Differences between Tethered Polyelectrolyte Chains on Bare Mica and Hydrophobically Modified Mica

Authors

Marc Balastre
Phillip Schorr
J.-F. Argillier
Jinchuan Yang
Jimmy W. Mays
Matthew Tirrell

Date of this Version

2006

Comments

Published in Langmuir 2006, 22, 4084-4091.

Abstract

This study investigates the structures of layers of amphiphilic diblock copolymers of poly(t-butyl styrene)-poly- (styrene sulfonate) (PtBS-PSS) adsorbed on both the bare mica surface (hydrophilic) and an octadecyltriethoxysilane (OTE)-modified mica surface (hydrophobic). When the surface is rendered hydrophobic, the nonsoluble block exhibits stronger interaction with the surface and higher adsorbed masses are achieved. Interaction forces between two such adsorbed layers on both substrates were measured using the surface forces apparatus. The effect of salt concentration (Cs) and molecular weight (N) on the height of the self-assembled layers (L₀) was examined in each case. The resulting scaling relationship is in good agreement with predictions of the brush model, L₀ ∞ N^1.0 in the low-salt limit and L₀N^-1 ∞ (C_s/σ)^-0.32 in the salted regime, when adsorption takes place onto the hydrophobized mica surface. For adsorption on the bare mica surface, L₀N^-0.7 ∞ C_s ^-0.17 agrees with the scaling prediction of the sparse tethering model. The results suggest that, on the hydrophilic bare mica surface, the adsorbed amount is not high enough to form a brush structure and only very little intermolecular stretching of the tethered chains occurs; in contrast, the presence of the hydrophobic OTE layer increases the tethering density such that the polyelectrolyte chains adopt a brush conformation.