Effect of nanoparticle polydispersity on the self-assembly of polymer tethered nanospheres

Abstract

Recent simulations predict that aggregating nanospheres functionalized with polymer "tethers" can self-assemble to form a cylinder, perforated lamellae, lamellae, and even the double gyroid phase, which are phases also seen in block copolymer and surfactant systems. Nanoparticle size polydispersity is likely to be a characteristic of these systems. If too high, polydispersity may destabilize a phase. Using multiple thermodynamic paths to explore the phase diagram as a function of temperature and polydispersity, we explore the effect of nanosphere size polydispersity on the phase diagram. We show that in the portions of the phase diagram characterized by an icosahedral local nanoparticle packing motif, a low amount of polydispersity lowers the energy and a large amount of polydispersity raises the energy of the system by disrupting the icosahedral packing. In general, regions of the phase diagram characterized by liquid-like icosahedral packing have high terminal polydispersities from 15% to more than 30%. In the regions of the phase diagram characterized by crystalline local packing, polydispersity raises the energy of the system and induces a phase transition from crystalline to liquid-like ordering within the nanosphere rich regions of the microphase. We find the bilayer crystalline lamellae phase has a terminal polydispersity of 6%, but may still be partially crystalline up to 12%.