Cumulants DLS


DLS analysis by the method of Cumulants.



This model is in part provided to illustrate the utility of SasView as a fitting program for the analysis of input data that is NOT $I(q)$ vs $q$. But at the same time it usefully provides a basic means of analysing Dynamic Light Scattering (DLS) data using the Method of Cumulants (Koppel, 1972).

Note: The Method of Cumulants is only valid if the particle size distribution is monomodal. However, the size distribution can be polydisperse.

Input Data

The input data can be in any data format recognised by the SasView data loader, though a format containing delimited two-column ASCII text will probably be the most convenient.

SasView will look for the first pair of numerical values in the file, so it is permissible to prefix the data with some lines of metadata and/or column headers, but none of these will be imported. If the file contains multiple data blocks it is likely that only the first one will be imported, so it is important that the data you want to fit is the first data block in the file. This reasonable degree of flexibility means that in some instances data files output by commercial correlators can be read by SasView 'as is', without any need for reformatting.

For example, this is a text format output by an LSi Correlator (see :

03/08/2020 17:30 PM
Pseudo Cross Correlation
Scattering angle: 110.0
Duration (s): 60
Wavelength (nm): 642.0
Refractive index: 1.330
Viscosity (mPas): 0.854
Temperature (K): 309.0
Laser intensity (mW): 0.0
Average Count rate A (kHz): 19388.1
Average Count rate B (kHz): 19388.1
Intercept: 1.0000
Cumulant 1st -Inf
Cumulant 2nd -Inf NaN
Cumulant 3rd -Inf NaN

Lag time (s) g2-1
0.000000e+00 2.153341e+02
1.250000e-08 -1.000000e+00
2.500000e-08 1.897621e-02
3.750000e-08 1.454616e+00
5.000000e-08 1.040391e+00
6.250000e-08 9.113997e-01
7.500000e-08 8.547216e-01
8.750000e-08 8.269044e-01
1.000000e-07 7.905431e-01
1.125000e-07 7.863978e-01
1.250000e-07 7.645010e-01
1.375000e-07 7.728501e-01
1.500000e-07 7.646473e-01
1.625000e-07 7.516946e-01
1.750000e-07 7.575662e-01
1.875000e-07 7.556643e-01
2.000000e-07 7.547962e-01
5.033165e+01 -5.472073e-03

Count Rate History (KHz) CR CHA / CR CHB
0.000000 18560.000000 18560.000000
59.926118 16078.000000 16078.000000

In this example, SasView ignores all the metadata preceding the first (two-column) data block, the correlation function, and ignores everything after the two-column data block.

Whatever the file format it is imperative that the correct data is placed in these the two columns:

Column 1: what would normally be $q$: Correlator time or $\tau$ (in seconds)

Column 2: what would normally be $I(q)$: Normalised Intensity Autocorrelation Function, $G2(\tau)$

Method of Analysis

For a monomodal dispersion of MONODISPERSE scatterers

$$G2(\tau) = \text{A} \cdot exp(-2 \Gamma \tau) + \text{background}$$

where $\Gamma = D \cdot q^2$ is the decay rate, $D$ is the mutual diffusion coefficient and $q$ is the scattering vector.

For a monomodal dispersion of POLYDISPERSE scatterers Koppel showed

$$G2(\tau) = \text{A} \cdot exp(-2 \Gamma_1 \tau + \Gamma_2 \tau^2 - (1/3) \Gamma_3 \tau^3 + ...) + \text{background}$$

where each $\Gamma$ is a cumulant of the distribution of decay rates arising from the different sized scatterers. However, this function is unstable. A more stable function is (Pusey et al, 1974; Frisken, 2001; Mailer et al, 2015)

$$G2(\tau) = \text{A} \cdot exp(-2 \Gamma_1 \tau) \cdot (1 + (1/2) \Gamma_2 \tau^2 - (1/6) \Gamma_3 \tau^3 + ...)^2 + \text{background}$$

Here $\Gamma_1$ is now the AVERAGE decay rate (representing a weighted average of the different diffusion coefficients) and $\Gamma_2$ is related to the relative polydispersity index, $PDI = \Gamma_2 / \Gamma_1^2$.

Note: This PDI must not be confused with dispersity indicies measured by static light-scattering (where it is the ratio of the weight-average molar mass to the number-average molar mass, Mw/Mn), viscometry, etc. The PDI from DLS has a range of 0-1 where, in theory, a value of 0 represents a monodisperse system. In the case of Mw/Mn dispersity, a monodisperse system is represented by a value of 1!

In practical terms, a PDI of <0.05 is indicative of a monodisperse system. PDI's of 0.1 to 0.7 represent systems that are nearly monodisperse, whereas a PDI >0.7 suggests significant polydispersity (Stetefeld et al, 2016). For more information, also see the section Polydispersity & Orientational Distributions in the SasView User Documentation.

The third cumulant is related to the SKEWNESS of the decay rate distribution ($\Gamma_3 / \Gamma_2^{3/2}$) and the fourth cumulant (not implemented in this model) gives the KURTOSIS ($\Gamma_4 / \Gamma_2^2$). Further cumulants are rarely, if ever, used.

FORMULA 2 is used by default in this model, but both formulae are provided below. Simply comment/uncomment whichever is required.

Mutual Diffusion Coefficient & Size

The usefulness of $D$ is that it is related to the size and shape of the scatterers through

$$D = \frac{k_B T}{f}$$

where $k_B$ is the Boltzmann Constant, $T$ is the absolute temperature, and $f$ is a quantity called the Friction Factor. This relationship is valid so long as the system is dilute.

In the case of spherical scatterers Stoke's Law gives $f = 6 \pi \eta R$ where $\eta$ is the viscosity of the dispersion medium and $R$ is the radius of the spheres. Combining these two functions then leads to the well-known Stokes-Einstein relation

$$D = \frac{k_B T}{6 \pi \eta R}$$

It is this function that this model uses to compute a radius. If the system is polydisperse then $R$ is a z-average value.

If the scatterers are not spherical then either $f$ or $R$ must be adjusted accordingly.

Using this Model

The parameters $angle$, $temperature$, $viscosity$, $ref$_$index$, and $wavelength$ are for defining the experimental conditions to enable the correct calculation of $R$. THEY MUST NOT BE FITTED! Do not tick their checkboxes.

The $scale$ parameter will be what many commercial DLS software packages refer to as the $Intercept$ of the correlation function. This must be between 0 and 1, but for the data to have any real meaning it should be between 0.6 and 1.

If the correlator has supplied its output as $G2(\tau)-1$ (as in the data file example above) then $background$ should be essentially zero.

Do not attempt to fit all of the tail of the correlation function. Use the min and max $q$-range for fitting boxes to limit the fit range to a sensible region of the correlation function. You only need to fit the decay and the start of the tail.

The best way to approach fitting the data is to gradually increase the number of cumulants being fitted. So, initially, set $pdi$ and $cumulant3$ to zero, and fit (check the boxes) the parameters $scale$, $background$ and $radius$. Then fit the $pdi$. Then (if required) fit $cumulant3$.

To view the fit it will probably be helpful to change the y-axis scale from the SasView default of log(y) to y. To do this, right-click on the graph. It is also possible to change the x and y axis labels from their SasView defaults of $q$ and $intensity$.


This model is inspired by a similar model in the SASfit model-fitting package (Kohlbrecher, 2020).

Also see the model cumulants in the SasView Marketplace.


1. D. E. Koppel. Analysis of macromolecular polydispersity in intensity correlation spectroscopy: The method of cumulants. The Journal of Chemical Physics, (1972), 57(11),
2. P. N. Pusey, D. E. Koppel, D. E. Schaefer, R. D. Camerini-Otero, and S. H. Koenig. Intensity fluctuation spectroscopy of laser light scattered by solutions of spherical viruses.
r17, q.beta., BSV, PM2, and t7. i. light-scattering technique. Biochemistry, (1974), 13(5), 952-960.
3. B. J. Frisken. Revisiting the method of cumulants for the analysis of dynamic light-scattering data. Applied Optics, (2001), 40(24), 4087.
4. A. G. Mailer, P. S. Clegg, and P. N. Pusey. Particle sizing by dynamic light scattering: nonlinear cumulant analysis. Journal of Physics: Condensed Matter, (2015), 27(14),
5. J. Stetefeld, S. A. McKenna1 & T. R. Patel. Dynamic light scattering: a practical guide and applications in biomedical sciences. Biophys Rev (2016), 8, 409-427.
6. J. Kohlbrecher. User guide for the SASfit software package. Chapter 13. June 2020.


The model has been tested by comparing its output to that from the commercial LSi correlator software using the same input data and range of $\tau$.

For a nominal 30 nm diameter PS latex standard:

LSi : intercept = 0.750, radius = 13.7 nm, width = 2.89 nm
SasView: intercept = 0.743, radius = 13.64 nm, pdi = 0.089

For a PNIPAM microgel:

LSi : intercept = 0.694, radius = 275 nm, width = 90.6 nm
SasView: intercept = 0.716, radius = 290.0 nm, pdi = 0.675

Both sets of fits reproduce the $intercept$ well, and recognise a big difference between the polydispersity of the samples, although it appears that as the polydispersity increases the reliability of the $radius$ parameter is called into question. However, visually, SasView appears to do a much better job of fitting the data than the commercial software. This may reflect the fact that SasView has much better optimisers.

Authorship History

Author: Steve King Date: 25/08/2020
Last Modified by: Date:
Last Reviewed by: Date:


Created By smk78
Uploaded Aug. 25, 2020, 8:02 p.m.
Category DLS
Score 0
Verified This model has not been verified by a member of the SasView team
In Library This model is not currently included in the SasView library. You must download the files and install it yourself.


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