Microphase Segregation in Polyelectrolyte Brushes

TL;DR

This paper uses self-consistent field theory to explore how electrostatic and hydrophobic interactions cause microphase segregation in polyelectrolyte brushes, revealing layered structures and their experimental signatures.

Contribution

It introduces a theoretical framework for predicting microphase-segregated morphologies in polyelectrolyte brushes, linking structure to measurable reflectivity spectra.

Findings

High grafting density leads to layered morphologies.

Transitions between morphologies are discontinuous.

Reflectivity spectra are sensitive to layer number and interface sharpness.

Abstract

Polyelectrolyte (PE) brushes have ubiquitous applications as surface modifiers which regulate various structural and dynamic properties. Here, we apply a continuous-space self-consistent field theory to study the structural heterogeneity in PE brushes induced by competing electrostatic and hydrophobic interactions. For brushes with high grafting densities, we find a series of microphase-segregated morphologies with alternating polymer-rich and polymer-poor layers in the direction normal to the substrate. The transitions between multi-layer morphologies with consecutive numbers of condensed layers as well as the melting transition to the fully swollen brush are all discontinuous. We also elucidate that the segregated layers are formed by different subpopulations of all chains, significantly different from the scenario of the pearl-necklace structure formed by a single PE in poor solvents. Furthermore, we bridge the microstructure of multi-layer brushes to experimentally measurable reflectivity spectra, where the oscillation period and amplitude in the spectra are shown to be very sensitive to the number of layers and the sharpness of the polymer-solvent interface. The multi-layer morphology predicted by our theory is in good agreement with the lamellae structure experimentally observed at hydrated Nafion film interfaces.