Nanophotonic split-ring resonators as dichroics for molecular spectroscopy

The unique optical properties of metallic nanostructures have enabled the creation of a new generation of ultra sensitive biosensors based on vibrational spectroscopy. Through strict engineering of structural morphology, a nanometal’s free electrons can be tuned to resonate at a particular frequency, resulting in amplification and confinement of the electromagnetic field around certain areas of the structure. Molecules situated within these areas experience a greater degree of polarisation due to the oscillating plasmon field, a phenomena which, when combined with resonance Raman spectroscopy, has been shown to enable single molecule detection.1, 2 This thesis describes the fabrication and plasmonic characterisation of Au and Ag circular nano split-ring resonators using a combination of electron beam lithography, finite difference time domain simulation and transmission spectroscopy. Through alteration of ring radius, arc length, wall width, metal thickness and metallic composition it is shown that the asymmetric split-ring structures exhibit a multi-modal, polarisation dependent plasmonic response that can be tuned over several microns. Such a response enables these geometries to be employed as novel multi-wavelength biosensors via surface enhanced Raman spectroscopy and surface enhanced resonance Raman spectroscopy. This work goes on to demonstrate that by using electron beam lithography to manipulate the nano-scale geometry of Ag split-ring resonators, their optical properties can be tuned such that the structures exhibit two independently addressable, high frequency plasmon resonance modes for SERRS. In a series of sensing experiments it is shown that this tailored, multi-modal, polarisation dependent activity enables the split-rings to act as discriminating sensors, with each resonance tuned for a particular sensing purpose. Ultimately the structures are used as multi-wavelength, multi-analyte DNA SERRS sensors, with each resonance tuned both to the absorption wavelength of a differently coloured Raman reporter molecule and its corresponding laser excitation wavelength. In doing so, the ability of each resonance to independently sense clinically relevant concentrations of single DNA strand types from within a mixed population on the sensor surface is demonstrated

Dual color plasmonic pixels create a polarization controlled nano color palette

Color filters based upon nanostructured metals have garnered significant interest in recent years, having been positioned as alternatives to the organic dye-based filters which provide color selectivity in image sensors, as nonfading “printing” technologies for producing images with nanometer pixel resolution, and as ultra-high-resolution, small foot-print optical storage and encoding solutions. Here, we demonstrate a plasmonic filter set with polarization-switchable color properties, based upon arrays of asymmetric cross-shaped nanoapertures in an aluminum thin-film. Acting as individual color-emitting nanopixels, the plasmonic cavity-apertures have dual-color selectivity, transmitting one of two visible colors, controlled by the polarization of the white light incident on the rear of the pixel and tuned by varying the critical dimensions of the geometry and periodicity of the array. This structural approach to switchable optical filtering enables a single nanoaperture to encode two information states within the same physical nanoaperture, an attribute we use here to create micro image displays containing duality in their optical information states

Bridging the gap: rewritable electronics using real-time light-induced dielectrophoresis on lithium niobate

In the context of micro-electronics, the real-time manipulation and placement of components using optics alone promises a route towards increasingly dynamic systems, where the geometry and function of the device is not fixed at the point of fabrication. Here, we demonstrate physically reconfigurable circuitry through light-induced dielectrophoresis on lithium niobate. Using virtual electrodes, patterned by light, to trap, move, and chain individual micro-solder-beads in real-time via dielectrophoresis, we demonstrate rewritable electrical contacts which can make electrical connections between surface-bound components. The completed micro-solder-bead bridges were found to have relatively low resistances that were not solely dominated by the number of interfaces, or the number of discrete beads, in the connection. Significantly, these connections are formed without any melting/fusing of the beads, a key feature of this technique that enables reconfigurability. Requiring only a low-power (~3.5 mW) laser source to activate, and without the need for external power supply or signal generation, the all-optical simplicity of virtual-electrodes may prove significant for the future development of reconfigurable electronic systems

Polarization switchable two-color plasmonic nano-pixels for creating optical surfaces encoded with dual information states

We demonstrate tunable, polarization-dependent, dual-color plasmonic filters based upon arrays of asymmetric cross-shaped nano-apertures. Acting as individual color emitting nano-pixels, each aperture can selectively transmit one of 2 colors, switched by controlling the polarization of white-light incident on the rear of each pixel. By tuning the dimensions of the pixels we build a polarization sensitive color palette at resolutions far beyond the diffraction limit. Using this switchable color palette we are able to generate complex optical surfaces encoded with dual color and information states; allowing us to embed two color images within the same unit area, using the same set of nanoapertures. © (2016) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only

Multilayered nanoplasmonic arrays for self-referenced biosensing

Nanostructured sensors based on localized surface plasmon resonance (LSPR) offer a number of advantages over other optical sensing technologies, making them excellent candidates for miniaturized, label-free chemical and biological detection. Highly sensitive to local refractive index changes, the resonance peaks of the nanosensors shift by different amounts when subject to different biological and chemical environments. Modifications to the nanostructure surface allow for the detection of specific molecules and chemicals with shifts so sensitive that the presence of single molecules can be detected. However, this extreme sensitivity has its drawbacks. Resonance shifts also occur because of temperature shifts, light-intensity fluctuations, and other environmental factors. To distinguish detection from drift, a secondary sensor region is often required. This often doubles the size of the device, requires two light sources and detectors (or complex optics), doubles the sample volume required (which may be expensive, or may not be possible if the sample quantity is limited), and subjects the reference to potential biofouling. Here, we present a new proof-of-concept multilayered LSPR sensor design that incorporates both a sensing layer and an encapsulated reference layer within the same region. By doing so, we are able to monitor and correct for sensor drift without the need for a secondary reference channel. We demonstrate the suitability of this sensor for sucrose concentration measurements and for the detection of biotin–avidin interactions, while also showing that the sensor can self-correct for drift. We believe that this multilayer sensor design holds promise for point-of-care diagnostics

Nanoplasmonic Ecosystem Sensors

Rapid advances in design, materials, and fabrication technologies over the past decade have allowed scientists to construct novel sensors to map and investigate the marine environment in new ways. This paper investigates the potential of nanoplasmonic sensors to further improve our understanding of marine ecosystems by providing information on pressing physical, chemical, and biological ocean parameters

Engineering molecularly-active nanoplasmonic surfaces for DNA detection via colorimetry and Raman scattering

We report a novel nanophotonic biosensor surface capable of both colorimetric detection and Raman-scattered detection of DNA infection markers at extreme sensitivities. Combining direct-write lithography, dip-pen nanolithography based DNA patterning, and molecular self-assembly, we create molecularly-active plasmonic nanostructures onto which metallic nanoparticles are located via DNA-hybridization. Arraying these structures enables optical surfaces that change state when contacted by specific DNA sequences; shifting the surface color while simultaneously generating strong Raman-scattering signals. Patterning the DNA markers onto the plasmonic surface as micro-scale symbols results in easily identifiable color shifts, making this technique applicable to multiplexed lab-on-a-chip and point-of-care diagnostic applications

Reversible DNA micro-patterning using the fluorous effect

We describe a new method for the immobilisation of DNA into defined patterns with sub-micron resolution, using the fluorous effect. The method is fully reversible via a simple solvent wash, allowing the patterning, regeneration and re-patterning of surfaces with no degradation in binding efficiency following multiple removal/attachment cycles of different DNA sequences

Whisky tasting using a bimetallic nanoplasmonic tongue

Metallic nanostructures are ideal candidates for optical tongue devices thanks to their chemical stability, the sensitivity of their plasmonic resonance to environmental changes, and their ease of chemical-functionalization. Here, we describe a reusable optical tongue comprised of multiplexed gold and aluminum nano-arrays; a bimetallic device which produces two distinct resonance peaks for each sensing region. Through specific modification of these plasmonic arrays with orthogonal surface chemistries, we demonstrate that a dual-resonance device allows us to halve sensor sizes and data-acquisition times when compared to single-resonance, monometallic devices. We applied our bimetallic tongue to differentiate off-the-shelf whiskies with > 99.7% accuracy by means of linear discriminant analysis (LDA). This advance in device miniaturization, functionalization, and multiplexed readout indicates nanoplasmonic tongues will have future applications in chemical mixture identification in applications where portability, reusability, and measurement speed are key

Size-scaling effects for microparticles and cells manipulated by optoelectronic tweezers

In this work, we investigated the use of optoelectronic tweezers (OET) to manipulate objects that are larger than those commonly positioned with standard optical tweezers. We studied the forces that could be produced on differently sized polystyrene microbeads and MCF-7 breast cancer cells with light-induced dielectrophoresis (DEP). It was found that the DEP force imposed on the bead/cell did not increase linearly with the volume of the bead/cell, primarily because of the non-uniform distribution of the electric field above the OET bottom plate. Although this size-scaling work focuses on microparticles and cells, we propose that the physical mechanism elucidated in this research will be insightful for other micro-objects, biological samples, and micro-actuators undergoing OET manipulation