Order-disorder transitions in colloidal systems are an attractive option for making switchable materials. Electric-field-driven order-disorder transitions are especially attractive for this purpose because the tuning parameter is easily and externally controllable. However, precise positional control of 3D structure is immensely challenging. Using patterned electrodes, we demonstrate that ac electric fields-dominantly dielectrophoresis (DEP) coupled with an electrohydrodynamic mechanism consisting of induced-charge electro-osmosis (ICEO)-can be used to template colloidal order dynamically in three dimensions. We find that the electric field geometry dictates the location, size, and shape of colloidal patterns and can produce patterns with surprising complexity.
© 2011 American Chemical Society