Nanoparticles adsorbed at the water/oil interface: coverage and composition effects on structure and diffusion.

Dissipative particle dynamics simulations are performed to study the structural and dynamical properties of various systems of nanoparticles accumulated at the water/oil interface. Homogeneous and Janus nanoparticles with different surface compositions are studied. For all nanoparticles, as the surface density increases, a transition from a liquidlike to a solidlike state is observed, as expected. At a high density of nanoparticles, hexagonal structures emerge and the nanoparticles' self-diffusion coefficient decreases because of caging effects. Similar results are observed for nanoparticles with different surface chemistry. Because different nanoparticles have different contact angles at the water/oil interface, the results obtained for systems containing mixed nanoparticles are more interesting. For example, our results show that the self-diffusion coefficient is not a monotonic function of the system composition, caused by the complex relation between hydrodynamic interactions and effective nanoparticle-nanoparticle interactions.