Abstract

We investigate the effective interactions between two nanoparticles (or colloids) immersed in a solvent exhibiting two-phase separation. Using a non-local density functional theory, we determine the dependence of the effective potential on the separation of the nanoparticles when the solvent is near bulk two-phase coexistence. If identical nanoparticles preferentially adsorbing phase αα are inserted into phase ββ, thick wetting layers of the preferable phase αα develop at their surfaces. At some particular separation hbh_b of the nanoparticles, the wetting layers connect to form a single bridge, and the induced effective potential becomes strongly attractive for all distances h<hbh<h_b. The bridging is a first order capillary condensation like transition for all radii of the nanoparticles greater than the critical radius RcR_c, the value of which was estimated to be approximately Rc≈20σR_c\approx20σ for a temperature T/Tc≈0.9T/T_c\approx0.9, where σσ is the size of the solvent (square-well) particles. For radii R<RcR<R_c the process of bridging is continuous. If the same particles are inserted into the preferable phase αα, the only effective interaction between them is induced by the short-ranged depletion potential. If the nanoparticles have opposite adsorption preferences, only a single wetting layer forms around one of the nanoparticles and the effective interaction is strongly repulsive in both phases. The repulsion, induced by a disruption of the wetting film by the presence of the second particle, is larger and slightly longer-ranged in a low density state.

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