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1.
Nanotechnology ; 28(6): 065301, 2017 Feb 10.
Article in English | MEDLINE | ID: mdl-28045006

ABSTRACT

This paper reports a liquid-free, mask-less electrochemical direct-write lithographic technique using an atomic force microscopy (AFM) probe for writing silver nanostructures in minutes on an optically transparent substrate. Under ambient conditions, silver is locally and controllably extracted to the surface of superionic (AgI)0.25 (AgPO3)0.75 glass by bringing a conductive AFM probe tip in contact with it, biasing the probe with a negative voltage, and regulating the resulting current. The growth mechanism of the resulting nanostructure is explored by extracting silver with a stationary AFM tip on the surface of the silver. A moving tip was then used to produce continuous lines, solid films and discrete dots of silver by implementing continuous and pulsed current writing approaches. The line dimensions depend on writing speed and current flowing in the electrochemical circuit, while the size and spacing of the dots depend on the parameters (magnitude, duration and frequency) of the current pulses and the writing speed of the AFM tip. Line-widths in the ∼100 nm range are demonstrated. Our investigation also shows that a threshold potential must be overcome to be able to draw and reduce silver ions on the glass surface. When polarity between the electrodes is reversed, the patterned silver ionizes back into the glass, thus offering the capability to erase and rewrite Ag patterns on the glass surface.

2.
Nano Lett ; 16(12): 7402-7407, 2016 12 14.
Article in English | MEDLINE | ID: mdl-27797522

ABSTRACT

The emergence and growth of transformation optics over the past decade has revitalized interest in how a gradient refractive index (GRIN) can be used to control light propagation. Two-dimensional demonstrations with lithographically defined silicon (Si) have displayed the power of GRIN optics and also represent a promising opportunity for integrating compact optical elements within Si photonic integrated circuits. Here, we demonstrate the fabrication of three-dimensional Si-based GRIN micro-optics through the shape-defined formation of porous Si (PSi). Conventional microfabrication creates Si square microcolumns (SMCs) that can be electrochemically etched into PSi elements with nanoscale porosity along the shape-defined etching pathway, which imparts the geometry with structural birefringence. Free-space characterization of the transmitted intensity distribution through a homogeneously etched PSi SMC exhibits polarization splitting behavior resembling that of dielectric metasurfaces that require considerably more laborious fabrication. Coupled birefringence/GRIN effects are studied by way of PSi SMCs etched with a linear (increasing from edge to center) GRIN profile. The transmitted intensity distribution shows polarization-selective focusing behavior with one polarization focused to a diffraction-limited spot and the orthogonal polarization focused into two laterally displaced foci. Optical thickness-based analysis readily predicts the experimentally observed phenomena, which strongly match finite-element electromagnetic simulations.

3.
Nanotechnology ; 23(17): 175303, 2012 May 04.
Article in English | MEDLINE | ID: mdl-22481526

ABSTRACT

We report fabrication and use of a flexible array of nano-apertures for photolithography on curved surfaces. The batch-fabricated apertures are formed of metal-coated silicone tips. The apertures are formed at the end of the silicone tips by either electrochemical etching of the metal or plasma etching of a protective mask followed by wet chemical etching. The apertures are as small as 250 nm on substrates larger than several millimeters. We demonstrate how the nano-aperture array can be used for nano-fabrication on flat and curved substrates, and show the subsequent fabrication steps to form large arrays of sub-micron aluminum dots or vertical silicon wires.

4.
Langmuir ; 23(5): 2906-14, 2007 Feb 27.
Article in English | MEDLINE | ID: mdl-17309225

ABSTRACT

We report here a technique to print small volumes of liquid on a hydrophobic substrate. This process is based on the control of the critical parameters that govern a quasi-equilibrium liquid transfer process from one surface to another. We present a qualitative model that describes the physics of a transfer printing process between hydrophobic surfaces, and we use the parameters outlined in this model to manipulate the amount of liquid transferred between surfaces. We demonstrate the printing of discrete, small volumes (approximately 70 fL) of different liquid inks on a polymer substrate starting with volumes that are 8 orders of magnitude larger (a droplet of approximately 10 microL) in a simple two-step procedure.

5.
Lab Chip ; 4(6): 576-80, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15570368

ABSTRACT

A microfluidic apparatus capable of creating continuous microscale cylindrical polymeric structures has been developed. This system is able to produce microstructures (e.g. fibers, tubes) by employing 3D multiple stream laminar flow and "on the fly"in-situ photopolymerization. The details of the fabrication process and the characterization of the produced microfibers are described. The apparatus is constructed by merging pulled glass pipettes with PDMS molding technology and used to manufacture the fibers and tubes. By controlling the sample and sheath volume flow rates, the dimensions of the microstructures produced can be altered without re-tooling. The fiber properties including elasticity, stimuli responsiveness, and biosensing are characterized. Responsive woven fabric and biosensing fibers are demonstrated. The fabrication process is simple, cost effective and flexible in materials, geometries, and scales.


Subject(s)
Acrylates/chemical synthesis , Biosensing Techniques/methods , Microchemistry/methods , Microfluidic Analytical Techniques/methods , Nanotubes/chemistry , Nanotubes/ultrastructure , Photochemistry/methods , Acrylates/chemistry , Acrylates/radiation effects , Biosensing Techniques/instrumentation , Elasticity , Equipment Design/methods , Equipment Failure Analysis , Light , Microchemistry/instrumentation , Microfluidic Analytical Techniques/instrumentation , Photochemistry/instrumentation , Shear Strength
6.
Philos Trans A Math Phys Eng Sci ; 362(1818): 1059-68, 2004 May 15.
Article in English | MEDLINE | ID: mdl-15306484

ABSTRACT

In this paper, an inexpensive, easy-to-fabricate active magnetic mixer is presented. This mixer functions on top of a common magnetic stir plate and is capable of mixing two streams, each at flow rates up to 5 ml min(-1). A liquid-phase photopolymerization technique is used to fabricate the device. An analysis of mixing efficiency is based on greyscale intensity measurements of two coloured streams passing through the mixer. A brief hypothesis of the mechanism of mixing is also presented.


Subject(s)
Complex Mixtures/chemistry , Magnetics/instrumentation , Microchemistry/instrumentation , Microfluidics/instrumentation , Nanotechnology/instrumentation , Equipment Design , Equipment Failure Analysis , Microchemistry/methods , Microfluidics/methods , Motion , Nanotechnology/methods , Rotation , Solutions
7.
Electrophoresis ; 25(10-11): 1705-13, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15188260

ABSTRACT

A fabrication platform for realizing integrated microfluidic devices is discussed. The platform allows for creating specific microsystems for multistep assays in an ad hoc manner as the components that perform the assay steps can be created at any location inside the device via in situ fabrication. The platform was utilized to create a prototype microsystem for detecting botulinum neurotoxin directly from whole blood. Process steps such as sample preparation by filtration, mixing and incubation with reagents was carried out on the device. Various microfluidic components such as channel network, valves and porous filter were fabricated from prepolymer mixture consisting of monomer, cross-linker and a photoinitiator. For detection of the toxoid, biotinylated antibodies were immobilized on streptavidin-functionalized agarose gel beads. The gel beads were introduced into the device and were used as readouts. Enzymatic reaction between alkaline phosphatase (on secondary antibody) and substrate produced an insoluble, colored precipitate that coated the beads thus making the readout visible to the naked eye. Clinically relevant amounts of the toxin can be detected from whole blood using the portable enzyme-linked immunosorbent assay (ELISA) system. Multiple layers can be realized for effective space utilization and creating a three-dimensional (3-D) chaotic mixer. In addition, external materials such as membranes can be incorporated into the device as components. Individual components that were necessary to perform these steps were characterized, and their mutual compatibility is also discussed.


Subject(s)
Botulinum Toxins/analysis , Enzyme-Linked Immunosorbent Assay/methods , Microfluidics/instrumentation , Software , Antibodies/immunology , Botulinum Toxins/blood , Sepharose/chemistry
8.
Annu Rev Biomed Eng ; 4: 261-86, 2002.
Article in English | MEDLINE | ID: mdl-12117759

ABSTRACT

Fluid flow at the microscale exhibits unique phenomena that can be leveraged to fabricate devices and components capable of performing functions useful for biological studies. The physics of importance to microfluidics are reviewed. Common methods of fabricating microfluidic devices and systems are described. Components, including valves, mixers, and pumps, capable of controlling fluid flow by utilizing the physics of the microscale are presented. Techniques for sensing flow characteristics are described and examples of devices and systems that perform bioanalysis are presented. The focus of this review is microscale phenomena and the use of the physics of the scale to create devices and systems that provide functionality useful to the life sciences.


Subject(s)
Microchemistry/methods , Miniaturization/instrumentation , Miniaturization/methods , Models, Theoretical , Rheology/methods , Biosensing Techniques/instrumentation , Biosensing Techniques/methods , Electrophoresis, Capillary/instrumentation , Electrophoresis, Capillary/methods , Equipment Design/methods , Immunoassay/instrumentation , Immunoassay/methods , Macromolecular Substances , Photography/instrumentation , Photography/methods , Rheology/instrumentation , Sequence Analysis, DNA/instrumentation , Sequence Analysis, DNA/methods
9.
Lab Chip ; 2(1): 50-5, 2002 Feb.
Article in English | MEDLINE | ID: mdl-15100862

ABSTRACT

We present a method for the ultra rapid prototyping of microfluidic systems using liquid phase photopolymerization, requiring less than 5 min from design to prototype. Microfluidic device fabrication is demonstrated in a universal plastic or glass cartridge. The method consists of the following steps: introduction of liquid prepolymer into the cartridge, UV exposure through a mask to define the channel geometry, removal of unpolymerized prepolymer, and a final rinse. Rapidly fabricated masters for polydimethylsiloxane micromolding are also demonstrated. The master making process is compared to SU-8 50 photoresist processes. Press-on connectors are developed and demonstrated. All materials used are commercially available and low cost. An extension of these methods (mix and match) is presented that allows for maximal design flexibility and integration with a variety of existing fluidic geometries, components, and processes.

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