ABSTRACT
We employ fluorescence correlation spectroscopy (FCS) and coarse-grained molecular dynamics simulations to study the mobility of tracers in polymer solutions. Excluded volume interactions result in crowding-induced slowdown, depending only on the polymer concentration. With specific tracer-polymer attractions, the tracer is slowed down at much lower concentrations, and a second diffusion component appears that is sensitive to the polymer chain length. The two components can be resolved by FCS, only if the distance traveled by the tracer in the polymer-bound state is greater than the FCS focal spot size. The tracer dynamics can be used as a sensitive probe of the nature and strength of interactions, which-despite their local character-emphasize the role of chain connectivity.
ABSTRACT
We performed fluorescence correlation spectroscopy measurements to assess the long-time self-diffusion of a variety of spherical tracer particles in periodic porous nanostructures. Inverse opal structures with variable cavity sizes and openings in the nanometer domain were employed as the model system. We obtained both the exponent of the scaling relation between mean-square displacement and time and the slow-down factors due to the periodic confinement for a number of particle sizes and confining characteristics. In addition, we carried out Brownian dynamics simulations to model the experimental conditions. Good agreement between experimental and simulation results has been obtained regarding the slow-down factor. Fickian diffusion is predicted and seen in almost all experimental systems, while apparent non-Fickian exponents that show up for two strongly confined systems are attributed to polydispersity of the cavity openings. The utility of confining periodic porous nanostructures holds promise toward understanding of constrained diffusion with a wide range of applications ranging from water purification and drug delivery to tissue engineering.
