The typical DDM data is a time sequence of microscope images acquired at some height within the sample. If the image intensity is locally proportional to the concentration of particles or molecules to be studied, each movie can be analyzed in the Fourier space to obtain information about the dynamics of concentration Fourier modes, independent on the fact that the particles/molecules can be individually optically resolved or not. After suitable calibration also information about the Fourier amplitude of the concentration modes can be extracted.
Applicability and working principle
The concentration-intensity proportionality is valid at least in two very important cases that distinguish two corresponding classes of DDM methods:
scattering-based DDM: where the image is the result of the superposition of the strong transmitted beam with the weakly scattered light from the particles. Typical cases where this condition can be obtained are bright field, phase contrast, polarized microscopes.
fluorescence-based DDM: where the image is the result of the incoherent addition of the intensity emitted by the particles microscopes
In both cases the convolution with the PSF in the real space corresponds to a simple product in the Fourier space, which guarantees that studying a given Fourier mode of the image intensity provides information about the corresponding Fourier mode of the concentration field. In contrast with particle tracking, there is no need of resolving the individual particles, which allows DDM to characterize the dynamics of particles or other moving entities whose size is much smaller than the wavelength of light. Still, the images are acquired in the real space, which provides several advantages with respect to traditional scattering methods.
Data analysis
DDM is based on an algorithm proposed in and, which is conveniently named Differential Dynamic Algorithm. DDA works by subtracting images acquired at different times and taking advantage that, as the delay between two subtracted images gets large, the energy content of the difference image increases correspondingly. A two-dimensional Fast Fourier Transform analysis of the difference images allows to quantify the growth of the signal contains for each wave vector and one can calculate the Fourier power spectrum of the difference images for different delays to obtain the so-called image structure function. Calculation shows that for both scattering- and fluorescence-based DDM where is the normalized intermediate scattering function that would be measured in a Dynamic Light Scattering experiment, the sample scattering intensity that would be measured in a Static Light Scattering experiment, a background term due to the noise along the detection chain a transfer function that depends on the microscope details. Equation shows that DDM can be used for DLS experiments, provided that a model for the normalized intermediate scattering function is available. For instance, in the case of Brownian motion one has where is the diffusion coefficient of the Brownian particles. If the transfer function is determined by calibrating the microscope with a suitable sample, DDM can be employed also for SLS experiments. Alternative algorithms for data analysis are suggested in.
Relationship with other imaging-based scattering methods
Scattering-based DDM belongs to the so-called near-field scattering family, a recently introduced family of imaging-based scattering methods. Near field is used here in a similar way to what is used for near field speckles i.e. as a particular case of Fresnel region as opposed to the far field or Fraunhofer region. The near field scattering family includes also quantitative shadowgraphy and Schlieren.
Applications of DDM
DDM was introduced in 2008 and it was applied for characterizing the dynamics of colloidal particles in Brownian motion. More recently it has been successfully applied also to the study of aggregation processes of colloidal nanoparticles, of bacterial motions and of the dynamics of anisotropic colloids.
