Metastable orientational order of colloidal discoids

Lilian C. Hsiao, Benjamin A. Schultz, Jens Glaser, Michael Engel, Megan E. Szakasits, Sharon C. Glotzer, Michael J. Solomon

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

The interplay between phase separation and kinetic arrest is important in supramolecular self-assembly, but their effects on emergent orientational order are not well understood when anisotropic building blocks are used. Contrary to the typical progression from disorder to order in isotropic systems, here we report that colloidal oblate discoids initially self-assemble into short, metastable strands with orientational order - regardless of the final structure. The model discoids are suspended in a refractive index and density-matched solvent. Then, we use confocal microscopy experiments and Monte Carlo simulations spanning a broad range of volume fractions and attraction strengths to show that disordered clusters form near coexistence boundaries, whereas oriented strands persist with strong attractions. We rationalize this unusual observation in light of the interaction anisotropy imparted by the discoids. These findings may guide self-assembly for anisotropic systems in which orientational order is desired, such as when tailored mechanical properties are sought.

Original languageEnglish
Article number8507
JournalNature Communications
Volume6
DOIs
StatePublished - Oct 7 2015
Externally publishedYes

Funding

We thank E. Viges and G. van Anders for fruitful advice and discussion. L.C.H., M.E.S. and M.J.S. are supported by the National Science Foundation (NSF CBET 1232937). B.A.S., J.G., M.E. and S.C.G. are supported in part by the US Army Research Office under grant award W911NF-10-1-0518, and in part by the DOD/ASD(R&E) under award number N00244-09-1-0062. The simulation studies are supported by W911NF-1001-0518. Any opinions, findings and conclusions or recommendations expressed in this publication are those of the authors and do not necessarily reflect the views of the DOD/ASD(R&E). Part of this work used the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by National Science Foundation grant number ACI-105357562.

FundersFunder number
DOD/ASDN00244-09-1-0062, ACI-105357562
US Army Research OfficeW911NF-10-1-0518
National Science Foundation1232937, NSF CBET 1232937, 1053575

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