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Eduardo J. C. Dias

Publications and source records attributed to Eduardo J. C. Dias.

18 recordsLinked to original sources

Active steering of cathodoluminescence through a generalized Smith-Purcell effect

Optical metasurfaces can shape the near fields of energetic electrons, enabling Smith-Purcell (SP) emission. We introduce a generalized SP effect relying on finite periodic arrays whose elements possess individually tunable polarizabilities, allowing us to explore higher-order SP radiation. By controlling the amplitude and phase of each of the elements, we show through rigorous theory the ability to create an SP steering device. In particular, we explore the active tuning capabilities of doped graphene, and thermally driven phase-change materials, which we compare with standard passive plasmonic structures made of gold and silver. Our results establish programmable electron-driven light sources and spectroscopic probes spanning the terahertz-to-visible range, advancing tunable metasurfaces for next-generation electron-photon technologies.

physics.optics↗

Wave-mixing cathodoluminescence microscopy of low-frequency excitations

Nonlinear optical phenomena such as parametric amplification and frequency conversion are typically driven by external optical fields. Free electrons can also act as electromagnetic sources, offering unmatched spatial precision. Combining optical and electron-induced fields via the nonlinear response of material structures therefore holds potential for revealing new physical phenomena and enabling disruptive applications. Here, we theoretically investigate wave mixing between external light and the evanescent fields of free electrons, giving rise to inelastic photon scattering mediated by the second-order nonlinear response of a specimen. Specifically, an incident photon may be blue- or red-shifted, while the passing electron correspondingly loses or gains energy. These processes are strongly enhanced when the frequency shift matches an optical resonance of the specimen. We present a general theoretical framework to quantify the photon conversion probability and demonstrate its application by revealing far-infrared vibrational fingerprints of retinal using only visible light. Beyond its fundamental interest, this phenomenon offers a practical approach for spatially mapping low-frequency excitations with nanometer resolution using visible photon energies and existing electron microscopes.

cond-mat.mes-hall↗

Roadmap for Photonics with 2D Materials

Triggered by the development of exfoliation and the identification of a wide range of extraordinary physical properties in self-standing films consisting of one or few atomic layers, two-dimensional (2D) materials such as graphene, transition metal dichalcogenides (TMDs), and other van der Waals (vdW) crystals currently constitute a wide research field protruding in multiple directions in combination with layer stacking and twisting, nanofabrication, surface-science methods, and integration into nanostructured environments. Photonics encompasses a multidisciplinary collection of those directions, where 2D materials contribute with polaritons of unique characteristics such as strong spatial confinement, large optical-field enhancement, long lifetimes, high sensitivity to external stimuli (e.g., electric and magnetic fields, heating, and strain), a broad spectral range from the far infrared to the ultraviolet, and hybridization with spin and momentum textures of electronic band structures. The explosion of photonics with 2D materials as a vibrant research area is producing breakthroughs, including the discovery and design of new materials and metasurfaces with unprecedented properties as well as applications in integrated photonics, light emission, optical sensing, and exciting prospects for applications in quantum information, and nanoscale thermal transport. This Roadmap summarizes the state of the art in the field, identifies challenges and opportunities, and discusses future goals and how to meet them through a wide collection of topical sections prepared by leading practitioners.

cond-mat.mtrl-sci↗

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.

cond-mat.mes-hall↗

Prospects to bypass nonlocal phenomena in metals using phonon-polaritons

Electromagnetic design relies on an accurate understanding of light-matter interactions, yet often overlooks electronic length scales. Under extreme confinement, this omission can lead to nonclassical effects, such as nonlocal response. Here, we use mid-infrared phonon-polaritons in hexagonal boron nitride (hBN) screened by monocrystalline gold flakes to push the limits of nanolight confinement unobstructed by nonlocal phenomena, even when the polariton phase velocity approaches the Fermi velocities of electrons in gold. We employ near-field imaging to probe polaritons in nanometre-thin crystals of hBN on gold and extract their complex propagation constant, observing effective indices exceeding 90. We further show the importance of sample characterisation by revealing a thin low-index interfacial layer naturally forming on monocrystalline gold. Our experiments address a fundamental limitation posed by nonlocal effects in van der Waals heterostructures and outline a pathway to bypass their impact in high-confinement regimes.

physics.optics↗

Free-electron coupling to surface polaritons mediated by small scatterers

The ability of surface polaritons (SPs) to enhance and manipulate light fields down to deep-subwavelength length scales enables applications in optical sensing and nonlinear optics at the nanoscale. However, the wavelength mismatch between light and SPs prevents direct optical excitation of surface-bound modes, thereby limiting the widespread development of SP-based photonics. Free electrons are a natural choice to directly excite strongly confined SPs because they can supply field components of high momentum at designated positions with subnanometer precision. Here, we theoretically explore free-electron--SP coupling mediated by small scatterers and show that low-energy electrons can efficiently excite surface modes with a maximum probability reached at an optimum surface--scatterer distance. By aligning the electron beam with a periodic array of scatterers placed near a polariton-supporting interface, in-plane Smith--Purcell emission results in the excitation of surface modes along well-defined directions. Our results support using scattering elements to excite SPs with low-energy electrons.

cond-mat.mes-hall↗

Generation and control of localized terahertz fields in photoemitted electron plasmas

Dense micron-sized electron plasmas, such as those generated upon irradiation of nanostructured metallic surfaces by intense femtosecond laser pulses, constitute a rich playground to study light-matter interactions, many-body phenomena, and out-of-equilibrium charge dynamics. Besides their fundamental interest, laser-induced plasmas hold potential for the generation of localized terahertz radiation pulses. However, the underlying mechanisms ruling the formation and evolution of these plasmas is not yet well understood. Here, we develop a comprehensive microscopic theory to predictably describe the spatiotemporal dynamics of laser-pulse-induced plasmas. Through detailed analysis of electron emission, metal screening, and plasma cloud interactions, we investigate the spatial, temporal, and spectral characteristics of the so-generated terahertz fields, which can be extensively controlled through the metal morphology and the illumination conditions. We further describe the interaction with femtosecond electron beams to explain recent ultrafast electron microscopy experiments, whereby the position and temporal dependence of the observed electron acceleration permits assessing the associated terahertz field. Besides its potential application to the design of low-frequency light sources, our work contributes with fundamental insight on the generation and dynamics of micron-scale electron plasmas and their interaction with ultrafast electron pulses.

cond-mat.mes-hall↗

$μ$eV electron spectromicroscopy using free-space light

The synergy between free electrons and light has recently been leveraged to reach an impressive degree of simultaneous spatial and spectral resolution, enabling applications in microscopy and quantum optics. However, the required combination of electron optics and light injection into the spectrally narrow modes of arbitrary specimens remains a challenge. Here, we demonstrate microelectronvolt spectral resolution in the nanoscale mapping of photonic modes with quality factors as high as 10$^4$. We rely on mode-matching of a tightly focused laser beam to whispering gallery modes to achieve a 10$^8$-fold increase in light-electron coupling efficiency. By adapting the shape and size of free-space optical beams to address specific physical questions, our approach allows us to interrogate any type of photonic structure with unprecedented spectral and spatial detail

cond-mat.mes-hall↗

Charge dynamics electron microscopy: nanoscale imaging of femtosecond plasma dynamics

Understanding and actively controlling the spatio-temporal dynamics of non-equilibrium electron clouds is fundamental for the design of light and electron sources, novel high-power electronic devices, and plasma-based applications. However, electron clouds evolve in a complex collective fashion on nanometer and femtosecond scales, producing electromagnetic screening that renders them inaccessible to existing optical probes. Here, we solve the long-standing challenge of characterizing the evolution of electron clouds generated upon irradiation of metallic structures using an ultrafast transmission electron microscope to record the charged plasma dynamics. Our approach to charge dynamics electron microscopy (CDEM) is based on the simultaneous detection of electron-beam acceleration and broadening with nanometer/femtosecond resolution. By combining experimental results with comprehensive microscopic theory, we provide deep understanding of this highly out-of-equilibrium regime, including previously inaccessible intricate microscopic mechanisms of electron emission, screening by the metal, and collective cloud dynamics. Beyond the present specific demonstration, the here introduced CDEM technique grants us access to a wide range of non-equilibrium electrodynamic phenomena involving the ultrafast evolution of bound and free charges on the nanoscale.

physics.app-ph↗

Ultrafast Electron Microscopy of Nanoscale Charge Dynamics in Semiconductors

The ultrafast dynamics of charge carriers in solids plays a pivotal role in emerging optoelectronics, photonics, energy harvesting, and quantum technology applications. However, the investigation and direct visualization of such non-equilibrium transport phenomena remains as a long-standing challenge, owing to the nanometer-femtosecond spatio-temporal scales at which the charge carriers evolve. Here, we propose and demonstrate a novel interaction mechanism enabling nanoscale imaging of the femtosecond dynamics of charge carriers in solids. This imaging modality, which we name charge dynamics electron microscopy (CDEM), exploits the strong interaction between terahertz (THz) electromagnetic near fields produced by the moving charges and synchronized free-electron pulses in an ultrafast scanning transmission electron microscope. The measured free-electron energy at different spatio-temporal coordinates allows us to directly retrieve the THz near-field amplitude and phase, from which we reconstruct movies of the generated charges by comparison with microscopic theory. The introduced CDEM technique thus allows us to investigate previously inaccessible spatio-temporal regimes of charge dynamics in solids, for example revealing new insight into the photo-Dember effect, showing oscillations of photo-generated electron-hole distributions inside a semiconductor. Our work lays the foundation for exploring a wide range of previously inaccessible charge-transport phenomena in condensed matter using ultrafast electron microscopy.

cond-mat.mes-hall↗

High-harmonic generation enhancement with graphene heterostructures

We investigate high-harmonic generation in graphene heterostructures consisting of metallic nanoribbons separated from a graphene sheet by either a few-nanometer layer of aluminum oxide or an atomic monolayer of hexagonal boron nitride. The nanoribbons amplify the near-field at the graphene layer relative to the externally applied pumping, thus allowing us to observe third- and fifth-harmonic generation in the carbon monolayer at modest pump powers in the mid-infrared. We study the dependence of the nonlinear signals on the ribbon width and spacer thickness, as well as pump power and polarization, and demonstrate enhancement factors relative to bare graphene reaching 1600 and 4100 for third- and fifth-harmonic generation, respectively. Our work supports the use of graphene heterostructures to selectively enhance specific nonlinear processes of interest, an essential capability for the design of nanoscale nonlinear devices.

cond-mat.mes-hall↗

Complete Excitation of Discrete Quantum Systems by Single Free Electrons

We reveal a wealth of nonlinear and recoil effects in the interaction between individual low-energy electrons and samples comprising a discrete number of states. Adopting a quantum theoretical description of combined free-electron and two-level systems, we find a maximum achievable excitation probability of $100\%$, which requires specific conditions relating to the coupling strength and the transition symmetry, as we illustrate through calculations for dipolar and quadrupolar modes. Strong recoil effects are observed when the kinetic energy of the probe lies close to the transition threshold, although the associated probability remains independent of the electron wave function even when fully accounting for nonlinear interactions with arbitrarily complex multilevel samples. Our work reveals the potential of free electrons to control localized excitations and delineates the boundaries of such control.

quant-ph↗

Ultrafast Momentum-Resolved Probing of Plasmon Thermal Dynamics with Free Electrons

Current advances in ultrafast electron microscopy make it possible to combine optical pumping of a nanostructure and electron beam probing with subångstrom and femtosecond spatiotemporal resolution. We present a theory predicting that this technique can reveal a rich out-of-equilibrium dynamics of plasmon excitations in graphene and graphite samples. In a disruptive departure from the traditional probing of nanoscale excitations based on the identification of spectral features in the transmitted electrons, we show that measurement of angle-resolved, energy-integrated inelastic electron scattering can trace the temporal evolution of plasmons in these structures and provide momentum-resolved mode identification, thus avoiding the need for highly-monochromatic electron beams and the use of electron spectrometers. This previously unexplored approach to study the ultrafast dynamics of optical excitations can be of interest to understand and manipulate polaritons in 2D semiconductors and other materials exhibiting a strong thermo-optical response.

cond-mat.mtrl-sci↗

Complete Coupling of Focused Light to Surface Polaritons

Surface polaritons display short wavelengths compared to propagating light, thus enabling large spatial concentration and enhancement of electromagnetic energy. However, this wavelength mismatch is generally accompanied by poor light-to-polaritons coupling that limits potential applications in areas such as optical sensing and optoelectronics. Here, we address this problem by demonstrating that a small scatterer placed at a suitable distance from a planar surface can produce complete coupling of a focused light beam to surface polaritons. We present rigorous theoretical results for light coupling to plasmons in silver films and graphene, as well as phonon polaritons in hexagonal boron nitride films. We further formulate detailed general prescriptions on the beam profile and particle response that are required to achieve maximum coupling, which we supplement by analytical calculations for dipolar scatterers and finite-size particles. Our results open a practical route to circumvent the long-standing photon-polariton wavelength mismatch problem in nanophotonics.

physics.optics↗

Fundamental Limits to the Coupling between Light and 2D Polaritons by Small Scatterers

Polaritonic modes in two-dimensional van der Waals materials display short in-plane wavelengths compared with light in free space. As interesting as this may look from both fundamental and applied viewpoints, such large confinement is accompanied by poor in/out optical coupling, which severely limits the application of polaritons in practical devices. Here, we quantify the coupling strength between light and 2D polaritons in both homogeneous and anisotropic films using accurate rigorous analytical methods. In particular, we obtain universal expressions for the cross sections associated with photon-polariton coupling by point and line defects, as well as with polariton extinction and scattering processes. Additionally, we find closed-form constraints that limit the maximum possible values of these cross sections. Specifically, the maximum photon-to-plasmon conversion efficiency in graphene is $\sim10^{-6}$ and $\sim10^{-4}$ for point and line scatterers sitting at its surface, respectively, when the plasmon and photon energies are comparable in magnitude. We further show that Mie resonators placed at an optimum distance from the film can boost light-to-polariton coupling to order unity. Our results bear fundamental interest for the development of 2D polaritonics and the design of applications based on these excitations.

cond-mat.mes-hall↗

Probing Nonlocal Effects in Metals with Graphene Plasmons

In this paper we analyze the effects of nonlocality on the optical properties of a system consisting of a thin metallic film separated from a graphene sheet by a hexagonal boron nitride (hBN) layer. We show that nonlocal effects in the metal have a strong impact on the spectrum of the surface plasmon-polaritons on graphene. If the graphene sheet is shaped into a grating, we show that the extinction curves can be used to shed light on the importance of nonlocal effects in metals. Therefore, graphene surface plasmons emerge as a tool for probing nonlocal effects in metallic nanostructures, including thin metallic films. As a byproduct of our study, we show that nonlocal effects lead to smaller losses for the graphene plasmons than what is predicted by a local calculation. We show that these effects can be very well mimicked using a local theory with an effective spacer thickness larger than its actual value.

cond-mat.mes-hall↗

Probing the Ultimate Plasmon Confinement Limits with a Van der Waals heterostructure

The ability to confine light into tiny spatial dimensions is important for applications such as microscopy, sensing and nanoscale lasers. While plasmons offer an appealing avenue to confine light, Landau damping in metals imposes a trade-off between optical field confinement and losses. We show that a graphene-insulator-metal heterostructure can overcome that trade-off, and demonstrate plasmon confinement down to the ultimate limit of the lengthscale of one atom. This is achieved by far-field excitation of plasmon modes squeezed into an atomically thin hexagonal boron nitride dielectric h-BN spacer between graphene and metal rods. A theoretical model which takes into account the non-local optical response of both graphene and metal is used to describe the results. These ultra-confined plasmonic modes, addressed with far-field light excitation, enables a route to new regimes of ultra-strong light-matter interactions.

cond-mat.mes-hall↗

Controlling spoof plasmons in a metal grating using graphene surface plasmons

Spoof plasmons mimic noble metal plasmons. The equivalent of the plasma frequency is an energy scale imposed by the geometry of the metal grating upon which they propagate. In this paper we show that the dispersion of spoof plasmons in the THz can be controlled placing a doped graphene sheet on the proximity of a metallic grating, adding more versatility to this type of system. We develop a semi-analytical model, based on a perfect-metal diffraction grating. This model allows to reproduce well FDTD calculations for the same problem but with much less computer time. We discuss the optical properties of the system covering a spectral range spanning the interval from the THz to the mid-IR. It is shown that the system can be used as both a perfect absorber and a sensing device. For illustrating the latter property we have chosen different alcohols as analytes. The frequency at which perfect absorption appears can be controlled by the geometric parameters of the grating and by the value of the Fermi energy in graphene. The theoretical results predicted throughout this work can be verified experimentally in the future.

cond-mat.mes-hall↗