Massive Enhancement of Optical Transmission across a Thin Metal Film via Wave Vector Matching in Grating-Coupled Surface Plasmon Resonance.

We demonstrate how distinct surface plasmon resonance modes on opposite sides of a metal-coated grating can be coupled across the metal film. This coupling occurs by matching the resonance conditions on each side of the grating by tuning the refractive index directly adjacent to the metal film. In the first example, we deposited a high refractive index layer of tin oxide on top of the grating to red-shift the front side surface plasmon until it coupled with the backside surface plasmon across a semitransparent ∼45 nm thin silver grating. By shifting the resonance condition of the nearby surface plasmon, this high refractive index coating creates an effective matching of wave vectors across the metal film, allowing them to couple and enhance the optical response. A massive increase in the magnitude of enhanced transmission is observed, increasing from a 6-fold transmission enhancement through a bare silver grating to a near 100-fold enhancement after deposition of a tin oxide layer of appropriate thickness (∼310 nm). This optical transmission enhancement is then probed through computational modeling and by experiments with liquids of various refractive index values. The matched system shows an increased amplitude sensitivity with respect to refractive index changes and a waveguide like behavior within the tin oxide film. As an alternative configuration, we also demonstrate coupling the front and back-side plasmon modes by using a lower refractive index substrate in order to blue-shift the back-side surface plasmon. Coupling between the two plasmon modes is then demonstrated by introducing aqueous solutions of various refractive index values. Under the proper conditions, this matched system also shows a substantial enhancement in transmission. This technique of wave vector matching provides a route to substantially increasing the plasmon enhanced optical transmission through metal gratings, which has potential application in improved plasmonic sensing, spectroscopy, and plasmon-based optical devices.

Experimental analysis of waveguide-coupled surface-plasmon-polariton cone properties.

Experimental data for waveguide-coupled surface-plasmon-polariton (SPP) cones generated from dielectric waveguides is presented. The results demonstrate a simpler route to collect plasmon waveguide resonance (i.e., PWR) data. In the reverse-Kretschmann configuration (illumination from the sample side) and Kretschmann configuration (illumination from the prism side), all the waveguide modes are excited simultaneously with p- or s-polarized incident light, which permits rapid acquisition of PWR data without the need to scan the incident angle or wavelength, in the former configuration. The concentric SPP cone properties depend on the thickness and index of refraction of the waveguide. The angular intensity pattern of the cone is well-matched to simulation results in the reverse-Kretschmann configuration, and is found to be dependent on the polarization of the incident light and the polarization of the waveguide mode. In the Kretschmann geometry, all waveguide-coupled SPP cones are measured at incident angles that produce attenuated light reflectivity. In addition, the enhanced electric field produced under total internal reflection allows high signal-to-noise ratio multimodal spectroscopies (e.g., Raman scattering, luminescence) to measure the chemical content of the waveguide film, which traditionally is not measured with PWR.

A phase-change thin film-tuned photonic crystal device.

This paper reports a tunable photonic device that incorporates a thin layer of phase-change material, Ge2Sb2Te5 (GST), in a photonic crystal (PC) structure. The PC structure is based on a one-dimensional grating waveguide with a metal cladding. The metal-cladded PC structure supports a guided-mode resonance (GMR) that selectively absorbs light at a particular wavelength. Inserting the GST material into the gating waveguide makes it possible to control the GMR mode. Here, the GST-PC device was numerically designed and optimized to obtain significant tuning of the GMR mode around 1550 nm. The tuning phenomena were experimentally demonstrated by the heat-induced phase change between crystalline and amorphous phases of the GST thin film. A spectral shift of the resonant wavelength from 1440 to 1610 nm was achieved via the crystallization process. The phase tuning of GST exhibits good repeatability as demonstrated by switching between amorphous and crystalline phases of GST for multiple cycles. The GST-PC device represents a new approach for tuning optical resonances with potential applications including but not limited to integrated photonic circuits, optical communications, and high-performance optical filters.

Templating Colloidal Crystal Growth Using Chirped Surface Relief Gratings.

We report a method for controlling the lattice geometry of monodisperse colloidal crystals formed by confined convective self-assembly on a substrate patterned with a chirped surface relief grating. Chirped gratings were fabricated using laser interference lithography and a curved mirror reflector to create photoresist patterns with pitch values ranging from ∼500 to >10 000 nm spread over a planar surface. These surface nanostructures are shown to guide the formation of various lattice geometries not normally found via colloidal assembly on planar surfaces. It is shown that when the pitch of the grating is much larger than the diameter of the colloidal particles, the grating trenches serve as compartments for deposition and the particles form close-packed, linear chains. Various ordered structures are observed as the dimensions of the grating pitch decrease and approach the diameter of the particles. The grating nanostructures guide the formation of various lattice geometries due to specific particle-surface and particle-particle interactions. Observed crystal lattices include square, hexagonal, and rhombic structures. The formation of these structures is explained in terms of the geometrical constraints imposed by the surface pattern and the particle diameter. These crystal lattices can be translated into large area samples when using corresponding single-pitch grating substrates. The initial monolayer lattice can also serve as a template for the growth of unique, bilayer structures that include rectangular lattices, chains of particle pairs or triplets, and graphitelike structured lattices. In addition, when coated with a thin silver layer, these various lattice configurations are shown to produce optical reflection features that are precisely controlled by the underlying structure as it varies from widely spaced particle chains to close-packed lattice geometries.

Food waste-to-energy conversion technologies: current status and future directions.

Food waste represents a significantly fraction of municipal solid waste. Proper management and recycling of huge volumes of food waste are required to reduce its environmental burdens and to minimize risks to human health. Food waste is indeed an untapped resource with great potential for energy production. Utilization of food waste for energy conversion currently represents a challenge due to various reasons. These include its inherent heterogeneously variable compositions, high moisture contents and low calorific value, which constitute an impediment for the development of robust, large scale, and efficient industrial processes. Although a considerable amount of research has been carried out on the conversion of food waste to renewable energy, there is a lack of comprehensive and systematic reviews of the published literature. The present review synthesizes the current knowledge available in the use of technologies for food-waste-to-energy conversion involving biological (e.g. anaerobic digestion and fermentation), thermal and thermochemical technologies (e.g. incineration, pyrolysis, gasification and hydrothermal oxidation). The competitive advantages of these technologies as well as the challenges associated with them are discussed. In addition, the future directions for more effective utilization of food waste for renewable energy generation are suggested from an interdisciplinary perspective.

Heterogeneous catalyst-assisted thermochemical conversion of food waste biomass into 5-hydroxymethylfurfural.

A novel thermochemical conversion route has been developed that yields 5-hydroxymethylfurfural (HMF) from food waste biomass (FWB) in the presence of a heterogeneous catalysts (zirconium phosphate (ZrP)). The ZrP catalyst was prepared by precipitation followed by calcination at 400 (ZrP-400) and 600 °C (ZrP-600) and was characterized by SEM, XRD, XPS, N2 sorption and NH3-TPD. The optimized reaction conditions were identified to maximize HMF yield by varying the type of catalyst, the catalyst loading and the reaction time. The highest HMF yield achieved was 4.3%. On average 33% higher yield for ZrP-600 was obtained compared to that for ZrP-400, which might be due to higher number of acid sites on ZrP-600. The ZrP catalyst was easily regenerated by thermal treatment and showed stable activity upon its reuse. Preliminary calculations of the "minimum selling price" of HMF suggest that it is economically attractive to make this industrially-relevant chemical from FWB.