Prof Ramin Golestanian

Abstract:

The effective elasticity of highly charged stiff polyelectrolytes is studied in the presence of counterions, with and without added salt. The rigid polymer conformations may become unstable due to an effective attraction induced by counterion density fluctuations. Instabilities at the longest, or intermediate length scales, may signal collapse to globule, or necklace states, respectively. In the presence of added salt, a generalized electrostatic persistence length is obtained, which has a nontrivial dependence on the Debye screening length. It is also found that the onset of conformational instability is a reentrant phenomenon as a function of polyelectrolyte length for the unscreened case, and the Debye length or salt concentration for the screened case. This may be relevant in understanding the experimentally observed reentrant condensation of DNA.

Abstract:

We study the effect of electrostatic interactions on the distribution function of the end-to-end distance of a single polyelectrolyte chain in the rod-like limit. The extent to which the radial distribution function of a polyelectrolyte is reproduced by that of a wormlike chain with an adjusted effective persistence length is investigated. Strong evidence is found for a universal scaling formula connecting the effective persistence length of a polyelectrolyte with the strength of the electrostatic interaction and the Debye screening length.

Abstract:

Dynamics of an array of line defects interacting with a background elastic medium is studied in the linear regime. It is shown that the inertial coupling between the defects and the ambient phonons leads to an anomalous response behavior for the deformation modes of a defect-lattice, in the form of anisotropic and anomalous mass and elastic constants, resonant dissipation through excitation of phonons, and instabilities. The case of a single fluctuating line defect is also studied, and it is shown that it could lead to formation of shock waves in the elastic medium for sufficiently high frequency deformation modes.

Abstract:

The conventional assumption that the self-diffusion coefficient of a small tracer can be obtained by a local and instantaneous application of Einstein's relation in a temperature field with spatial and temporal heterogeneity is revisited. It is shown that hydrodynamic fluctuations contribute to the self-diffusion tensor in a universal way, i.e. independent of the size and shape of the tracer. The hydrodynamic contribution is anisotropic--it reflects knowledge of the global anisotropy in the temperature profile, leading to anisotropic self-diffusion tensor for a spherical tracer. It is also retarded--it creates memory effects during the diffusion process due to hydrodynamic interactions.