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Nanoscale Contact Mechanics between Two Grafted Polyelectrolyte Surfaces
Author(s) -
Maryam Raftari,
Zhenyu J. Zhang,
Steven R. Carter,
Graham J. Leggett,
Mark Geoghegan
Publication year - 2015
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.5b01540
Subject(s) - adhesion , solvation , contact area , polyelectrolyte , electrostatics , methacrylate , chemistry , surface forces apparatus , chemical physics , materials science , chemical engineering , composite material , copolymer , solvent , polymer , organic chemistry , engineering
The adhesive and frictional behavior of end-grafted poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) films (brushes) in contact with atomic force microscope tips from which PDMAEMA or poly(methacrylic acid) (PMAA) were grafted has been shown to be a strong function of pH in aqueous solution. The interaction between the brush-coated surfaces is determined by a combination of electrostatic and noncovalent interactions, modulated by the effect of the solvation state on the brush and the resulting area of contact between the probe and the surface. For cationic PDMAEMA–PDMAEMA contacts at low pH, the brushes are highly solvated; a combination of electrostatic repulsion and a high degree of solvation (leading to a significant osmotic pressure) leads to a small area of contact, weak adhesion, and energy dissipation through plowing. As the pH increases, the electrostatic repulsion and the osmotic pressure decrease, leading to an increase in the area of contact and a concomitant increase in the strength of adhe...

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