Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters










Database
Language
Publication year range
1.
ACS Nano ; 9(2): 1305-14, 2015 Feb 24.
Article in English | MEDLINE | ID: mdl-25634665

ABSTRACT

Moth's eye inspired multiscale ommatidial arrays offer multifunctional properties of great significance in optoelectronic devices. However, a major challenge remains in fabricating these arrays on large-area substrates using a simple and scalable technique. Here we present the fabrication of these multiscale ommatidial arrays over large areas by a distinct approach called sacrificial layer mediated nanoimprinting, which involves nanoimprinting aided by a sacrificial layer. The fabricated arrays exhibited excellent pattern uniformity over the entire patterned area. Optimum dimensions of the multiscale ommatidial arrays determined by the finite-difference time domain simulations served as the design parameters for replicating the arrays on glass. A broadband suppression of reflectance to a minimum of ∼1.4% and omnidirectional antireflection for highly oblique angles of incidence up to 70° were achieved. In addition, superhydrophobicity and superior antifogging characteristics enabled the retention of optical properties even in wet and humid conditions, suggesting reliable optical performance in practical outdoor conditions. We anticipate that these properties could potentially enhance the performance of optoelectronic devices and minimize the influence of in-service conditions. Additionally, as our technique is solely nanoimprinting-based, it may enable scalable and high-throughput fabrication of multiscale ommatidial arrays.


Subject(s)
Biomimetics/methods , Nanotechnology/methods , Optical Phenomena , Animals , Eye , Humidity , Hydrophobic and Hydrophilic Interactions , Moths , Polycarboxylate Cement/chemistry
2.
Lab Chip ; 13(12): 2405-13, 2013 Jun 21.
Article in English | MEDLINE | ID: mdl-23645079

ABSTRACT

Fluorescence excitation enhancement by plasmonic nanostructures such as gold nanohole arrays has been a hot topic in biosensing and bioimaging in recent years. However, the high throughput and high yield fabrication of precisely designed metal nanostructures for optimized fluorescence excitation remains a challenge. Our work is the first report combining nanopattern nickel mould fabrication and UV imprinting for gold nanostructure mass fabrication in high yield. We report our successful gold nanohole array mass fabrication on a 4'' glass wafer, by first fabricating a high fidelity nickel mould, then using the mould for UV nanoimprinting on a polymer coated on the glass, evaporating the gold film on the glass wafer, and lifting off the polymer to obtain a gold nanohole array on the glass. Our optimized process for wafer fabrication can achieve almost 100% yield from nanoimprinting to gold lift-off, while the fabricated nickel mould has >70% defect-free area with the rest having a few scattered defects. In our work, the size and pitch of the gold nanohole array are designed to enhance the fluorescent dye Alexa 647. When the fabricated gold nanohole array is used for prostate specific antigen (PSA) detection by establishing a sandwiched fluorescence assay on the gold surface, a detection limit of 100 pg ml(-1) is achieved, while with a same thickness of gold film, only 1 ng ml(-1) is detected.


Subject(s)
Biomarkers/analysis , Gold/chemistry , Immunoassay , Nanostructures/chemistry , Fluorescent Dyes/chemistry , Humans , Male , Nickel/chemistry , Prostate-Specific Antigen/analysis
3.
Opt Express ; 20(25): 27697-707, 2012 Dec 03.
Article in English | MEDLINE | ID: mdl-23262717

ABSTRACT

A wide-range split-ladder photonic crystal cavity which is tuned by changing its intrinsic gap width is designed and experimentally verified. Different from the coupled cavities that feature resonance splitting into symmetric and anti-symmetric modes, the single split-ladder cavity has only the symmetric modes of fundamental resonance and second-order resonance in its band gap. Finite-difference time-domain simulations demonstrate that bipolar resonance tuning (red shift and blue shift respectively) can be achieved by shrinking and expanding the cavity's gap, and that there is a linear relationship between the resonance shifts and changes in gap width. Simulations also show that the split-ladder cavity can possess a high Q-factor when the total number of air holes in the cavity is increased. Experimentally, comb drive actuator is used to control the extent of the cavity's gap and the variation of its displacements with applied voltage is calibrated with a scanning electron microscope. The measured wavelength of the second-order resonance shifts linearly towards blue with increase in gap width. The maximum blue shift is 17 nm, corresponding to a cavity gap increase of 26 nm with no obvious degradation of Q-factor.


Subject(s)
Electronics/methods , Models, Theoretical , Nanostructures/chemistry , Nanotechnology/methods , Optics and Photonics/methods , Silicon/chemistry , Crystallization/methods , Equipment Design , Lasers, Dye , Microscopy, Electron, Scanning , Microtechnology/methods
4.
Phys Rev E Stat Nonlin Soft Matter Phys ; 85(1 Pt 2): 015303, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22400617

ABSTRACT

A method to create impacting jets at the micrometer length scale by means of a collapsing cavitation bubble is presented. A focused shock wave from a lithotripter leads to the nucleation of a cavitation bubble below a hole of 25 µm diameter etched in a silicon plate. The plate is placed at an air-water interface. The expansion and collapse of the bubble leads to two separate jets--an initial slow jet of velocity ∼10 m/s and a later faster jet of velocity ∼50 m/s. The jets subsequently impact coaxially, resulting in a circular sheet of liquid in the plane perpendicular to their axis. The sheet is characterized by a ring of droplets at its rim and breaks up into a spray as the shock pressure is increased. The results demonstrate an approach to create a high-speed jet and fine spray on demand at the micrometer scale.

5.
Opt Express ; 18(21): 22232-44, 2010 Oct 11.
Article in English | MEDLINE | ID: mdl-20941125

ABSTRACT

Control of photonic crystal resonances in conjunction with large spectral shifting is critical in achieving reconfigurable photonic crystal devices. We propose a simple approach to achieve nano-mechanical control of photonic crystal resonances within a compact integrated on-chip approach. Three different tip designs utilizing an in-plane nano-mechanical tuning approach are shown to achieve reversible and low-loss resonance control on a one-dimensional photonic crystal nanocavity. The proposed nano-mechanical approach driven by a sub-micron micro-electromechanical system integrated on low loss suspended feeding nanowire waveguide, achieved relatively large resonance spectral shifts of up to 18 nm at a driving voltage of 25 V. Such designs may potentially be used as tunable optical filters or switches.

6.
Opt Lett ; 35(15): 2517-9, 2010 Aug 01.
Article in English | MEDLINE | ID: mdl-20680043

ABSTRACT

We present dynamic tuning of optical resonance using microelectromechanical systems (MEMS)-driven coupled photonic crystal (PhC) nanocavities. The device consists of an air-suspended one-dimensional PhC nanocavity coupled to input and output waveguides and a perturbing nanocavity attached to a submicrometer MEMS comb drive. Resonance tuning is achieved through varying the gap between the two coupled cavities. We demonstrate experimentally that resonance can be tuned up to 8nm with no significant deterioration in the Q factor. The proposed mechanism potentially enables a new platform of on-chip photonic devices that can achieve a large tuning range with low power and small footprint and may find useful applications in tunable optical/photonic devices.

7.
Stat Med ; 25(1): 3-22, 2006 Jan 15.
Article in English | MEDLINE | ID: mdl-16013039

ABSTRACT

We propose a dose-finding weighted design for an early clinical trial which aims to determine the optimal dose, selected on the basis of both efficacy and toxicity, to be used in patients entering subsequent studies in a drug development process. The goal is to identify the optimal dose, while using a minimal number of subjects. For each dose under test, a decision table is defined with a utility value attached to each possible decision. The relationship between the utility and the target probability for each outcome is shown. A Dirichlet prior is used and we illustrate the process of maximizing the expected utility under the resulting posterior distribution to find the optimal decision at each stage of the trial. We show how this affects the eventual choice of optimal dose in various scenarios. Properties of our design are discussed and compared with a current standard design.


Subject(s)
Bayes Theorem , Clinical Trials, Phase I as Topic/methods , Maximum Tolerated Dose , Anti-HIV Agents/administration & dosage , Child , Computer Simulation , HIV Infections/drug therapy , Humans , Research Design , Viral Load
SELECTION OF CITATIONS
SEARCH DETAIL
...