International Union of Pure and Applied Chemistry, “Wavenumber,” Compendium of Chemical Terminology, 5th ed. (2025), doi:10.1351/goldbook.W06664.
  7. International Union of Pure and Applied Chemistry, “Frequency,” Compendium of Chemical Terminology, 5th ed. (2025), doi:10.1351/goldbook.FT07383.
  8. International Union of Pure and Applied Chemistry, “Debye,” Compendium of Chemical Terminology, 5th ed. (2025), doi:10.1351/goldbook.D01533.