Self-assembly of cubic colloidal particles at fluid-fluid interfaces by hexapolar capillary interactions.

Colloidal particles adsorbed at fluid-fluid interfaces can self-assemble, thanks to capillary interactions, into 2D ordered structures. Recently, it has been predicted by theoretical and numerical calculations [G. Soligno et al., Phys. Rev. Lett., 2016, 116, 258001] that cubes with smooth edges adsorbed at a flat fluid-fluid interface generate hexapolar capillary deformations that cause the particles to self-assemble into honeycomb and hexagonal lattices, at equilibrium and for Young's contact angle π/2. Here we extend these results. Firstly, we show that capillary interactions induced by hexapolar deformations can drive the particles at the interface to form also thermodynamically-stable square lattices, in addition to honeycomb and hexagonal lattices. Then, we study the effects of tuning the particle shape on the particle self-assembly at the interface, considering, respectively, smooth-edge cubes, sharp-edge cubes, slightly truncated-edge cubes, and highly truncated-edge cubes. In our calculations, both capillary and hard-particle interactions are taken into account. We show that such variations in the particle shape significantly affect both qualitatively and quantitatively the self-assembly of the particles at the interface, and we sum up our results in the form of temperature-density phase diagrams. For example, using typical experimental parameters, our results show that only 4-to-5 nm sized sharp-edge and smooth-edge cubes can self-assemble into a honeycomb lattice, while slightly and highly truncated-edge cubes can form a honeycomb lattice only if they have a 8-to-12 and 10-to-16 nm size, respectively, for the same experimental parameters. Also, our results show that the capillarity-induced square lattice phase is stable only for the smooth-edge and truncated-edge cubes, but not for the sharp-edge cubes.