Interaction forces and molecular adhesion between pre-adsorbed poly(ethylene imine) layers
Interaction forces between pre-adsorbed layers of branched poly(ethylene imine) (PEI) of different molecular mass were studied with the colloidal probe technique, which is based on atomic force microscopy (AFM). During approach, the long-ranged forces between the surfaces are repulsive due to overlap of diffuse layers down to distances of a few nanometers, whereby regulation of the surface charge is observed. The ionic strength dependence of the observed diffuse layer potentials can be rationalized with a surface charge of 2.3 mC/m(2). The forces remain repulsive down to contact, likely due to electro-steric interactions between the PEI layers. These electro-steric forces have a range of a few nanometers and appear to be superposed to the force originating from the overlap of diffuse layers. During retraction of the surfaces, erratic attractive forces are observed due to molecular adhesion events (i.e., bridging adhesion). The frequency of the molecular adhesion events increases with increasing the ionic strength. The force response of the PEI segments is dominated by rubber-like extension profiles. Strong adhesion forces are observed for low molecular mass PEI at short distances directly after separation, while for high molecular mass weaker adhesion forces at larger distances are more common. The work of adhesion was estimated by integrating the retraction force profiles, and it was found to increase with the ionic strength. (c) 2005 Elsevier Inc. All rights reserved.
Keywords: surface forces ; branched polyelectrolytes ; adhesion ; colloidal probe microscopy ; Polyelectrolyte Multilayer Films ; Self-Assembly Process ; Silica Surfaces ; Adsorbed Polymer ; Charged Surfaces ; Glass Surfaces ; Mica Surfaces ; atomic force microscopy ; charge regulation ; poly(ethylene imine)
Record created on 2010-05-12, modified on 2016-08-08