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Nuno M. R. Peres

Publications and source records attributed to Nuno M. R. Peres.

At least 19 recordsLinked to original sources

Exceptional point induced by hyperbolicity in an electrostatic spherical shell

Exceptional points (EPs) are non--Hermitian degeneracies at which both eigenvalues and eigenvectors coalesce, usually engineered through balanced gain and loss or non--reciprocity. In this work, we show that the radial electrostatic problem of an anisotropic core--shell nanoparticle realizes an EP without any of the alluded conditons. Written in the logarithmic radial coordinate, the problem is a Cauchy--Euler equation that maps onto a damped oscillator and, equivalently, onto a two-site Hatano--Nelson Hamiltonian, so that the non-Hermiticity is emulated in space rather than in time and the sole control parameter is the degree of dielectric anisotropy, $\varepsilon_t/\varepsilon_r$. The shell is passive, reciprocal, and lossless, yet it hosts an EP and a non--Hermitian phase transition governed by hyperbolicity alone. Beyond a hyperbolicity threshold the electric field inside the shell turns from monotonic decay into spatial oscillation, producing hotspots at intermediate radii which can be exploited to tailor fluorescence, strong coupling, sensing, or cloaking. More broadly, this establishes hyperbolic media as a platform to simulate non--Hermitian physics without gain, loss, or non--reciprocity.

cond-mat.mes-hall↗

Towards twisted, topological, and quantum graphene plasmonics

In this article, we analyze the quantum and topological properties of graphene-based plasmonic systems. We consider the following plasmonic materials: single-layer graphene, twisted bilayer graphene, and other graphene stackings, as well as the following architectures: graphene-based gratings, grids, chains of graphene disks, and the kagomé lattice.

cond-mat.mes-hall↗

Plasmon polariton assisted second-harmonic generation in graphene

In this paper we present a theoretical examination of second-harmonic generation (SHG) in a graphene monolayer integrated within an attenuated total internal reflection (ATR) configuration. By embedding graphene in this optical setup, we explore the enhancement in the nonlinear optical response, particularly focusing on the efficiency of SHG. Our analysis reveals that the excitation of surface plasmon-polaritons (SPPs) plays a central role in significantly boosting the efficiency of SHG. The unique electronic properties of graphene, combined with the resonant characteristics of SPPs, create a synergistic effect that amplifies the nonlinear optical signals. This enhancement is attributed to the strong field confinement and the resonant nature of SPPs, which effectively increase the interaction between the incident light and the graphene monolayer. Furthermore, we analyze the underlying mechanisms that govern this process, providing a comprehensive theoretical framework that elucidates the interplay between graphene's electronic structure and the optical fields. Our findings suggest that the ATR scheme not only facilitates the excitation of SPPs but also optimizes the conditions for SHG.

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Coupled electric dipole model for a Su-Schrieffer-Heeger chain of optically resonant coreshell nanoparticles

Coreshell nanoparticles can combine optical features of different materials in a single nanostructure, which makes them interesting for many applications from biomedicine to energy harvesting. On the other hand, periodic arrays of plasmonic nanoparticles can exhibit topological phenomena such as topological edge states. Here we study periodic chains of Si@Ag coreshell nanoparticles. For this task, we combine the hybridization of surface plasmonic modes in complex nanostructures with the coupled electric dipole formalism employed for modelling the scattering of light by periodic arrays of small plasmonic nanoparticles. We propose treating coreshell nanoparticle as several coupled electric dipoles instead of just one and show how this is a more appropriate framework to study arrays of coreshell nanoparticles, which allows to build a one-to-one connection between the resonant modes of the nanoparticles and the dispersion bands of the system. Within this formalism, we show that a Su-Schrieffer-Heeger (SSH) chain of coreshell Si@Ag nanoparticles host multiple topological edge states pinned at the resonant frequencies of the coreshell nanoparticles.

physics.optics↗

Nonlocal electrodynamics of two-dimensional anisotropic magneto-plasmons

We present a hydrodynamic model, grounded in Madelung's formalism, to describe collective electronic motion in anisotropic materials. This model incorporates nonlocal contributions from the Thomas-Fermi quantum pressure and quantum effects arising from the Bohm potential. We derive analytical expressions for the magnetoplasmon dispersion and nonlocal optical conductivity. To demonstrate the applicability of the model, we examine electrons in the conduction band of monolayer phosphorene, an exemplary anisotropic two-dimensional electron gas. The dispersion of plasmons derived from our hydrodynamic approach is closely aligned with that predicted by ab~initio calculations. Then, we use our model to analyze few-layer black phosphorus, whose measured infrared optical response is hyperbolic. Our results reveal that the incorporation of nonlocal and quantum effects in the optical conductivity prevents black phosphorus from supporting hyperbolic surface plasmon polaritons. We further demonstrate that the predicted wavefront generated by an electric dipole exhibits a significant difference between the local and nonlocal descriptions for the optical conductivity. This study underscores the necessity of moving beyond local approximations when investigating anisotropic systems capable of hosting strongly confined plasmon-polaritons.

cond-mat.mes-hall↗

Roadmap on Nonlocality in Photonic Materials and Metamaterials

Photonic technologies continue to drive the quest for new optical materials with unprecedented responses. A major frontier in this field is the exploration of nonlocal (spatially dispersive) materials, going beyond the local, wavevector-independent assumption traditionally made in optical material modeling. On one end, the growing interest in plasmonic, polaritonic and quantum materials has revealed naturally occurring nonlocalities, emphasizing the need for more accurate models to predict and design their optical responses. This has major implications also for topological, nonreciprocal, and time-varying systems based on these material platforms. Beyond natural materials, artificially structured materials--metamaterials and metasurfaces--can provide even stronger and engineered nonlocal effects, emerging from long-range interactions or multipolar effects. This is a rapidly expanding area in the field of photonic metamaterials, with open frontiers yet to be explored. In the case of metasurfaces, in particular, nonlocality engineering has become a powerful tool for designing strongly wavevector-dependent responses, enabling enhanced wavefront control, spatial compression, multifunctional devices, and wave-based computing. Furthermore, nonlocality and related concepts play a critical role in defining the ultimate limits of what is possible in optics, photonics, and wave physics. This Roadmap aims to survey the most exciting developments in nonlocal photonic materials, highlight new opportunities and open challenges, and chart new pathways that will drive this emerging field forward--toward new scientific discoveries and technological advancements.

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Broadband High-Performance Terahertz Polarizers by Nanoimprint Lithography for Advanced Applications

Terahertz polarizers are essential for advanced spectroscopic systems but face challenges like low transmission, short bandwidths and low extinction ratios. This study demonstrates the development of ultrabroadband THz polarizers using nanoimprint lithography, achieving high performance through double-wire-grid polarizer (DWGP) structures on cyclic olefin copolymer (COC) substrates. Compared to silicon-based alternatives, the polymer DWGPs demonstrated over twice the TM-polarized transmittance across the 0.1 - 25 THz range. The degree of polarization exceeded 98% in a 0.1-16 THz range, with a maximum extinction ratio above 65.4 dB at 4.2 THz. Simultaneous characterization of materials using THz time-domain spectroscopy (THz-TDS) and Fourier-transform infrared spectroscopy (FTIR) covered extended frequency ranges of 0.1 - 40 THz and 0.9 - 20 THz, respectively. Nanofabricated polymer DWGP revealed the superior optical properties, including enhanced TM transmittance and reduced TE leakage when compared to Si DWGP. Additionally, the fabricated polymer polarizers showcased cost-effectiveness, scalability, and durability, offering a sustainable alternative to conventional Si-based polarizers. The significant developments demonstrated in this study position polymer-based DWGPs as significant components for THz imaging, sensing, and wireless communication systems, paving the way for next-generation technologies.

physics.optics↗

Electrical Spectroscopy of Polaritonic Nanoresonators

One of the most captivating properties of polaritons is their capacity to confine light at the nanoscale. This confinement is even more extreme in two-dimensional (2D) materials. 2D polaritons have been investigated by optical measurements using an external photodetector. However, their effective spectrally resolved electrical detection via far-field excitation remains unexplored. This fact hinders their potential exploitation in crucial applications such as sensing molecules and gases, hyperspectral imaging and optical spectrometry, banking on their potential for integration with silicon technologies. Herein, we present the first electrical spectroscopy of polaritonic nanoresonators based on a high-quality 2D-material heterostructure, which serves at the same time as the photodetector and the polaritonic platform. We employ metallic nanorods to create hybrid nanoresonators within the hybrid plasmon-phonon polaritonic medium in the mid and long-wave infrared ranges. Subsequently, we electrically detect these resonators by near-field coupling to a graphene pn-junction. The nanoresonators simultaneously present a record of lateral confinement and high-quality factors of up to 200, exhibiting prominent peaks in the photocurrent spectrum, particularly at the underexplored lower reststrahlen band of hBN. We exploit the geometrical and gate tunability of these nanoresonators to investigate their impact on the photocurrent spectrum and the polaritonic's waveguided modes. This work opens a venue for studying this highly tunable and complex hybrid system, as well as for using it in compact platforms for sensing and photodetection applications.

physics.optics↗

Tunable exciton polaritons in band-gap engineered hexagonal boron nitride

We show that hexagonal boron nitride (hBN), a two-dimensional insulator, when subjected to an external superlattice potential forms a new paradigm for electrostatically tunable excitons in the near- and mid-ultraviolet (UV). The imposed potential has three consequences: (i) it renormalizes the effective mass tensor, leading to anisotropic effective masses; (ii) it renormalizes the band gap, eventually reducing it; (iii) it reduces the exciton binding energies. All these consequences depend on a single dimensionless parameter, which includes the product of strength of the external potential with its period. In addition to the excitonic energy levels, we compute the optical conductivity along two orthogonal directions, and from it the absorption spectrum. The results for the latter show that our system is able to mimic a grid polarizer. These characteristics make one-dimensional hBN superlattices a viable and unexplored platform for fine-tuned polaritonics in the UV to visible spectral range.

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Valley-selective confinement of excitons in transition metal dichalcogenides with inhomogeneous magnetic fields

Magnetized ferromagnetic disks or wires support strong inhomogeneous fields in their borders. Such magnetic fields create an effective potential, due to Zeeman and diamagnetic contributions, that can localize charge carriers. For the case of two-dimensional transition metal dichalcogenides, this potential can valley-localize excitons due to the Zeeman term, which breaks the valley symmetry. We show that the diamagnetic term is negligible when compared to the Zeeman term for monolayers of transition metal dichalcogenides. The latter is responsible for trapping excitons near the magnetized structure border with valley-dependent characteristics, in which, for one of the valleys, the exciton is confined inside the disk, while for the other, it is outside. This spatial valley separation of exciton can be probed by circularly polarized light, and moreover, we show that the inhomogeneous magnetic field magnitude, the dielectric environment, and the magnetized structure parameters can tailor the spatial separation of the exciton wavefunctions.

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Localized polariton states in a photonic crystal intercalated by a transition metal dichalcogenide monolayer

Beyond the extensively studied microcavity polaritons, which are coupled modes of semiconductor excitons and microcavity photons, nearly 2D semiconductors placed in a suitable environment can support spatially localized exciton-polariton modes. We demonstrate theoretically that two distinct types of such modes can exist in a photonic crystal with an embedded transition metal dichalcogenide (TMD) monolayer and derive an equation that determines their dispersion relations. The localized modes of two types occur in the zeroth- and first-order stop-bands of the crystal, respectively, and have substantially different properties. The latter type of the localized modes, which appear inside the light cone, can be described as a result of coupling of the TMD exciton and an optical Tamm state of the TMD-intercalated photonic crystal. We suggest an experiment for detecting these modes and simulate it numerically.

physics.optics↗

A critical analysis on the sensitivity enhancement of surface plasmon resonance sensors with graphene

The use of graphene in surface plasmon resonance sensors, covering a metallic (plasmonic) film, has a number of demonstrated advantages, such protecting the film against corrosion/oxidation and facilitating the introduction of functional groups for selective sensing. Recently, a number of works have claimed that few-layer graphene can also increase the sensitivity of the sensor. However, graphene was treated as an isotropic thin film, with an out-of-plane refractive index that is identical to the in-plane index. Here, we critically examine the role of single and few layers of graphene in the sensitivity enhancement of surface plasmon resonance sensors. Graphene is introduced over the metallic film via three different descriptions: as an atomic-thick two-dimensional sheet, as a thin effective isotropic material (same conductivity in the three coordinate directions), and as an non-isotropic layer (different conductivity in the perpendicular direction to the two-dimensional plane). We find that only the isotropic layer model, which is known to be incorrect for the optically modelling of graphene, provides sizeable sensitivity increases, while the other, more accurate, models lead to negligible contribution to the sensitivity.

cond-mat.mes-hall↗

Relaxing graphene plasmon excitation constraints through the use of an epsilon-near-zero substrate

Graphene plasmons have attracted significant attention due to their tunability, potentially long propagation lengths and ultracompact wavelengths. However, the latter characteristic imposes challenges to light-plasmon coupling in practical applications, generally requiring sophisticated coupling setups, extremely high doping levels and/or graphene nanostructuting close to the resolution limit of current lithography techniques. Here, we propose and theoretically demonstrate a method for alleviating such a technological strain through the use of a practical substrate whose low and negative dielectric function naturally enlarges the graphene polariton wavelength to more manageable levels. We consider silicon carbide (SiC), as it exhibits a dielectric function whose real part is between -1 and 0, while its imaginary part remains lower than 0.05, in the 951 to 970 cm$^{-1}$ mid-infrared spectral range. Our calculations show hybridization with the substrate's phonon polariton, resulting in a polariton wavelenth that is an order of magnitude longer than obtained with a silicon dioxide substrate, while the propagation length increases by the same amount.

physics.optics↗

Quantum Nanophotonics in Two-Dimensional Materials

The field of 2D materials-based nanophotonics has been growing at a rapid pace, triggered by the ability to design nanophotonic systems with in situ control, unprecedented degrees of freedom, and to build material heterostructures from bottom up with atomic precision. A wide palette of polaritonic classes have been identified, comprising ultra confined optical fields, even approaching characteristic length scales of a single atom. These advances have been a real boost for the emerging field of quantum nanophotonics, where the quantum mechanical nature of the electrons and-or polaritons and their interactions become relevant. Examples include, quantum nonlocal effects, ultrastrong light matter interactions, Cherenkov radiation, access to forbidden transitions, hydrodynamic effects, single plasmon nonlinearities, polaritonic quantization, topological effects etc. In addition to these intrinsic quantum nanophotonic phenomena, the 2D material system can also be used as a sensitive probe for the quantum properties of the material that carries the nanophotonics modes, or quantum materials in its vicinity. Here, polaritons act as a probe for otherwise invisible excitations, e.g. in superconductors, or as a new tool to monitor the existence of Berry curvature in topological materials and superlattice effects in twisted 2D materials.

physics.optics↗

Topological Graphene plasmons in a plasmonic realization of the Su-Schrieffer-Heeger Model

Graphene hybrids, made of thin insulators, graphene, and metals can support propagating acoustic plasmons (AGPs). The metal screening modifies the dispersion relation of usual graphene plasmons leading to slowly propagating plasmons, with record confinement of electromagnetic radiation. Here, we show that a graphene monolayer, covered by a thin dielectric material and an array of metallic nanorods can be used as a robust platform to emulate the Su-Schrieffer-Heeger model. We calculate the Zak's phase of the different plasmonic bands to characterise their topology. The system shows bulk-edge correspondence: strongly localized interface states are generated in the domain walls separating arrays in different topological phases. We find signatures of the nontrivial phase which can directly be probed by far-field mid-IR radiation, hence allowing a direct experimental confirmation of graphene topological plasmons. The robust field enhancement, highly localized nature of the interface states, and their gate-tuned frequencies expand the capabilities of AGP-based devices.

cond-mat.mes-hall↗

Highly Confined In-plane Exciton-Polaritons in Monolayer Semiconductors

2D materials support unique excitations of quasi-particles that consist of a material excitation and photons called polaritons. Especially interesting are in-plane propagating polaritons which can be confined to a single monolayer and carry large momentum. In this work, we report the existence of a new type of in-plane propagating polariton, supported on monolayer transition-metal-dicalcogonide (TMD) in the visible spectrum, which has not yet been observed. This 2D in-plane exciton-polariton (2DEP) is described by the coupling of an electromagnetic light field with the collective oscillations of the excitons supported by monolayer TMDs. We expose the specific experimental conditions required for the excitation of the 2DEP and show that these can be created if the TMD is encapsulated with hexagonal-boron-nitride (hBN) and cooled to cryogenic temperatures. In addition, we compare the properties of the 2DEPs with those of surface-plasmons-polaritons (SPPs) at the same spectral range, and find that the 2DEP exhibit over two orders-of-magnitude larger wavelength confinement. Finally, we propose two configurations for the possible experimental observation of 2DEPs.

physics.optics↗

Fresnel polarisation of infra-red radiation by elemental bismuth

We revisit the classical problem of electromagnetic wave refraction from a lossless dielectric to a lossy conductor, where both media are considered to be non-magnetic, linear, isotropic and homogeneous. We derive the Fresnel coefficients of the system and the Poynting vectors at the interface, in order to compute the reflectance and transmittance of the system. We use a particular parametrisation of the referred Fresnel coefficients so as to make a connection with the ones obtained for refraction by an interface between two lossless media. This analysis allows the discussion of an actual application, namely the Fresnel polarisation of infra-red radiation by elemental bismuth, based on the concept of pseudo Brewster's angle.

physics.optics↗

Anisotropic Stark shift, field-induced dissociation, and electroabsorption of excitons in phosphorene

We compute binding energies, Stark shifts, electric-field-induced dissociation rates, and the Franz-Keldysh effect for excitons in phosphorene in various dielectric surroundings. All three effects show a pronounced dependence on the direction of the in-plane electric field, with the dissociation rates in particular decreasing by several orders of magnitude upon rotating the electric field from the armchair to the zigzag axis. To better understand the numerical dissociation rates, we derive an analytical approximation to the anisotropic rates induced by weak electric fields, thereby generalizing the previously obtained result for isotropic two-dimensional semiconductors. This approximation is shown to be valid in the weak-field limit by comparing it to the exact rates. The anisotropy is also apparent in the large difference between armchair and zigzag components of the exciton polarizability tensor, which we compute for the five lowest lying states. As expected, we also find much more pronounced Stark shifts in either the armchair or zigzag direction, depending on the symmetry of the state in question. Finally, an isotropic interaction potential is shown to be an excellent approximation to a more accurate anisotropic interaction derived from the Poisson equation, confirming that the anisotropy of phosphorene is largely due to the direction dependence of the effective masses.

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