Entropically driven self-assembly of pear-shaped nanoparticles

Philipp Wilhelm Albert Schönhöfer

This thesis addresses the entropically driven colloidal self-assembly of pear-shaped particle ensembles, including the formation of nanostructures based on triply periodic minimal surfaces, in particular of the Ia3d gyroid. One of the key results is that the formation of the Ia3d gyroid, re-ported earlier in the so-called pear hard Gaussian overlap (PHGO) approximation and confirmed here, is due to a slight non-additivity of that potential; this phase does not form in pears with true hard-core potential. First, we computationally study the PHGO system and present the phase diagram of pears with an aspect ratio of 3 in terms of global density and particle shape (degree of taper), containing gyroid, isotropic, nematic and smectic phases. We confirm that it is adequate to interpret the gyroid as a warped smectic bilayer phase. The collective behaviour to arrange into interdigitated sheets with negative Gauss curvature, from which the gyroid results, is investigated through correlations of (Set-)Voronoi cells and local curvature. This geometric arrangement within the bilayers suggests a fundamentally different stabilisation mechanism of the pear gyroid phase compared to those found in both lipid-water and di-block copolymer systems forming the Ia3d gyroid. The PHGO model is only an approximation for hard-core interactions, and we additionally investigate, by much slower simulations, pear-assemblies with true hard-core interactions (HPR). We find that HPR phase diagram only contains isotropic and nematic phases, but neither gyroid nor smectic phases. To understand this shape sensitivity more profoundly, the depletion interactions of both models are studied in two pear-shaped colloids dissolved in a hard sphere solvent. The HPR particles act as one would expect from a geometric analysis of the excluded-volume minimisation, whereas the PHGO particles show deviations from this expectation. These differences are attributed to the unusual angle dependency of the (non-additive) contact function and, more so, to small overlaps induced by the approximation. For the PHGO model, we further demonstrate that the addition of a small concentration of hard spheres ("solvent") drives the system towards a Pn3m diamond phase. This result is explained by the greater spatial heterogeneity of the diamond geometry compared to the gyroid where additional material is needed to relieve packing frustration. In contrast to copolymer systems, however, the solvent mostly aggregates near the diamond minimal surface, driven by the non-additivity of the PHGO pears. At high solvent concentrations, the mixture phase separates into “inverse” micelle-like structures with the blunt ends at the micellar centres and thin ends pointing out-wards. The micelles themselves spontaneously cluster, indicative of a hierarchical self-assembly process for bicontinuous structures. Finally, we develop a density functional for hard solids of revolution (including pears) within the framework of fundamental measure theory. It is applied to low-density ensembles of pear-shaped particles, where we analyse their response near a hard substrate. A complex orientational ordering close to the wall is predicted, which is directly linked to the particle shape and gives insight into adsorption processes of asymmetric particles. This predicted behaviour and the differences between the PHGO and HPR model are confirmed by MC simulations.

Entropically driven self-assembly of pear-shaped nanoparticles

Files and links (1)

Abstract

Details

Metrics