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Rapid electrokinetic patterning (REP) is a technique for creating self-assembled monolayers (SAMs) of spherical particles in a liquid medium, and dynamically controlling them though the simultaneous application of an electric field and optically induced temperature gradients. Previous work has investigated and characterized REP axisymmetric aggregations generated from a focus laser within a uniform electric field; work herein characterizes line-shaped particle assemblies derived from the application of a linearly scanned laser. The resulting aggregations of spherical polystyrene particles (1 μm) suspended in low-conductivity aqueous potassium chloride solution (KCl, 2.5 mS/m) resembled elliptical-shaped crystalline geometries. The mean particle-to-particle spacing within the aggregation remained greater than 1.5 diameters for experiments herein (6.5 Vrms , 30 kHz) due to dipole-dipole repulsive forces. Interparticle spacing demonstrated a linear relationship (1.6-2.1 μm) with increasing scanning lengths (up to 83 μm), decreased from 1.9 to 1.7 μm with increasing scanning frequency (0.38-16 Hz) for a 53 μm scan length, and decreased from 2.0 to 1.6 μm with increasing laser power (11.9-18.8 mW) for a 59 μm, 16 Hz laser scan.

Optically-based lab-on-a-chip systems have the distinct advantage of being dynamically controlled in real time, providing reconfigurable operations that can be tuned to perform a variety of tasks. This manuscript demonstrates the concentration of liquid-suspended microparticles using a focused near-infrared laser (980 nm) and a parallel-plate electrode system. The parallel-plate electrodes consisted of an indium tin oxide-coated coverslip and a gold-coated glass substrate. When the laser was applied at 36 mW, the indium tin oxide surface is locally heated creating sharp temperature gradients on the order of 0.07(o) C/μm. When an AC field was applied, electrothermal hydrodynamic forces generated microfluidic vortices. At an AC frequency of 40 kHz, the optically controlled electro-hydrodynamics aggregated colloids at the center of fluid motion on the surface of the indium tin oxide coverslip. The nature of colloid aggregation, translation, and patterning was explored when the translational velocity of the laser spot was varied. This manuscript describes the design of the laser scanning system using commercially available components and the fabrication of the parallel-plate chip. The effect that the laser scanning rate has on the heat transfer, fluid velocity, and colloid aggregation is discussed.

We report the results of a study characterizing the behavior of colloid aggregations under manipulation of a technique known as Rapid Electrokinetic Patterning (REP) – this technique is capable of dynamically manipulating the crystallinity of 2D colloid aggregations, potentially enabling dynamically tunable photonic crystals. Herein, aggregations of spherical polystyrene particles 1.0 μm in diameter suspended in a low conductivity aqueous solution were collected at the surface of an indium-tin oxide coated glass slide. The uniform AC field coupled with laser-induced heating produced electrothermal hydrodynamics which is responsible for the self-assembly characteristics of the planar colloidal aggregation. REP was characterized experimentally by analyzing the mutual particle spacing within the aggregation as a function of the AC signal and laser power. Numerical simulations justified the assumption that the primary forces responsible for colloidal patterning herein are Stokes drag forces and dipole–dipole repulsive forces.