The deposition of positively charged latex particles with radii between 20 and 100 nm on a negatively
charged mica surface is investigated with atomic force microscopy at low ionic strengths. The polystyrene
latex spheres with amidine headgroups are characterized as to their size distribution, electrophoretic
mobility, and aggregation behavior. Surface coverage measurements take into account the polydispersity
of the particles on the surface. Deposition kinetics from a quiescent solution are, for low coverage, in good
agreement with diffusion-limited adsorption. At long times, the surface coverage tends toward a maximum
surface coverage θmax independent of the particle concentration but depending on ionic strength. This
work extends the available data for θmax for small particle size and very low ionic strengths. The values
for θmax decrease with decreasing ionic strength; this trend is described with a simple model based on
random sequential adsorption and the effect of overlapping double layers. Particle size polydispersity can
modify the results for θmax substantially; its influence is investigated in detail.
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