Tuning higher order structure in colloidal fluids.

Abstract

Colloidal particles self assemble into a wide range of structures under external AC electric fields due to induced dipolar interactions [Yethiraj and Van Blaaderen, <i>Nature</i>, 2003, <b>421</b>, 513]. As a result of these dipolar interactions, at low volume fraction the system is modulated between a hard-sphere like state (in the case of zero applied field) and a "string fluid" upon application of the field. Using both particle-resolved experiments and computer simulations, we investigate the emergence of the string fluid with a variety of structural measures including two-body and higher-order correlations. We probe the higher-order structure using three-body spatial correlation functions and a many-body approach based on minimum energy clusters of a dipolar-Lennard-Jones system. The latter constitutes a series of geometrically distinct minimum energy clusters upon increasing the strength of the dipolar interaction, which are echoed in the higher-order structure of the colloidal fluids we study here. We find good agreement between experiment and simulation at the two-body level. Higher-order correlations exhibit reasonable agreement between experiment and simulation, again with more discrepancy at higher field strength for three-body correlation functions. At higher field strength, the cluster population in our experiments and simulations is dominated by the minimum energy clusters for all sizes 8 ≤ <i>m</i> ≤ 12.