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Updated: Nov 6, 2025

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
Published on: May 15, 2017
Low Interfacial Free Energy Describes the Bulk Ordering Transition in Colloidal Cubes
Abhishek K Sharma1, Fernando A Escobedo1
1R. F. Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.
Abstract:
Many hard faceted nanoparticles are known to undergo disorder-to-order phase transitions following a classical nucleation and growth mechanism. In a previous study [J. Phys. Chem. B 2018, 122, 9264-9273], it was shown that hard cubes undergo a nonclassical phase transition with a bulk character instead of originating from consolidated nuclei. Significantly, an unusually high fraction of ordered particles was observed in the metastable basin of the disordered phase, even for very low degrees of supersaturation. This work aims to substantiate the conjecture that these unique properties originate from a comparatively low interfacial free energy between the disordered and ordered phases for hard cubes relative to other hard particle systems. Using the cleaving wall method to directly measure the interfacial free energy for cubes, it is found that its values are indeed small; e.g., at phase coexistence conditions, it is only one-fifth that for hard spheres. A theoretical nucleation model is used to explore the broader implications of low interfacial tension values and how this could result in a bulk ordering mechanism.
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