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Trapping, sorting, transportation, and manipulation of synthetic microparticles and biological cells enable investigations in their behavior and properties. Microfluidic techniques like rapid electrokinetic patterning (REP) provide a non-invasive means to probe into the nature of these micro and nanoparticles. The opto-electrically induced nature of a REP micro vortex allows tuning of the trap characteristics in real-time. In this work, we studied the effects of transient optical heating on the induced electrothermal vortex using micro-particle image velocimetry (μ-PIV) and computational modeling. A near infra-red (980 nm) laser beam was focused on a colloidal suspension of 1 μm polystyrene beads sandwiched between two parallel-plate electrodes. The electrodes were subjected to an AC current. The laser spot was scanned back-and-forth in a line, at different frequencies, to create the transient vortex. This phenomenon was also studied with a computational model made using COMSOL Multiphysics. We visualize fluid flow in custom-shaped REP traps by superposing multiple axisymmetric (spot) vortices and discuss the limitations of using superposition in dynamically changing traps.

The dynamic manipulation and assembly of colloids enables the advancement of analytical techniques in biotechnology and the development of self-assembled materials. Rapid electrokinetic patterning (REP) is a hybrid optoelectrokinetic technique that simultaneously uses a laser illumination and a uniform AC electric field to yield programmable, dynamic, and non-invasive manipulation of colloidal particles. Since it was introduced, the technique has been applied to microengineering and biological research fields, showing its promising capabilities as a great tool for trapping, aggregating, translating, and sorting single and multiple micro- and nanoparticles, including bacteria. To effectively leverage and enhance these applications, this review paper will highlight its versatility and capability, including REP’s principles, governing physics, different experimental setups, fabrications, applications, and future prospects.

Isomotive dielectrophoresis (isoDEP) is a unique DEP geometrical configuration where the gradient of the field-squared ( ∇ E rms 2 ) is constant. IsoDEP analyzes polarizable particles based on their magnitude and direction of translation. Particle translation is a function of the polarizability of both the particles and suspending medium, the particles' size and shape, and the frequency of the electric field. However, other electrokinetics act on the particles simultaneously, including electrothermal hydrodynamics. Hence, to maximize the DEP force relative to over electrokinetic forces, design parameters such as microchannel geometry, fabrication materials, and applied electric field must be properly tuned. In this work, scaling law analyses were developed to derive design rules, relative to particle diameter, to reduce unwanted electrothermal hydrodynamics relative to DEP-induced particle translation. For a particle suspended in 10 mS/m media, if the channel width and height are below ten particle diameters, the electrothermal-driven flow is reduced by ∼500 times compared to a channel that is 250 particles diameters in width and height. Replacing glass with silicon as the device's underlying substrate for an insulative-based isoDEP reduces the electrothermal induced flow approximately 20 times less.

Non-contact manipulation methods capable of trapping and transporting swimming bacteria can significantly aid in chemotaxis studies. However, high swimming speed makes the trapping of these organisms an inherently challenging task. We demonstrate that an optoelectric technique, rapid electrokinetic patterning (REP), can effectively trap and manipulate Enterobacter aerogenes bacteria swimming at velocities greater than 20 μm s(-1). REP uses electro-orientation, laser-induced AC electrothermal flow, and particle-electrode interactions for capturing these cells. In contrast to trapping non-swimming bacteria and inert microspheres, we observe that electro-orientation is critical to the trapping of the swimming cells, since unaligned bacteria can swim faster than the radially inward electrothermal flow and escape the trap. By assessing the cell membrane integrity, we study the effect of REP trapping conditions, including optical radiation, laser-induced heating, and the electric field on cell viability. When applied individually, the optical radiation and laser-induced heating have negligible effect on cells. At the standard REP trapping conditions fewer than 2% of cells have a compromised membrane after four minutes. To our knowledge this is the first study detailing the effect of REP trapping on cell viability. The presented results provide a clear guideline on selecting suitable REP parameters for trapping living bacteria.

Rapid electrokinetic patterning (REP) is an emerging optoelectric technique that takes advantage of laser-induced AC electrothermal flow and particle-electrode interactions to trap and translate particles. The electrothermal flow in REP is driven by the temperature rise induced by the laser absorption in the thin electrode layer. In previous REP applications 350-700 nm indium tin oxide (ITO) layers have been used as electrodes. In this study, we show that ITO is an inefficient electrode choice as more than 92% of the irradiated laser on the ITO electrodes is transmitted without absorption. Using theoretical, computational, and experimental approaches, we demonstrate that for a given laser power the temperature rise is controlled by both the electrode material and its thickness. A 25-nm thick Ti electrode creates an electrothermal flow of the same speed as a 700-nm thick ITO electrode while requiring only 14% of the laser power used by ITO. These results represent an important step in the design of low-cost portable REP systems by lowering the material cost and power consumption of the system.

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.

Reliable and simple techniques for rapid assembly and patterning of colloid architectures advance the discovery and implementation of such nanomaterials. This work demonstrates rapid electrokinetic two-dimensional assembly of colloidal structures guided by the geometry of thin film heaters within a parallel-plate device. This system is designed to enable either independently addressable or massively parallel colloidal assembly. A combination of electrothermal hydrodynamics, particle-electrode, and particle-particle electrokinetic interactions governs their assembly. Concentration and patterning of structures are shown with 1.0 μm polystyrene particles and sorting between 1.0 μm and 2.0 μm particles is demonstrated.

In the path toward the realization of carbon nanotube (CNT)-driven electronics and sensors, the ability to precisely position CNTs at well-defined locations remains a significant roadblock. Highly complex CNT-based bottom–up structures can be synthesized if there is a method to accurately trap and place these nanotubes. In this study, we demonstrate that the rapid electrokinetic patterning (REP) technique can accomplish these tasks. By using laser-induced alternating current (AC) electrothermal flow and particle–electrode forces, REP can collect and maneuver a wide range of vertically aligned multiwalled CNTs (from a single nanotube to over 100 nanotubes) on an electrode surface. In addition, these trapped nanotubes can be electrophoretically deposited at any desired location onto the electrode surface. Apart from active control of the position of these deposited nanotubes, the number of CNTs in a REP trap can also be dynamically tuned by changing the AC frequency or by adjusting the concentration of the dispersed nanotubes. On the basis of a calculation of the stiffness of the REP trap, we found an upper limit of the manipulation speed, beyond which CNTs fall out of the REP trap. This peak manipulation speed is found to be dependent on the electrothermal flow velocity, which can be varied by changing the strength of the AC electric field. A technique for precisely positioning nanostructures could enable intricate electronic devices. Carbon nanotubes are hollow cylinders of carbon atoms with excellent electrical properties. However, they are difficult to manipulate due to their ultrasmall size. Steve Wereley from Purdue University in the United States and his colleagues used a laser beam and an electric field to align carbon nanotubes on the surface of an electrode. The team’s technique—known as rapid electrokinetic patterning—works by trapping and translating nanotubes that are suspended in water between two electrodes. Laser light is used to heat a small volume of the liquid, which changes its permittivity and electrical conductivity. When combined with an electric field between the electrodes, this generates vortices that can trap single or multiple nanotubes. The nanotubes can then be dynamically positioned by moving the laser beam.

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 study a recently demonstrated AC electrokinetic technique for manipulation and concentration of colloidal particles on an electrode surface. The technique uses indium tin oxide (ITO)-based parallel-plate electrodes on which highly localized infrared (1064 nm) laser illumination is shone. We show that the highly localized laser illumination leads to a highly nonuniform heating of the electrode substrate, which in turn drives an electrothermal microvortex resulting in a rapid transport of particles toward the illuminated site. Hundreds of polystyrene particles, with diameters ranging from 2.0 to 0.1 microm, suspended in a low conductivity solution (2.0 mS/m) could be aggregated at selected locations on the electrode by activating the laser illumination at suitable AC frequencies. Subsequent deactivation of the laser illumination causes the particles to scatter, and we explore this dynamical behavior for 1.0 microm particles using Delaunay tessellations and high-speed videography. We establish that drag from the electrothermal microvortex acts against a repulsive force, which decreases with increasing AC frequency, to create stable particle clusters. Moreover, experimentally we show that this particle capturing technique can be characterized by a critical frequency: a frequency at which the captured colloidal particle cluster becomes unstable and particles are carried away into the bulk by the electrothermal microvortex. This critical frequency increases with decreasing particle diameter for similar particles. For 0.1 microm particles, comparison of aggregation at different AC frequencies is achieved by the comparison of fluorescent intensity profiles of the aggregations.

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.

Interdigitated electrodes are used in electrokinetic lab-on-a-chip devices for dielectrophoretic trapping and characterization of suspended particles, as well as the production of field-induced fluid flow via AC electroosomosis and electrothermal mechanisms. However, the optimum design for dielectrophoresis, that if symmetrical electrodes, cannot induce bulk electrohydrodynamic pumping. In addition, the mechanism of intrinsic electrothermal pumping is affected by the properties of the fluid, with thermal fields being generated by Joule Heating. This work demonstrates the incorporation of an underlying thin film heater, electrically isolated from the interdigitated electrodes by an insulator layer, to enhance bulk electrothermal pumping. The use of integrated heaters allows the thermal field generation to be controlled independently of the electric field. Numerical simulations are performed to demonstrate the importance of geometrical arrangement of the heater with respect to the interdigitated electrodes, as well as electrode size, spacing, and arrangement. The optimization of such a system is a careful balance between electrokinetics, heat transfer, and fluid dynamics. The heater location and electrode spacing influence the rate of electrothermal pumping significantly more than electrode width and insulator layer thickness. This demonstration will aid in the development of microfluidic electrokinetic systems that want to utilize the advantages associated with electrothermal pumping while simultaneously applying other lab-on-a-chip electrokinetics like dielectrophoresis.

Technologies that can enable concentration of low-abundance biomarkers are essential for early diagnosis of diseases. In this study, an optoelectrokinetic technique, termed Rapid Electrokinetic Patterning (REP), was used to enable dynamic particle manipulation in bead-based bioassays. Various manipulation capabilities, such as micro/nanoparticle aggregation, translation, sorting and patterning, were developed. The technique allows for versatile multi-parameter (voltage, light intensity and frequency) based modulation and dynamically addressable manipulation with simple device fabrication. Signal enhancement of a bead-based bioassay was demonstrated using dilute biotin–fluorescein isothiocyanate (FITC) solutions mixed with streptavidin-conjugated particles and rapidly concentrated with the technique. As compared with a conventional ELISA reader, the REP-enabled detection achieved a minimal readout of 3.87 nM, which was a 100-fold improvement in sensitivity. The multi-functional platform provides an effective measure to enhance detection levels in more bead-based bioassays.

A high aspect ratio 3D electrokinetic nanoprobe is used to trap polystyrene particles (200 nm), gold nanoshells (120 nm), and gold nanoparticles (mean diameter 35 nm) at low voltages (

The ability to manipulate small amounts of fluid is important for a variety of lab-on-a-chip applications. Electrokinetic microfluidic actuation methods, such as electrothermal pumping, are popular due to their simple implementation and reliability from no moving parts. Electrothermal motion in aqueous solutions results from the electric field acting upon dielectric inhomogeneities in the liquid induced by temperature gradients. The most traditional method of inducing temperature gradients is through direct Joule heating of the fluid itself, which is a function of the electrical conductivity of the liquid. In this case, the microelectrode geometry controls both the location of the Joule heating and the nature of the electric field. Therefore, it is impossible to independently control temperature and electric field with a single set of electrodes. A novel electrothermal microfluidic pump is demonstrated herein. The distinguishing feature of this electrothermal pump is an independent heating source using resistive heating of microfabricated metal traces. A second set of electrodes for electrothermal pumping have been layered on top of the electrically isolated heating elements. An arrangement of coplanar electrode strips with an additional resistive heating electrode was used to demonstrate electrothermal pumping. Fluid motion results were compared to established theory.Copyright © 2011 by ASME

ac electrokinetic manipulations of particles and fluids are important techniques in the development of lab-on-a-chip technologies. Most of these systems involve planar micro-electrode geometries, generating high strength electric fields. When these fields are applied to a dielectric medium, Joule heating occurs. Understanding electrothermal heating and monitoring the temperature in these environments are critical for temperature-sensitive investigations including biological applications. Additionally, significant changes in fluid temperature when subjected to an electric field will induce electrohydrodynamic flows, potentially disrupting the intended microfluidic profile. This work investigates heat generated from the interaction of ac electric fields and water at various electrical conductivities (from 0.92 mS/m to 390 mS/m). The electrode geometry is an indium tin oxide (ITO) electrode strip 20 μm wide and a grounded, planar ITO substrate separated by a 50 μm spacer with microfluidic features. Laser-induced fluorescence is used to measure the experimental changes in temperature. A normalization procedure that requires a single temperature-sensitive dye, Rhodamine B (RhB), is used to reduce uncertainty. The experimental electrothermal results are compared with theory and computer simulations.

Recently, we have demonstrated electrothermal hydrodynamics with an external heating source of a highly focused 1,064 nm laser beam [1]. This phenomenon, when coupled with particle-electrode electrokinetic interactions, has led to the rapid and selective concentration of suspended colloids [2–6]. This technique, termed Rapid Electrokinetic Patterning (REP) was demonstrated without any additional surface modification or patterning of the electrodes. This dynamic, optically induced fluid and particle manipulation technique could be used for a variety of lab-on-a-chip applications. However, there are additional effects that have yet to be investigated that are important for a complete understanding of REP. This paper showcases experimental particle-particle behavior observations by varying particle diameter, electrode material, and preliminary results of varying fluid electrical conductivity.

We utilize a simple parallel electrode setup on which intense holographic optical landscapes are shone. Intense optical illumination creates high local gradients in the dielectric properties of the fluid, which in the presence of an electric field results in a fluid body force. This leads to the creation of toroidal microvortices, which aid the particle concentration process. Fluid drag aiding low frequency AC electrokinetic forces leads to an aggregation of particles on the illuminated regions of the electrode surface. With a fine balance of these forces, we show that such optically driven electrokinetic mechanisms can capture and aggregate nanoparticles (50nm and 100 nm). Particle aggregation is a function of the AC frequency and by using fluorescent particles we characterize the technique as a function of the applied AC frequency. Relatively low optical powers (~20 mW) are utilized in this technique.

Recently, we have demonstrated a novel optically induced AC electrokinetic technique that rapidly, continuously and selectively concentrates micro and nanoparticles on an electrode surface [1–3]. This is demonstrated with a highly focused near-infrared (1,064 nm) laser beam applied to parallel plate electrodes separated by 50 μm without the need for photosensitive materials. This dynamic optically-induced technique can be applied towards a variety of lab-on-a-chip applications. This paper will explain the fundamental physical mechanisms involved, necessary in order to replicate and implement this technique. This dynamic fluid and particle manipulation technique may prove valuable to a variety of applications in micro- and nanotechnology.Copyright © 2009 by ASME

We demonstrate an optically induced electrokinetic technique that continuously concentrates nanoparticles on the surface of a parallel plate electrode that is biased with an AC signal. A highly focused beam of near-infrared light (1064 nm) was applied, inducing an electrothermal microfluidic vortex that carried nanoparticles to its center where they were accumulated. This technique was demonstrated with 49 nm and 100 nm fluorescent polystyrene particles and characterized as a function of applied AC frequency and voltage. With this technique the location and shape of colloidal concentration was reconfigured by controlling the optical landscape, yielding dynamic control of the aggregation. Colloidal concentration was demonstrated with a plain parallel plate electrode configuration without the need of photoconductive materials or complex microfabrication procedures.

Recently, we have demonstrated an optically induced AC electrokinetic technique that rapidly, continuously and selectively concentrates colloids on an electrode surface [1–3]. This is demonstrated with a highly focused near-infrared (1,064 nm) laser beam applied to parallel plate electrodes separated by 50 μm without any additional surface modification or patterning of the electrodes. This dynamic optically-induced technique can be applied towards a variety of lab-on-a-chip applications. This paper will explain its physical mechanisms and showcase recent results regarding its particle sorting capabilities. This dynamic, optically induced fluid and particle manipulation technique could be used for a variety of lab-on-a-chip applications.Copyright © 2009 by ASME

We show an optically induced AC electrokinetic technique that rapidly and continuously accumulates colloids on an electrode surface resulting in a crystalline-like monolayer aggregation. We demonstrate colloidal aggregation for particles ranging from 100 nm to 3 µm. Electrothermal hydrodynamics produce a microfluidic vortex that carries particles in suspension towards its center where they are trapped by low-frequency AC electrokinetic forces. We characterize the rate of particle aggregation as a function of the applied AC voltage and hence characterize trapping kinetics of this technique. We show that inter-particle distance varies with frequency and we explain this in the light of available theory.

AC electrokinetic manipulation of particles and fluids are important techniques in the development of lab-on-a-chip technologies. Most of these systems involve planar microelectrode geometries, generating high strength electric fields. When these fields are applied to a dielectric medium Joule heating occurs. Understanding electrothermal heating and monitoring the temperature in these environments is critical for temperature-sensitive investigations including biological applications. Additionally, significant changes in fluid temperature when subjected to an electric field will induce electrohydrodynamic flows, potentially disrupting the intended microfluidic profile. This work investigates heat generated from the interaction of AC electric fields and water at various electrical conductivities (from 0.92–390 mS/m). The electrode geometry is an ITO electrode strip 20 μm wide and a grounded, planar ITO substrate separated by a 50 μm spacer with microfluidic features. Laser Induced Fluorescence (LIF) is used to measure the experimental changes in temperature. A normalization procedure that requires a single temperature-sensitive dye, Rhodamine B (RhB), is proposed to reduce uncertainty. The experimental electrothermal results are compared to theory and computer simulations.

We demonstrate an optically induced ac electrokinetic technique that rapidly and continuously accumulates colloids on a parallel-plate electrode surface resulting in a crystalline-like aggregation. Electrothermal hydrodynamics produce a microfluidic vortex that carries suspended particles toward its center where they are trapped by local ac electrokinetic hydrodynamic forces. We characterize the rate of particle aggregation as a function of the applied ac voltage, ac frequency and illumination intensity. Hundreds of polystyrene particles (1.0 mu m) suspended in a low conductivity solution (2.4 mS m(-1)) were captured at a range of voltages (5-20 V-pp) and frequencies (20-150 kHz) with an optical power of approximately 20 mW. This technique was not restricted to near infrared (1064 nm) illumination and was also demonstrated at 532 nm. The sorting capability of this technique was demonstrated with a solution containing 0.5 mu m, 1.0 mu m and 2.0 mu m polystyrene particles. This dynamic optically induced technique rapidly concentrates, sorts and translates colloidal aggregates with a simple parallel-plate electrode configuration and can be used for a variety of lab-on-a-chip applications.

This fluid dynamics video showcases how optically induced electrokinetic forces can be used to drive three-dimensional micro-vortices. The strong microfluidic vortices are used constructively in conjunction with other electrokinetic forces to dynamically and rapidly aggregate particle groups. Particle manipulation is achieved on the surface of a parallel-plate gold/indium tin oxide (ITO) electrode that is illuminated with near-infrared (1064 nm) optical patterns and biased with a low frequency ($, Comment: Updated the abstract and added paragraph 2 and 3

We demonstrate an opto-electrokinetic technique for noninvasive particle manipulation on the surface of a parallel-plate indium tin oxide (ITO) electrode that is biased with an alternating current (AC) signal and illuminated with near-infrared (1064 nm) optical landscapes. This technique can generate strong microfluidic vortices at higher AC frequencies (> 100 kHz) and dynamically and rapidly aggregate and pattern particle groups at low frequencies (< 100 kHz).