An optoelectronic tweezers (OETs) system employing a non-uniform background electric field is presented. In addition to optically induced electrodes, physical electrodes are incorporated into the design. The geometries of the physical electrodes are selected to create a background field with gradients along a specific axis. Due to the resulting background force, the proposed scheme traps particles along an axis around the rim of the optical spot. This is a resolution improvement over conventional OETs where particle trapping occurs uniformly around the spot. Numerical simulations of the device including conductivity, electric fields, and force profiles are presented. The trapping and manipulation of micro-particles using the device are experimentally demonstrated. The experiment verifies that trapping occurs along a specific axis of the optical beam.

We present a device that can achieve controlled transport of colloidal microparticles using an array of micro-electrodes. By exciting the micro-electrodes in regular sequence with an AC voltage, a time-varying moving dielectrophoretic force-field is created. This force propels colloidal microparticles along the electrode array. Using this method, we demonstrate bidirectional transport of polystyrene micro-spheres. Electromagnetic simulation of the device is performed, and the dielectrophoretic force profile around the electrode array is mapped. We develop a Brownian dynamics model of the trajectory of a particle under the influence of the time-varying force-field. Numerical and experimental results showing controlled particle transport are presented. The numerical model is found to be in good agreement with experimental data. The developed numerical framework can be useful in designing and modeling lab-on-a-chip devices that employ external non-contact forces for micro-/nanoparticle manipulation.

The non-conservative nature of the force field generated by a near-field optical trap is analyzed. A plasmonic C-shaped engraving on a gold film is considered as the trap. The force field is calculated using the Maxwell stress tensor method. The Helmholtz-Hodge decomposition is used to extract the conservative and the non-conservative component of the force. Due to the non-negligible non-conservative component, it is found that the conventional approach of extracting the potential by direct integration of the force is not accurate. Despite the non-conservative nature of the force field, it is found that the statistical properties of a trapped nanoparticle can be estimated from the conservative component of the force field alone. Experimental and numerical results are presented to support the claims.

Nanoparticles trapped on resonant near-field apertures/engravings carved in plasmonic films experience optical forces due to the steep intensity gradient field of the aperture/engraving as well as the image like interaction with the substrate. For non-resonant nanoparticles the contribution of the substrate interaction to the trapping force in the vicinity of the trap (aperture/engraving) mode is negligible. But, in the case of plasmonic nanoparticles, the contribution of the substrate interaction to the low frequency stable trapping mode of the coupled particle-trap system increases as their resonance is tuned to the trap resonance. The strength of the substrate interaction depends on the height of the nanoparticle above the substrate. As a result, a difference in back action mechanism arises for nanoparticle displacements perpendicular to the substrate and along it. For nanoparticle displacements perpendicular to the substrate, the self induced back action component of the trap force arises due to changing interaction with the substrate as well as the trap. On the other hand, for displacements along the substrate, it arises solely due to the changing interaction with the trap. This additional contribution of the substrate leads to more pronounced back action. Numerical simulation results are presented to illustrate these effects using a bowtie engraving as the near-field trap and a nanorod as the trapped plasmonic nanoparticle. The substrate’s role may be important in manipulation of plasmonic nanoparticles between successive traps of on-chip optical conveyor belts, because they have to traverse over regions of bare substrate while being handed off between these traps.

Lab-on-a-chip (LOC) devices capable of manipulating micro/nano-sized samples have spurred advances in biotechnology and chemistry. Designing and analyzing new and more advanced LOCs require accurate modeling and simulation of sample/particle dynamics inside such devices. In this work, we present a generalized computational physics model to simulate particle/sample trajectories under the influence of dielectrophoretic or optical forces inside LOC devices. The model takes into account time varying applied forces, Brownian motion, fluid flow, collision mechanics, and hindered diffusion caused by hydrodynamic interactions. We develop a numerical solver incorporating the aforementioned physics and use it to simulate two example cases: first, an optical trapping experiment, and second, a dielectrophoretic cell sorter device. In both cases, the numerical results are found to be consistent with experimental observations, thus proving the generality of the model. The numerical solver can simulate time evolution of the positions and velocities of an arbitrarily large number of particles simultaneously. This allows us to characterize and optimize a wide range of LOCs. The developed numerical solver is made freely available through a GitHub repository so that researchers can use it to develop and simulate new designs.

Solid-phase synthesis underpins many advances in synthetic and combinatorial chemistry, biology, and material science. The immobilization of a reacting species on the solid support makes interfacing of reagents an important challenge in this approach. In traditional synthesis columns, this leads to reaction errors that limit the product yield and necessitates excess consumption of the mobile reagent phase. Although droplet microfluidics can mitigate these problems, its adoption is fundamentally limited by the inability to controllably interface microbeads and reagent droplets. Here, we introduce Dielectrophoretic Bead-Droplet Reactor as a physical method to implement solid-phase synthesis on individual functionalized microbeads by encapsulating and ejecting them from microdroplets by tuning the supply voltage. Proof-of-concept demonstration of the enzymatic coupling of fluorescently labeled nucleotides onto the bead using this reactor yielded a 3.2-fold higher fidelity over columns through precise interfacing of individual microreactors and beads. Our work combines microparticle manipulation and droplet microfluidics to address a long-standing problem in solid-phase synthesis with potentially wide-ranging implications.