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Using Brownian dynamics simulations, we study the effect of the charge ratio, the surfactant length, and the grafting density on the conformational behavior of the complex formed by the polyelectrolyte brush with oppositely charged surfactants. In our simulations, the polyelectrolyte chains and surfactants are represented by a coarse-grained bead-spring model, and the solvent is treated implicitly. It is found that varying the charge ratio induces different morphologies of surfactant aggregates adsorbed onto the brush. At high charge ratios, the density profiles of surfactant monomers indicate that surfactant aggregates exhibit a layer-by-layer arrangement. The surfactant length has a strong effect on the adsorption behavior of surfactants. The lengthening of surfactant leads to a collapsed brush configuration, but a reswelling of the brush with further increasing the surfactant length is observed. The collapse of the brush is attributed to the enhancement of surfactants binding to polyelectrolyte chains. The reswelling is due to an increase in the volume of adsorbed surfactant aggregates. At the largest grafting density investigated, enhanced excluded volume interactions limit the adsorption of surfactant within the polyelectrolyte brush. We also find that end monomers in polyelectrolyte chains exhibit a bimodal distribution in cases of large surfactant lengths and high charge ratios. [ABSTRACT FROM AUTHOR]

Abstract: The electrophoretical stretching of DNA in a hybrid microchannel is analyzed in this paper. The channel comprises a large insulating cylinder and a hyperbolic contraction that can cause the DNA deformation. Brownian dynamics simulation is used to characterize the dynamical stretching process of a long T4 DNA in hybrid microchannels. The computational results show us the larger average extension of DNA in cylinder-hybridized microchannels than that in the single microcontractions due to the prestretched effect of cylinder on DNA. Moreover, the location and the radius of the insulating cylinder in hybrid microchannels have great effects on the stretching behavior of DNA. [Copyright &y& Elsevier]

We investigate polyelectrolytes end-grafted on two apposing walls using molecular dynamics simulation techniques. Monovalent and trivalent counterions are explicitly treated. Under normal compression, the osmotic pressure is examined in detail by decomposing it into various virial terms. It has been found that at small wall separations the increase in the osmotic pressure can be ascribed to the increase in the short-range virial term. At large wall separations, a negative osmotic pressure is observed in trivalent systems. Moreover, we study the effect of lateral shear on the density profiles of monomers and counterions, the net charge distribution, the local pressure tensor, the degree of interpenetration and the friction coefficient. At large shear ratios, the electrostatic interactions are weakened at the interface between two brushes. It is worth noting that although the magnitudes of the normal and shear stress components for the trivalent case are significantly lesser than those for the monovalent case, the friction coefficient is larger in the trivalent systems. [ABSTRACT FROM AUTHOR]

We conducted coarse-grained molecular dynamics simulations to study the responsive behaviors of polyampholyte brushes (PABs) under external electric fields. The effects of charge sequence, chain rigidity and electric field strength on the conformational transition and local structures of grafted chains were addressed systematically. Without electric field, the calculations indicate that the thickness of the PABs is smaller compared to polyelectrolyte brushes (PEBs). The presence of electric field leads to inconsistency of densities between negatively and positively charged monomers except for the alternating brush. Counterions from the PABs can diffuse inside or outside the brush. Unlike the PABs, to separate the polyelectrolytes and their counterions the electric field needs to overcome the osmotic pressure of counterions. The critical field which induces the extension of the flexible PABs is much larger than the PEBs. Meanwhile, it was also found that the critical field which induces the collapse of the PABs decreases as the block length increases. In the limit of strong field studied, the chains with longer blocks are in a local extended state. For diblock brushes, once oppositely charged blocks in a single chain are separated, the chain will become straighter due to strong electrostatic repulsion in intrablock. [ABSTRACT FROM AUTHOR]

We report an all-atom molecular dynamics study of the structures and dynamics of salty water droplets on a silicon surface under the influence of applied electric field. Our simulation results support ion-specific effects on the elongation dynamics of salty nanodroplets, induced by the field. This feature has not been explored up to now in monovalent salts. Nevertheless, the importance of ion-specific effects is widely confirmed in biological and colloidal systems. In particular, the increase of salt concentration enhances the effect of the nature of ions on the wetting properties of droplets. In the presence of electric field (0.05 V Å-1), a complete spreading is implemented in a short time for different droplets at a concentration of 1 M, and the droplet morphology is stable, observed at long time scales. However, a higher salt concentration of 4 M considerably suppresses the spreading process owing to the increase of surface tension. It was found that the NaCl droplet shows deformation oscillations along the external field, but cannot fully wet the substrate surface. By contrast, the CsCl droplet reaches complete elongation rapidly and adopts a steady strip shape. The KCl droplet undergoes frequent transitions between breakup and connection. Additionally, the droplets can be elongated only when the electric field strength exceeds a threshold value. The dipole orientation of interfacial water and the ionic diffusion exhibit ion-specific dependences, but the hydrogen bond network is scarcely disturbed, excluding a concentration-dependent effect. [ABSTRACT FROM AUTHOR]

In this paper, the self-assembly process of diblock copolymers confined in multi-walled cylindrical nanotubes is systematically investigated using a molecular dynamics (MD) method. The dependence of resultant morphologies on the degree of confinement and on the interaction strength between nanotubes and copolymers is studied comprehensively. When the wall surfaces are not preferential, results indicate that geometric confinement significantly influences copolymer conformations. In addition, the thickness of the helical lamellar structure increases with interaction strength and confinement size. In cases where the nanotubes are strongly attracted to one copolymer block, the confinement effect weakens as geometric space increases. Findings explain the dependence of chain conformation on the degree of confinement and the strength of surface preferences. [ABSTRACT FROM AUTHOR]