Flexible automated system for laser modified layer by layer assembly.

An open-source automated system for laser modified layer by layer assembly is described. This flexible system, the first designed to be used with this process, can be used to fabricate a range of laser patterned, layer by layer thin films. The Arduino microcontroller-based system features a stepper motor-controlled turntable that holds solutions and water rinses for dipping. The substrate can be moved vertically to be dipped into each of the solutions throughout the process. A semiconductor laser is used to modify the thickness of the thin film during the chosen dipping cycles. Several aspects of the robotic system are easily controlled via software, including the average laser power, irradiation time, horizontal laser position, and vertical substrate position. The system is fully automated and, once started, does not require any user interaction. To demonstrate the capability of the automated system for patterning, electrochromic thin film devices using 50-bilayer laser patterned films using the polymers poly(allylamine hydrochloride) and sodium poly[2-(3-thienyl)-ethoxy-4-butylsulfonate] are presented. One device is patterned with the shape of a large "C," created by irradiating the sample (55 mW average power, 405 nm) while the substrate was moved vertically up and down or the laser was moved horizontally. The laser irradiates the sample during only the dipping in the polycation polymer solution. A second electrochromic thin film device is based on a sample with five parallel laser patterned lines, where each line is fabricated with different average laser powers and, hence, different thicknesses. The thicknesses of the lines vary by about 30 nm.

Three-dimensional control of layer by layer thin films via laser modification.

A novel modification to the traditional layer by layer process that adds three-dimensional control to the technique is introduced. In this modification to the process, the substrate is irradiated with laser light during the polycation and/or polyanion dipping cycles. An array of PAH/PCBS polymer thin films were fabricated using the laser modified approach with varied bilayer numbers, laser powers, and laser irradiation times. The modification was conducted with a semiconductor laser with powers from 1.1 to 5.5 W at 450 nm. Surface profilometry results show a change in height of more than 500 nm for a 55 bilayer PAH/PCBS thin film. For 25 bilayer films, the addition of laser modification during the PAH cycle leads to a reduction in absorbance of up to 54% compared to the areas not being irradiated. The absorbance at 365 nm associated with PCBS shows a nonlinear relationship with bilayer number, in contrast to the usual linear relationship between absorbance and bilayer without laser irradiation. By adjusting irradiation time, irradiation power, number of bilayers, and the location of irradiation, a variety of structures with controlled thicknesses can be fabricated.

Optofluidic bioanalysis: fundamentals and applications.

Over the past decade, optofluidics has established itself as a new and dynamic research field for exciting developments at the interface of photonics, microfluidics, and the life sciences. The strong desire for developing miniaturized bioanalytic devices and instruments, in particular, has led to novel and powerful approaches to integrating optical elements and biological fluids on the same chip-scale system. Here, we review the state-of-the-art in optofluidic research with emphasis on applications in bioanalysis and a focus on waveguide-based approaches that represent the most advanced level of integration between optics and fluidics. We discuss recent work in photonically reconfigurable devices and various application areas. We show how optofluidic approaches have been pushing the performance limits in bioanalysis, e.g. in terms of sensitivity and portability, satisfying many of the key requirements for point-of-care devices. This illustrates how the requirements for bianalysis instruments are increasingly being met by the symbiotic integration of novel photonic capabilities in a miniaturized system.

Spectrally reconfigurable integrated multi-spot particle trap.

Optical manipulation of small particles in the form of trapping, pushing, or sorting has developed into a vast field with applications in the life sciences, biophysics, and atomic physics. Recently, there has been increasing effort toward integration of particle manipulation techniques with integrated photonic structures on self-contained optofluidic chips. Here, we use the wavelength dependence of multi-spot pattern formation in multimode interference (MMI) waveguides to create a new type of reconfigurable, integrated optical particle trap. Interfering lateral MMI modes create multiple trapping spots in an intersecting fluidic channel. The number of trapping spots can be dynamically controlled by altering the trapping wavelength. This novel, spectral reconfigurability is utilized to deterministically move single and multiple particles between different trapping locations along the channel. This fully integrated multi-particle trap can form the basis of high throughput biophotonic assays on a chip.

Hybrid optofluidic integration.

Complete integration of microfluidic and optical functions in a single lab-on-chip device is one goal of optofluidics. Here, we demonstrate the hybrid integration of a PDMS-based fluid handling layer with a silicon-based optical detection layer in a single optofluidic system. The optical layer consists of a liquid-core antiresonant reflecting optical waveguide (ARROW) chip that is capable of single particle detection and interfacing with optical fiber. Integrated devices are reconfigurable and able to sustain high pressures despite the small dimensions of the liquid-core waveguide channels. We show the combination of salient sample preparation capabilities-particle mixing, distribution, and filtering-with single particle fluorescence detection. Specifically, we demonstrate fluorescent labelling of λ-DNA, followed by flow-based single-molecule detection on a single device. This points the way towards amplification-free detection of nucleic acids with low-complexity biological sample preparation on a chip.

Optical particle sorting on an optofluidic chip.

We report size-based sorting of micro- and sub-micron particles using optical forces on a planar optofluidic chip. Two different combinations of fluid flow and optical beam directions in liquid-core waveguides are demonstrated. These methods allow for tunability of size selection and sorting with efficiencies as high as 100%. Very good agreement between experimental results and calculated particle trajectories in the presence of flow and optical forces is found.