Self-assembly of three-legged patchy particles into polyhedral cages

2010 ◽  
Vol 22 (10) ◽  
pp. 104103 ◽  
Author(s):  
Wouter K den Otter ◽  
Marten R Renes ◽  
W J Briels
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.


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.


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.


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.


Langmuir ◽  
2016 ◽  
Vol 32 (31) ◽  
pp. 7929-7942 ◽  
Author(s):  
C. Salvador-Morales ◽  
Binal Brahmbhatt ◽  
V. Márquez-Miranda ◽  
I. Araya-Duran ◽  
J. Canan ◽  
...  

Soft Matter ◽  
2019 ◽  
Vol 15 (11) ◽  
pp. 2430-2438 ◽  
Author(s):  
Fatemeh Naderi Mehr ◽  
Dmitry Grigoriev ◽  
Nikolay Puretskiy ◽  
Alexander Böker

Not only in theory but also experimentally, mono-patchy particles can be self-assembled via pH-controlled electrostatic attractions between their oppositely charged patchy and patch-free surfaces.


2014 ◽  
Vol 1622 ◽  
pp. 55-60 ◽  
Author(s):  
Jonathan Liu ◽  
C. Wyatt Shields ◽  
Oluwatosin Omofoye ◽  
Gabriel P. Lopez

AbstractColloids with anisotropic shape and properties can enable the assembly of advanced materials otherwise not attainable by microfabrication. In this study, we present a convenient method using common microfabrication tools to generate a diverse array of non-spherical microparticles with well-defined shapes, sizes, electromagnetic properties for self-assembly applications. Projection photolithography onto SU-8 photoresist enabled the production of large aspect ratio microparticles such as cubes, cuboids, cylinders, hexagonal prisms, and parallelepipeds. We characterized these particles to confirm their anisotropic shape and size monodispersity. Fluorescent stains (e.g., Nile red) were mixed into the photoresist prepolymer to enhance the visualization of particle orientation. Particles designed for passive self-assembly were prepared by conventional photolithographic techniques. Particles designed for active assembly were then decorated with metallic patches in precise locations along the surface (e.g., top, side or multiple sides) using electron beam metal evaporation. This metal deposition process can enable orientational control of particles during their assembly in directed fields. After fabrication, large particles (e.g., 1,000 µm3) were released from the substrate via gentle sheer forces, whereas small particles (e.g., 10 µm3) were released by the dissolution of a sacrificial layer underneath the SU-8. Suspending the particles in water with surfactant (or other suitable solvents) provided amenable conditions for their assembly in static or dynamic systems. These conventional methods have the potential to catalyze new research in the fabrication and assembly of anisotropic patchy particles with controllable properties for the hierarchical development of self-assembled micromirrors, biosensors, and photonic crystals as examples.


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