Display options
Share it on

Nanoscale. 2014 Jan 07;6(1):565-71. doi: 10.1039/c3nr05256g. Epub 2013 Nov 18.

Chemical force microscopy of stimuli-responsive adhesive copolymers.

Nanoscale

Audrey Beaussart, T Chinh Ngo, Sylvie Derclaye, Radostina Kalinova, Rosica Mincheva, Philippe Dubois, Philippe Leclère, Yves F Dufrêne

Affiliations

  1. Université catholique de Louvain, Institute of Life Sciences, Croix du Sud 1, bte L7.04.01., B-1348 Louvain-la-Neuve, Belgium. [email protected].

PMID: 24240173 DOI: 10.1039/c3nr05256g

Abstract

Atomic force microscopy with chemically sensitive tips was used to investigate the hydrophobic and electrostatic interaction forces of a stimuli-responsive adhesive polymer, and their dynamic changes in response to water immersion and salt concentration. Block copolymer-filled coatings were obtained by incorporating an amphiphilic block copolymer containing a polydimethylsiloxane (PDMS) block and a poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) block in a PDMS matrix. Topographic images of fresh samples revealed the presence of nanoscale domains associated with the presence of copolymers, covered by a thin layer of PDMS. Prolonged (30 days) immersion in aqueous solution led to the exposure of the hydrophilic PDMAEMA chains on the surface. Using adhesion force mapping with hydrophobic tips, we showed that fresh samples were uniformly hydrophobic, while aged samples exhibited lower surface hydrophobicity and featured nanoscale hydrophilic copolymer domains. Force mapping with negatively charged tips revealed remarkable salt-dependent force plateau signatures reflecting desorption of polyelectrolyte copolymer chains. These nanoscale experiments show how solvent-induced conformational changes of stimuli-responsive copolymers can be used to modulate surface adhesion.

Publication Types