Plot of the centered Voigt profile for four cases. Each case has a full width at half-maximum of very nearly 3.6. The black and red profiles are the limiting cases of the Gaussian (γ =0) and the Lorentzian (σ =0) profiles respectively.
In spectroscopy, a Voigt profile results from the convolution of two broadening mechanisms, one of which alone would produce a Gaussian profile (usually, as a result of the Doppler broadening), and the other would produce a Lorentzian profile. Voigt profiles are common in many branches of spectroscopy and diffraction. Due to the expense of computing the Faddeeva function, the Voigt profile is sometimes approximated using a pseudo-Voigt profile.
since it is a convolution of normalized profiles. The Lorentzian profile has no moments (other than the zeroth), and so the moment-generating function for the Cauchy distribution is not defined. It follows that the Voigt profile will not have a moment-generating function either, but the characteristic function for the Cauchy distribution is well defined, as is the characteristic function for the normal distribution. The characteristic function for the (centered) Voigt profile will then be the product of the two:
Since normal distributions and Cauchy distributions are stable distributions, they are each closed under convolution (up to change of scale), and it follows that the Voigt distributions are also closed under convolution.
where is a hypergeometric function. In order for the function to approach zero as x approaches negative infinity (as the CDF must do), an integration constant of 1/2 must be added. This gives for the CDF of Voigt:
Using the definition above for and , the first and second derivatives can be expressed in terms of the Faddeeva function as
and
respectively.
Often, one or multiple Voigt profiles and/or their respective derivatives need to be fitted to a measured signal by means of non-linear least squares, e.g., in spectroscopy. Then, further partial derivatives can be utilised to accelerate computations. Instead of approximating the Jacobian matrix with respect to the parameters , , and with the aid of finite differences, the corresponding analytical expressions can be applied. With and , these are given by:
for the original voigt profile ;
for the first order partial derivative ; and
for the second order partial derivative . Since and play a relatively similar role in the calculation of , their respective partial derivatives also look quite similar in terms of their structure, although they result in totally different derivative profiles. Indeed, the partial derivatives with respect to and show more similarity since both are width parameters. All these derivatives involve only simple operations (multiplications and additions) because the computationally expensive and are readily obtained when computing . Such a reuse of previous calculations allows for a derivation at minimum costs. This is not the case for finite difference gradient approximation as it requires the evaluation of for each gradient respectively.
The Tepper-García function, named after German-Mexican Astrophysicist Thor Tepper-García, is a combination of an exponential function and rational functions that approximates the line broadening function over a wide range of its parameters.[2]
It is obtained from a truncated power series expansion of the exact line broadening function.
In its most computationally efficient form, the Tepper-García function can be expressed as
where , , and .
Thus the line broadening function can be viewed, to first order, as a pure Gaussian function plus a correction factor that depends linearly on the microscopic properties of the absorbing medium (encoded in ); however, as a result of the early truncation in the series expansion, the error in the approximation is still of order , i.e. . This approximation has a relative accuracy of
over the full wavelength range of , provided that .
In addition to its high accuracy, the function is easy to implement as well as computationally fast. It is widely used in the field of quasar absorption line analysis.[3]
There are several possible choices for the parameter.[4][5][6][7] A simple formula, accurate to 1%, is[8][9]
where now, is a function of Lorentz (), Gaussian () and total () Full width at half maximum (FWHM) parameters. The total FWHM () parameter is described by:
The full width at half maximum (FWHM) of the Voigt profile can be found from the
widths of the associated Gaussian and Lorentzian widths. The FWHM of the Gaussian profile
is
The FWHM of the Lorentzian profile is
An approximate relation (accurate to within about 1.2%) between the widths of the Voigt, Gaussian, and Lorentzian profiles is:[10]
By construction, this expression is exact for a pure Gaussian or Lorentzian.
A better approximation with an accuracy of 0.02% is given by [11] (originally found by Kielkopf[12])
Again, this expression is exact for a pure Gaussian or Lorentzian.
In the same publication,[11] a slightly more precise (within 0.012%), yet significantly more complicated expression can be found.
The asymmetry pseudo-Voigt (Martinelli) function resembles a split normal distribution by having different widths on each side of the peak position. Mathematically this is expressed as:
with being the weight of the Lorentzian and the width being a split function (for and for ). In the limit , the Martinelli function returns to a symmetry pseudo Voigt function. The Martinelli function has been used to model elastic scattering on resonant inelastic X-ray scattering instruments.[13]
^Wertheim GK, Butler MA, West KW, Buchanan DN (1974). "Determination of the Gaussian and Lorentzian content of experimental line shapes". Review of Scientific Instruments. 45 (11): 1369–1371. Bibcode:1974RScI...45.1369W. doi:10.1063/1.1686503.
^Sánchez-Bajo, F.; F. L. Cumbrera (August 1997). "The Use of the Pseudo-Voigt Function in the Variance Method of X-ray Line-Broadening Analysis". Journal of Applied Crystallography. 30 (4): 427–430. Bibcode:1997JApCr..30..427S. doi:10.1107/S0021889896015464.
^Ida T, Ando M, Toraya H (2000). "Extended pseudo-Voigt function for approximating the Voigt profile". Journal of Applied Crystallography. 33 (6): 1311–1316. doi:10.1107/s0021889800010219. S2CID55372305.
^P. Thompson, D. E. Cox and J. B. Hastings (1987). "Rietveld refinement of Debye-Scherrer synchrotron X-ray data from Al2O3". Journal of Applied Crystallography. 20 (2): 79–83. Bibcode:1987JApCr..20...79T. doi:10.1107/S0021889887087090.
^John F. Kielkopf (1973), "New approximation to the Voigt function with applications to spectral-line profile analysis", Journal of the Optical Society of America, 63 (8): 987, Bibcode:1973JOSA...63..987K, doi:10.1364/JOSA.63.000987
^Martinelli, L.; Biało, I.; Hong, X.; Oppliger, J.; et al. (2024). "Decoupled static and dynamical charge correlations in La2−xSrxCuO4". arXiv:2406.15062 [cond-mat.str-el].
http://jugit.fz-juelich.de/mlz/libcerf, numeric C library for complex error functions, provides a function voigt(x, sigma, gamma) with approximately 13–14 digits precision.
The original article is : Voigt, Woldemar, 1912, ''Das Gesetz der Intensitätsverteilung innerhalb der Linien eines Gasspektrums'', Sitzungsbericht der Bayerischen Akademie der Wissenschaften, 25, 603 (see also: http://publikationen.badw.de/de/003395768)