Abstract
Multiplex coherent anti-Stokes Raman scattering correlation spectroscopy (CARS-CS) is shown as a label-free, chemically specific approach for monitoring the molecular mobility of particles in solution and at interfaces on the millisecond time scale. The CARS spectral range afforded by broadband excitation facilitates a quantitative measurement for the number of particles in the focal volume, whereas the autocorrelation of spectral data elucidates dynamic events, such as diffusion. The measured diffusion coefficients for polymer beads ranging from 100 nm to 1.1 μm in diameter are on the order of 10(-8)-10(-9) cm(2)/s, in good agreement with predicted Stokes-Einstein values. Diffusion at different interfaces shows particles are fastest in bulk medium, marginally slower at the liquid/glass interface, and 1.5-2 times slower rate at the air/liquid interface. Multivariate curve resolution analysis of distinct spectral features in multiplex CARS measurement distinguishes different composition lipid vesicles in a mixture diffusing through the focal volume. The observed diffusion is consistent with results obtained from single particle tracking experiments. This work demonstrates the utility of multiplex CARS correlation spectroscopy for monitoring particle diffusion from different chemical species across diverse interfaces.