RESUMEN
Molecular dynamics simulations are applied to investigate salt-free planar polyelectrolyte brushes under poor solvent conditions. Starting above the Θ-point with a homogeneous brush and then gradually reducing the temperature, the polymers initially display a lateral structure formation, forming vertical bundles of chains. A further reduction of the temperature (or solvent quality) leads to a vertical collapse of the brush. By varying the size and selectivity of the counterions, we show that lateral structure formation persists and therefore demonstrate that the entropy of counterions being the dominant factor for the formation of the bundle phase. By applying an external compression force on the brush we calculate the minimal work done on the polymer phase only and prove that the entropy gain of counterions in the bundle state, as compared to the homogeneously collapsed state at the same temperature, is responsible for the lateral microphase segregation. As a consequence, the observed lateral structure formation has to be regarded universal for osmotic polymer brushes below the Θ-point.
RESUMEN
Using nonequilibrium Brownian dynamics computer simulations, we have investigated the steady state statistics of a polymer chain under three different shear environments: (i) linear shear flow in the bulk (no interfaces), (ii) shear vorticity normal to the adsorbing interface, and (iii) shear gradient normal to the adsorbing interface. The statistical distribution of the chain end-to-end distance and its orientational angles are calculated within our computer simulations. Over a wide range of shear rates, this distribution can be mapped onto a simple theoretical finite-extensible-nonlinear-elastic dumbbell model with fitted anisotropic effective spring constants. The tails of the angular distribution functions are consistent with scaling predictions borrowed from the bulk dumbbell model. Finally, the frequency of the characteristic periodic tumbling motion has been investigated by simulation as well and was found to be sublinear with the shear rate for the three setups, which extends earlier results done in experiments and simulations for free and tethered polymer molecules without adsorption.
RESUMEN
Via computer simulations, we demonstrate how a densely grafted layer of polymers, a brush, could be turned into an efficient switch through chemical modification of some of its end monomers. In this way, a surface coating with reversibly switchable properties can be constructed. We analyze the fundamental physical principle behind its function, a recently discovered surface instability, and demonstrate that the combination of a high grafting density, an inflated end-group size, and a high degree of monodispersity is a condition for an optimal functionality of the switch.