Ángela I. Barreda

Size-tunable rhodium nanostructures for wavelength-tunable ultraviolet plasmonics

Polydisperse rhodium nanoparticles have recently shown promise for ultraviolet (UV) plasmonics, but controlling the size and morphology of metal nanoparticles is essential for tuning surface plasmon resonances. Here we report the use of slow-injection polyol methods to synthesize monodisperse Rh nanocubes with unprecedentedly large sizes and slightly concave faces. The associated local surface plasmon resonances (LSPRs) red-shifted with increasing sizes in the UV region from deep UV to around 400 nm, consistent with numerical simulations. UV illumination of p-aminothiophenol attached to the Rh nanocubes generated surface-enhanced Raman spectra and accelerated photo-decomposition, and these enhancements were largest for nanocubes whose LSPR was resonant with the UV laser. The lack of a native oxide coating, the precise control of nanocube size and morphology demonstrated here, and the ability to tune the surface plasmon resonance from the deep UV to near UV spectral region, make rhodium a compelling choice for UV plasmonic applications.

Influence of pollutants in the magneto-dielectric response of silicon nanoparticles

The influence of the degree of purity of a silicon nanoparticle on its resonances, either electric or magnetic, is assessed by using Mie theory as well as finite-element simulations. In particular, it is shown that the main effect of the increase of absorption due to the pollutants is observed in the magnetic resonances. Concerning Kerkers conditions for the directionality of the scattering [J. Opt. Soc. Am.73, 765 (1983)], it is found that both are strongly shifted when the materials purity is varied. Resistive losses confirm the quenching of magnetic resonances, showing that the region of influence in the magnetic dipole resonance is much larger than in the electric one, although it has been found that losses are not critical for silicon content over 99.50%.

Electromagnetic polarization-controlled perfect switching effect with high-refractive-index dimers and the beam-splitter configuration.

Sub-wavelength particles made from high-index dielectrics, either individual or as ensembles, are ideal candidates for multifunctional elements in optical devices. Their directionality effects are traditionally analysed through forward and backward measurements, even if these directions are not convenient for in-plane scattering practical purposes. Here we present unambiguous experimental evidence in the microwave range that for a dimer of HRI spherical particles, a perfect switching effect is observed out of those directions as a consequence of the mutual particle electric/magnetic interaction. The binary state depends on the excitation polarization. Its analysis is performed through the linear polarization degree of scattered radiation at a detection direction perpendicular to the incident direction: the beam-splitter configuration. The scaling property of Maxwells equations allows the generalization of our results to other frequency ranges and dimension scales, for instance, the visible and the nanometric scale.

Using linear polarization for sensing and sizing dielectric nanoparticles.

The spectral evolution of the degree of linear polarization (PL) at a scattering angle of 90° is studied numerically for high refractive index (HRI) dielectric spherical nanoparticles. The behaviour of PL(90°) is analysed as a function of the refractive index of the surrounding medium and the particle radius, and it is compared with the more conventional extinction efficiency parameter (Qext), usually used for sensing applications. We focus on the spectral region where both electric and magnetic resonances of order not higher than two are located for various semiconductor materials with low absorption. Although both Qext and PL(90°) are identifiers of the refractive index of the surrounding medium, the spectral of PL(90°) has only a small, linear dependence on nanoparticle size R. This weak dependence makes it experimentally feasible to perform real-time retrievals of both the refractive index of the external medium and the NP size R.

Polarimetric response of magnetodielectric core–shell nanoparticles: an analysis of scattering directionality and sensing

The influence of increasing the core size of Ag-Si core-shell nanoparticles has been investigated by using the values of the linear polarization degree at a right-angle scattering configuration, [Formula: see text]. Changes in dipolar resonances and scattering directionality conditions as a function of the core radius (R int) for a fixed shell size ([Formula: see text] nm) have been analysed. An empirical formula to obtain the ratio [Formula: see text] by monitoring the influence of the magnetic dipolar resonance in [Formula: see text] has been found. The effect of the refractive index of the surrounding medium, m med, in the zero backward and almost-zero forward scattering conditions has also been studied. We have weighed up the sensitivity of [Formula: see text] to m med. It has been demonstrated that multipolar contributions strongly influence [Formula: see text]. This influence can be used as a fast m med estimate. In all cases, the results show that the bigger the cores, the higher the sensitivity to m med.

Light guiding and switching using eccentric core-shell geometries

High Refractive Index (HRI) dielectric nanoparticles have been proposed as an alternative to metallic ones due to their low absorption and magnetodielectric response in the VIS and NIR ranges. For the latter, important scattering directionality effects can be obtained. Also, systems constituted by dimers of HRI dielectric nanoparticles have shown to produce switching effects by playing with the polarization, frequency or intensity of the incident radiation. Here, we show that scattering directionality effects can be achieved with a single eccentric metallo-HRI dielectric core-shell nanoparticle. As an example, the effect of the metallic core displacements for a single Ag-Si core-shell nanoparticle has been analyzed. We report rotation of the main scattering lobe either clockwise or counterclockwise depending on the polarization of the incident radiation leading to new scattering configurations for switching purposes. Also, the efficiency of the scattering directionality can be enhanced. Finally, chains of these scattering units have shown good radiation guiding effects, and for 1D periodic arrays, redirection of diffracted intensity can be observed as a consequence of blazing effects. The proposed scattering units constitute new blocks for building systems for optical communications, solar energy harvesting devices and light guiding at the nanoscale level.

On the scattering directionality of a dielectric particle dimer of High Refractive Index

Low-losses and directionality effects exhibited by High Refractive Index Dielectric particles make them attractive for applications where radiation direction control is relevant. For instance, isolated metallo-dielectric core-shell particles or aggregates (dimers) of High Refractive Index Dielectric particles have been proposed for building operational switching devices. Also, the possibility of using isolated High Refractive Index Dielectric particles for optimizing solar cells performance has been explored. Here, we present experimental evidence in the microwave range, that a High Refractive Index Dielectric dimer of spherical particles is more efficient for redirecting the incident radiation in the forward direction than the isolated case. In fact, we report two spectral regions in the dipolar spectral range where the incident intensity is mostly scattered in the forward direction. They correspond to the Zero-Backward condition (also observed for isolated particles) and to a new condition, denoted as “near Zero-Backward” condition, which comes from the interaction effects between the particles. The proposed configuration has implications in solar energy harvesting devices and in radiation guiding.

Polarimetric techniques for determining morphology and optical features of high refractive index dielectric nanoparticle size

The spectral evolution of the degree of linear polarization (PL) at a scattering angle of 90° is studied numerically for high refractive index (HRI) dielectric spherical nanoparticles. The behaviour of PL(90°) is analyzed as a function of the refractive index of the surrounding medium and the particle radius. We focus on the spectral region where both electric and magnetic resonances of order not higher than two are located for various semiconductor materials with low absorption. The spectral behavior of PL(90°) has only a small, linear dependence on nanoparticle size R. This weak dependence makes it experimentally feasible to perform real-time retrievals of both the refractive index of the external medium and the NP size R. From an industrial point of view, pure materials are nonrealistic, since they can only be provided under certain conditions. For this reason, we also study the effect of contaminants on the resonances of silicon NPs by considering the spectral evolution of PL(90°).

Spectral response of dielectric nano-antennas in the far- and near-field regimes

Recent studies show that the spectral behaviour of localized surface plasmon resonances (LPSRs) in metallic nanoparticles suffer from both a redshift and a broadening in the transition from the far- to the near-field regimes. An interpretation of this effect was given in terms of the evanescent and propagating components of the angular spectrum representation of the radiated field. Due to the increasing interest awakened by magnetodielectric materials as a both low-loss material option for nanotechnology applications, and also for their particular scattering properties, here we study the spectral response of a magnetodielectric nanoparticle as a basic element of a dielectric nano-antenna. This study is made by analyzing the changes suffered by the scattered electromagnetic field when propagating from the surface of this dielectric nanostructure to the far-zone in terms of propagating and evanescent plane wave components of the radiated fields.

Plasmonics in the UV range with Rhodium nanocubes

Plasmonics in the UV-range constitutes a new challenge due to the increasing demand to detect, identify and destroy biological toxins, enhance biological imaging, and characterize semiconductor devices at the nanometer scale. Silver and aluminum have an efficient plasmonic performance in the near UV region, but oxidation reduces its performance in this range. Recent studies point out rhodium as one of the most promising metals for this purpose: it has a good plasmonic response in the UV and, as gold in the visible, it presents a low tendency to oxidation. Moreover, its easy fabrication through chemical means and its potential for photocatalytic applications, makes this material very attractive for building plasmonic tools in the UV. In this work, we will show an overview of our recent collaborative research with rhodium nanocubes (NC) for Plasmonics in the UV.