Self-consistent field theory of polyelectrolyte brushes with finite chain extensibility

Abstract

Polyelectrolyte brushes are formed by charged macromolecules tethered by the end segment to a solid-liquid interface. At low ionic strength of the solution, the intermolecular electrostatic interactions lead to strong stretching of the macromolecules that may, as a result, approach the limit of their extensibility (the contour length). Here, we present an analytical theory of polyelectrolyte brushes developed within the Poisson-Boltzmann approximation which explicitly accounts for finite extensibility of the brush-forming chains. In contrast to earlier theories based on the approximation of Gaussian elasticity of the brush-forming chains, the current approach enables avoiding artificial result of stretching of the chains beyond the contour length at high degrees of ionization or/and large grafting densities.