328535 Assembling Colloidal Clusters From Spherical Codes

Thursday, November 7, 2013: 4:20 PM
Union Square 14 (Hilton)
Carolyn L. Phillips, Argonne National Laboratory, Chicago, IL, Eric Jankowski, Chemical and Biological Engineering, University of Colorado at Boulder, Boulder, CO, Michelle Marval, Department of Material Science and Engineering, University of Michigan, Ann Arbor and Sharon C. Glotzer, Department of Chemical Engineering, University of Michigan, Ann Arbor, MI

Anisotropic building blocks assembled from colloidal particles are attractive building blocks for self-assembled materials because their complex interactions can be exploited to drive self-assembly. In this work we consider the thermodynamically driven self-assembly of terminal clusters of particles[1].  This assembly process forms self-limiting anisotropic clusters with well-defined structures.  We predict that clusters related to spherical codes, a mathematical sequence of points, can be synthesized via self assembly.   Using Brownian dynamics and free energy calculations we predict the expected cluster sizes and shapes as a function of temperature and ratio of particle diameter.  Structural and dynamical analysis of these tiny systems reveal rich and sometimes surprising properties.   For example, the equilibrium structure of a 5-cluster, a square pyramid arrangement is preferred over a more symmetric structure.  Our results suggest a promising way to assemble anisotropic building blocks from constituent colloidal spheres.

[1] C.L. Phillips, E. Jankowski, M. Marval and S.C. Glotzer, “Self-assembled clusters of spheres related to spherical codes,” Phys. Rev. E, 86 (4) 1124 (2012)


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See more of this Session: Colloidal Assembly and Device Fabrication
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