Self-assembly of inverse patchy colloids with tunable patch coverage

2017 ◽  
Vol 19 (20) ◽  
pp. 13122-13132 ◽  
Author(s):  
Manigandan Sabapathy ◽  
Remya Ann Mathews K ◽  
Ethayaraja Mani

We report a simple and scalable technique for the preparation of patchy particles with tunable patch coverage.

2011 ◽  
Vol 45 (2) ◽  
pp. 1090-1106 ◽  
Author(s):  
Cristiano De Michele ◽  
Tommaso Bellini ◽  
Francesco Sciortino

Soft Matter ◽  
2014 ◽  
Vol 10 (45) ◽  
pp. 9167-9176 ◽  
Author(s):  
Gustavo A. Chapela ◽  
Orlando Guzmán ◽  
José Adrián Martínez-González ◽  
Pedro Díaz-Leyva ◽  
Jacqueline Quintana-H

A vibrating version of patchy particles in two dimensions is introduced to study self-assembly of kagome lattices, disordered networks of looping structures, and linear arrays.


2015 ◽  
Vol 112 (50) ◽  
pp. 15308-15313 ◽  
Author(s):  
Arthur C. Newton ◽  
Jan Groenewold ◽  
Willem K. Kegel ◽  
Peter G. Bolhuis

Predicting the self-assembly kinetics of particles with anisotropic interactions, such as colloidal patchy particles or proteins with multiple binding sites, is important for the design of novel high-tech materials, as well as for understanding biological systems, e.g., viruses or regulatory networks. Often stochastic in nature, such self-assembly processes are fundamentally governed by rotational and translational diffusion. Whereas the rotational diffusion constant of particles is usually considered to be coupled to the translational diffusion via the Stokes–Einstein relation, in the past decade it has become clear that they can be independently altered by molecular crowding agents or via external fields. Because virus capsids naturally assemble in crowded environments such as the cell cytoplasm but also in aqueous solution in vitro, it is important to investigate how varying the rotational diffusion with respect to transitional diffusion alters the kinetic pathways of self-assembly. Kinetic trapping in malformed or intermediate structures often impedes a direct simulation approach of a kinetic network by dramatically slowing down the relaxation to the designed ground state. However, using recently developed path-sampling techniques, we can sample and analyze the entire self-assembly kinetic network of simple patchy particle systems. For assembly of a designed cluster of patchy particles we find that changing the rotational diffusion does not change the equilibrium constants, but significantly affects the dynamical pathways, and enhances (suppresses) the overall relaxation process and the yield of the target structure, by avoiding (encountering) frustrated states. Besides insight, this finding provides a design principle for improved control of nanoparticle self-assembly.


Soft Matter ◽  
2018 ◽  
Vol 14 (7) ◽  
pp. 1162-1170
Author(s):  
V. Meester ◽  
D. J. Kraft

We investigate the mechanisms underlying the reconfiguration of random aggregates of spheres through capillary interactions, the so-called “colloidal recycling” method, for fabricating a wide variety of patchy particles. We explore the influence of capillary forces on clusters of deformable seed particles by systematically varying the crosslink density of the spherical seeds.


2019 ◽  
Vol 21 (42) ◽  
pp. 23447-23458 ◽  
Author(s):  
Manuella Cerbelaud ◽  
Khaoula Lebdioua ◽  
Công Tâm Tran ◽  
Benoît Crespin ◽  
Anne Aimable ◽  
...  

92 bead colloids are used to study the self-assembly of large surface anistropic particles.


Langmuir ◽  
2020 ◽  
Vol 36 (9) ◽  
pp. 2403-2418 ◽  
Author(s):  
Marlous Kamp ◽  
Bart de Nijs ◽  
Marjolein N. van der Linden ◽  
Isja de Feijter ◽  
Merel J. Lefferts ◽  
...  

Soft Matter ◽  
2020 ◽  
Vol 16 (15) ◽  
pp. 3806-3820 ◽  
Author(s):  
Yiwei Zhu ◽  
Artee Bansal ◽  
Shun Xi ◽  
Jinxin Lu ◽  
Walter G. Chapman

Novel theory incorporating multibody correlations accurately predicts aggregation and phase behavior in mixed Janus, Saturn ring, and Ternary patchy colloids.


Soft Matter ◽  
2019 ◽  
Vol 15 (46) ◽  
pp. 9394-9404
Author(s):  
Tobias M. Hain ◽  
Gerd E. Schröder-Turk ◽  
Jacob J. K. Kirkensgaard

Star copolymers on a sphere self-assemble into patchy particles with structure and coordination corresponding to those found in the famous Thomson problem.


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