RESUMEN
Monitoring chemical levels is crucial for safeguarding both the environment and public health. Elevated levels of ammonia, for instance, can harm both humans and aquatic ecosystems, often indicating contamination from agriculture, industry, or sewage. Developing portable, high-resolution, and affordable methods for in situ monitoring of ammonia is thus imperative. Plasmonic sensors offer a promising solution, detecting ammonia by correlating changes in their optical response to the target analyte's concentration. While they are highly sensitive and can be fabricated in a variety of portable and user-friendly formats, some still require reagents or expensive optical equipment, which hinder their widespread adoption. Here, we present a self-assembled nanoplasmonic colorimetric sensor capable of directly detecting ammonia concentrations in aqueous matrices. The proposed sensor exploits the plasmonic resonance of the nanostructures to transduce changes in the chemical environment into alterations in color, offering a label-free method for real-time analysis. The sensor is fabricated using a self-assembling technique compatible with low-cost mass production based on aluminum and aluminum oxide, ensuring affordability and avoiding the use of other toxic chemicals. We developed a model to predict ammonia concentrations based on visible color change of the sensor, achieving a detection limit of 8.5 ppm. Furthermore, to address the need for on-site detection, we integrated smartphone technology for real-time color change analysis, eliminating the need for expensive, bulky optical instruments. Indeed, our approach offers a cost-effective, portable, and user-friendly solution for ammonia detection in water without the need for chemical reagents or spectrometers, making it ideal for field applications. Interestingly, this platform extends its applicability beyond ammonia detection, enabling the monitoring of various chemicals using a smartphone, without the need for any additional costly equipment.
RESUMEN
The accurate detection, classification, and separation of chiral molecules are pivotal for advancing pharmaceutical and biomolecular innovations. Engineered chiral light presents a promising avenue to enhance the interaction between light and matter, offering a noninvasive, high-resolution, and cost-effective method for distinguishing enantiomers. Here, we present a nanostructured platform for surface-enhanced infrared absorption-induced vibrational circular dichroism (VCD) based on an achiral plasmonic system. This platform enables precise measurement, differentiation, and quantification of enantiomeric mixtures, including concentration and enantiomeric excess determination. Our experimental results exhibit a 13 orders of magnitude higher detection sensitivity for chiral enantiomers compared to conventional VCD spectroscopic techniques, accounting for respective path lengths and concentrations. The tunable spectral characteristics of this achiral plasmonic system facilitate the detection of a diverse range of chiral compounds. The platform's simplicity, tunability, and exceptional sensitivity holds remarkable potential for enantiomer classification in drug design, pharmaceuticals, and biological applications.
RESUMEN
All present commercial colors are based on pigments. While such traditional pigment-based colorants offer a commercial platform for large-volume and angle insensitiveness, they are limited by their instability in atmosphere, color fading, and severe environmental toxicity. Commercial exploitation of artificial structural coloration has fallen short due to the lack of design ideas and impractical nanofabrication techniques. Here, we present a self-assembled subwavelength plasmonic cavity that overcomes these challenges while offering a tailorable platform for rendering angle and polarization-independent vivid structural colors. Fabricated through large-scale techniques, we produce stand-alone paints ready to be used on any substrate. The platform offers full coloration with a single layer of pigment, surface density of 0.4 g/m2, making it the lightest paint in the world.
RESUMEN
The tunable angle-selective transparency of hyperbolic metamaterials consisting of various multilayers of Dirac semimetal and dielectric materials are theoretically and numerically studied in the terahertz range. Three stack configurations are considered: alternating, sandwiched, and disordered. It is found that the proposed structures exhibit strong optical angular selectivity induced by photonic topological transition for transverse magnetic waves. Interestingly, the topological transition frequency can be flexibly modulated by changing the Fermi energy, temperature, and the releasing time of the Dirac semimetal, as well as the thickness ratio of the dielectric and semimetal layers. It is also noticed that the angular optical transparency properties are independent of the order of the proposed structure even in alternating/disordered/random configurations if the total thickness ratio of the semimetal to dielectric are the same, which makes the properties particularly easy to realize experimentally. The proposed hyperbolic metamaterial structures present a promising opportunity for wavefront engineering, offering crucial properties for applications in private screens, optical detectors, and light manipulation.
RESUMEN
Nanostructured plasmonic materials can lead to the extremely compact pixels and color filters needed for next-generation displays by interacting with light at fundamentally small length scales. However, previous demonstrations suffer from severe angle sensitivity, lack of saturated color, and absence of black/gray states and/or are impractical to integrate with actively addressed electronics. Here, we report a vivid self-assembled nanostructured system which overcomes these challenges via the multidimensional hybridization of plasmonic resonances. By exploiting the thin-film growth mechanisms of aluminum during ultrahigh vacuum physical vapor deposition, dense arrays of particles are created in near-field proximity to a mirror. The sub-10-nm gaps between adjacent particles and mirror lead to strong multidimensional coupling of localized plasmonic modes, resulting in a singular resonance with negligible angular dispersion and â¼98% absorption of incident light at a desired wavelength. The process is compatible with arbitrarily structured substrates and can produce wafer-scale, diffusive, angle-independent, and flexible plasmonic materials. We then demonstrate the unique capabilities of the strongly coupled plasmonic system via integration with an actively addressed reflective liquid crystal display with control over black states. The hybrid display is readily programmed to display images and video.
RESUMEN
We demonstrate a reflective light modulator, a dynamic Salisbury screen where modulation of light is achieved by moving a thin metamaterial absorber to control its interaction with the standing wave formed by the incident wave and its reflection on a mirror. Electrostatic actuation of the plasmonic metamaterial absorber's position leads to a dynamic change of the Salisbury screen's spectral response and 50% modulation of the reflected light intensity in the near infrared part of the spectrum. The proposed approach can also be used with other metasurfaces to control the changes they impose on the polarization, intensity, phase, spectrum and directional distribution of reflected light.
RESUMEN
While metamaterials offer engineered static optical properties, future artificial media with dynamic random-access control over shape and position of meta-molecules will provide arbitrary control of light propagation. The simplest example of such a reconfigurable metamaterial is a nanowire grid metasurface with subwavelength wire spacing. Recently we demonstrated computationally that such a metadevice with individually controlled wire positions could be used as dynamic diffraction grating, beam steering module and tunable focusing element. Here we report on the nanomembrane realization of such a nanowire grid metasurface constructed from individually addressable plasmonic chevron nanowires with a 230 nm × 100 nm cross-section, which consist of gold and silicon nitride. The active structure of the metadevice consists of 15 nanowires each 18 µm long and is fabricated by a combination of electron beam lithography and ion beam milling. It is packaged as a microchip device where the nanowires can be individually actuated by control currents via differential thermal expansion.
RESUMEN
Effectively continuous control over propagation of a beam of light requires light modulation with pixelation that is smaller than the optical wavelength. Here we propose a spatial intensity modulator with sub-wavelength resolution in one dimension. The metadevice combines recent advances in reconfigurable nanomembrane metamaterials and coherent all-optical control of metasurfaces. It uses nanomechanical actuation of metasurface absorber strips placed near a mirror in order to control their interaction with light from perfect absorption to negligible loss, promising a path towards dynamic diffraction and focusing of light as well as holography without unwanted diffraction artefacts.
RESUMEN
Dynamic control over optical wavefronts enables focusing, diffraction and redirection of light on demand, however, sub-wavelength resolution is required to avoid unwanted diffracted beams that are present in commercial spatial light modulators. Here we propose a realistic metadevice that dynamically controls the optical phase of reflected beams with sub-wavelength pixelation in one dimension. Based on reconfigurable metamaterials and nanomembrane technology, it consists of individually moveable metallic nanowire actuators that control the phase of reflected light by modulating the optical path length. We demonstrate that the metadevice can provide on-demand optical wavefront shaping functionalities of diffraction gratings, beam splitters, phase-gradient metasurfaces, cylindrical mirrors and mirror arrays - with variable focal distance and numerical aperture - without unwanted diffraction.