Using a two-dimensional self-consistent field calculation and scaling
theory, we investigate the interaction between two planar surfaces whe
re: (I) each surface is grafted with both solvophilic mid solvophobic
homopolymers and (2) both surfaces are coated with solvophobic polyele
ctrolytes. The chains are tethered by one end and grafted at relativel
y low densities. For both systems, we determine the morphology of the
layers and the energy of interaction as the layers are compressed. The
energy of interaction versus distance profiles show a wide region of
attraction as the surfaces are brought together. This attractive inter
action is due to the self-assembled structures that appear st low graf
ting densities in poor solvents. Furthermore, for polyelectrolytes at
high degrees of ionization (alpha), compressing the layers results in
a novel first-order phase transition: the uniformly stretched, charged
chains spontaneously associate into aggregates (pinned micelles) on t
he surfaces. At both low and high alpha, the free energy versus distan
ce profiles reveal distinct minima, which indicate an optimal separati
on between the surfaces. Our findings provide guidelines for controlli
ng the interactions between coated colloidal particles and yield desig
n criteria for driving colloids to self-assemble into ordered arrays.