Juan M. Sanz

Rhodium Nanoparticles for Ultraviolet Plasmonics

The nonoxidizing catalytic noble metal rhodium is introduced for ultraviolet plasmonics. Planar tripods of 8 nm Rh nanoparticles, synthesized by a modified polyol reduction method, have a calculated local surface plasmon resonance near 330 nm. By attaching p-aminothiophenol, local field-enhanced Raman spectra and accelerated photodamage were observed under near-resonant ultraviolet illumination, while charge transfer simultaneously increased fluorescence for up to 13 min. The combined local field enhancement and charge transfer demonstrate essential steps toward plasmonically enhanced ultraviolet photocatalysis.

How an oxide shell affects the ultraviolet plasmonic behavior of Ga, Mg, and Al nanostructures.

The ultraviolet (UV) range presents new challenges for plasmonics, with interesting applications ranging from engineering to biology. In previous research, gallium, aluminum, and magnesium were found to be very promising UV plasmonic metals. However, a native oxide shell surrounds nanostructures of these metals that affects their plasmonic response. Here, through a nanoparticle-oxide core-shell model, we present a detailed electromagnetic analysis of how oxidation alters the UV-plasmonic response of spherical or hemisphere-on-substrate nanostructures made of those metals by analyzing the spectral evolution of two parameters: the absorption efficiency (far-field analysis) and the enhancement of the local intensity averaged over the nanoparticle surface (near-field analysis).

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%.

Polar decomposition of the Mueller matrix: a polarimetric rule of thumb for square-profile surface structure recognition

In this research, the polar decomposition (PD) method is applied to experimental Mueller matrices (MMs) measured on two-dimensional microstructured surfaces. Polarization information is expressed through a set of parameters of easier physical interpretation. It is shown that evaluating the first derivative of the retardation parameter, δ, a clear indication of the presence of defects either built on or dug in the scattering flat surface (a silicon wafer in our case) can be obtained. Although the rule of thumb thus obtained is established through PD, it can be easily implemented on conventional surface polarimetry. These results constitute an example of the capabilities of the PD approach to MM analysis, and show a direct application in surface characterization.

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.

Nanoscopic surface inspection by analyzing the linear polarization degree of the scattered light

We present an optical method for the nanoscopic inspection of surfaces. The method is based on the spectral and polarization analysis of the light scattered by a probe nanoparticle close to the inspected surface. We explore the sensitivity to changes either in the probe-surface distance or in the refractive index of the surface.

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.

Frequency shift between near- and far-field scattering resonances in dielectric particles.

The near-field electromagnetic scattering intensity resonances are redshifted in frequency with respect to their far-field counterparts. We derive simple, approximate, analytical formulas for this shift in the case of a plane wave interacting with a dielectric sphere. Numerical results comparing the approximate formulas to the numerically exact solutions show that the two are in good agreement. We also consider the Rayleigh limit of the formulas to gain more insight into the phenomenon.

Recent advances in metals for plasmonics applications in the UV range

Plasmonics in the UV-range constitutes a new focus of research due to new challenges arising in fields such as biology, chemistry or spectroscopy. Very recent studies point out gallium and rhodium as good candidates for these purposes because of their low oxidation tendency and at the same time, having a good plasmonic response in the UV and excellent photocatalytic properties. Here we present an overview of the current state of UV-plasmonics with our latest findings in the plasmonic activity of materials like gallium and rhodium.