学术文献库

In this work we investigated the question of how the molecular nature of the dielectric media and the polymer-solvent dielectric mismatch affect the collapse of a polyelectrolyte chain in solution by means of dissipative particle dynamics simulations. First, we studied whether the explicit treatment of dielectric media as polar beads instead of homogeneous dielectric background results in a different system behavior. We showed that the explicit treatment of polar beads facilitates the chain collapse, i.e. it occurs at smaller values of the electrostatic strength parameter values $λ^2 \sim Q^2/(εkT)$. We believe that the main reason for such behavior is that the dielectric response is in fact a collective effect, and the "effective" dielectric permittivity is different from the bulk value when the charges are close to each other and/or the density of the charges is high enough. This implies that the value of $λ$ does not have a universal meaning due to the small-scale effects related to the presence of polar species; therefore, changing the total unit charge $Q$ or the temperature $kT$ is not equivalent to changing $ε$. Next, we investigated how the difference of the dielectric permittivities of the polymer chain and solvent affects the collapse. We showed the polar chain adapts less swollen conformations in the polyelectrolyte regime and collapses easier compared to the case of non-polar chain; the possible reasons for such behavior are discussed.