The Self-Assembly of Particles with Isotropic Interactions

This is an author-created, un-copyedited version of an article accepted for publication in Journal of Physics: Condensed Matter. The publisher is not responsible for any errors or omissions in this version of the manuscript or any version derived from it. The Version of Record is available online at http://dx.doi.org/10.1088/0953-8984/25/32/325101.A generic field-theoretic model for the self-assembly of particles with isotropic interactions, motivated by ideas in DNA-mediated colloidal assembly, is presented. A simplest possible system of colloids in explicit solvent is examined to determine the ability of non-connected particles to form complex nanometre or micron scale equilibrium structures in the absence of confounding kinetic effects. It is found that non-trivial morphologies are possible and that, for this effectively one component system, these parallel the phases of diblock copolymer melts for certain parameter choices, despite the absence of connectivity or packing frustration in the model. An explanation for the morphological similarity between these architecturally disparate systems is given. For other parameter choices, it is found that meta-stable and defected phases become more common, and that similarity with block copolymer morphologies decreases

The self-assembly of particles with isotropic interactions: Using DNA coated colloids to create designer nanomaterials

Copyright (2014) AIP Publishing. This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. The following article appeared in AIP Conference Proceedings 1590 and may be found at http://dx.doi.org/10.1063/1.4870223Self-consistent field theory equations are presented that are suitable for use as a coarse-grained model for DNA coated colloids, polymer-grafted nanoparticles and other systems with approximately isotropic interactions. The equations are generalized for arbitrary numbers of chemically distinct colloids. The advantages and limitations of such a coarsegrained approach for DNA coated colloids are discussed, as are similarities with block copolymer self-assembly. In particular, preliminary results for three species self-assembly are presented that parallel results from a two dimensional ABC triblock copolymer phase. The possibility of incorporating crystallization, dynamics, inverse statistical mechanics and multiscale modelling techniques are discussed

The Self-Assembly of Particles with Isotropic Interactions

This is an author-created, un-copyedited version of an article accepted for publication in Journal of Physics: Condensed Matter. The publisher is not responsible for any errors or omissions in this version of the manuscript or any version derived from it. The Version of Record is available online at http://dx.doi.org/10.1088/0953-8984/25/32/325101.A generic field-theoretic model for the self-assembly of particles with isotropic interactions, motivated by ideas in DNA-mediated colloidal assembly, is presented. A simplest possible system of colloids in explicit solvent is examined to determine the ability of non-connected particles to form complex nanometre or micron scale equilibrium structures in the absence of confounding kinetic effects. It is found that non-trivial morphologies are possible and that, for this effectively one component system, these parallel the phases of diblock copolymer melts for certain parameter choices, despite the absence of connectivity or packing frustration in the model. An explanation for the morphological similarity between these architecturally disparate systems is given. For other parameter choices, it is found that meta-stable and defected phases become more common, and that similarity with block copolymer morphologies decreases