arXiv subjects

P. Elli Stamatopoulou

Publications and source records attributed to P. Elli Stamatopoulou.

9 recordsLinked to original sources

arXiv2026

Surface quantum response of plasmonic heterodimers: revealing the hidden nonlocality

We probe the quantum response of plasmonic heterodimers with extended (plane waves) and localized (point dipoles and electron beams) sources. Implementing the surface-response formalism based on Feibelman parameters, we explore nanosphere heterodimers where one particle is characterized by electron spill-in, while the other by spill-out. We identify situations where the two quantum surface corrections that act in opposite spectral-shift directions can cancel out, producing mesoscopic spectra that do not differ from the predictions of the local-response approximation. This picture changes dramatically once localized sources are implemented, allowing one to selectively probe the quantum response of the particles independently. Such probing occurs in terms of higher-order modes in the case of electron beams, or for the complete modal landscape in the case of point dipole sources. This description offers a new insight into the mechanisms governing light--matter interactions in extreme plasmonic architectures, and opens new perspectives for the understanding and tailoring of plasmonic--quantum emitter architectures.

physics.optics↗

arXiv2026

T-matrix scattering formalism for electron-beam spectroscopy

Advanced computational tools that describe the interaction of electrons with structured nanophotonic devices are crucial for theoretical predictions, specific design tasks, and the interpretation of experimental results. These tools open the door to a systematic exploration of light-matter interactions in complex photonic environments and support the development of next-generation nanophotonic platforms. Here, we report on the implementation of electron-beam spectroscopy in a T-matrix-based scattering formulation. Such a framework is quite versatile in predicting the electromagnetic response of complex photonic materials composed of periodically or aperiodically arranged individual scatterers. By extending this formalism to describe interactions with fast electrons, we provide a fast and accurate numerical tool for simulating cathodoluminescence (CL) and electron energy-loss spectroscopy (EELS) measurements. The desired functionalities are implemented in treams_ebeam, an extension of the existing software suite treams for electromagnetic scattering computations, available at https://github.com/tfp-photonics/treams_ebeam. We demonstrate the implementation details on a carefully selected set of problems, including single scatterers of various shapes and materials, a periodic chain of elliptical nanodisks, and a finite cluster of nanospheres arranged in a two-dimensional (2D) lattice. By uniting fast-electron physics with advanced scattering theory, our framework unlocks new possibilities for designing, understanding, and engineering next-generation nanoscale light-matter interactions.

physics.comp-ph↗

arXiv2026

Probing strong coupling in core--shell nanoparticles with fast electron beams

Collective optical excitations, such as localized surface plasmons in metallic nanoparticles and Mie resonances in high-index dielectrics, play a central role in nanoscale light--matter interactions. When such optical modes interact with electronic transitions in matter under suitable conditions, they can couple strongly, analogous to two coupled harmonic oscillators, forming hybrid light--matter states. In this work, we probe this coupling in core--shell nanoparticles using fast electrons in electron energy-loss (EEL) and cathodoluminescence (CL) spectroscopy. Owing to their highly localized fields, fast electrons can excite modes inaccessible with light-based spectroscopies, including higher-order nonradiative modes, which offer greater field confinement and potentially stronger coupling. Here, we develop an analytical framework to calculate the EEL and CL probabilities for spherical core--shell nanoparticles under aloof and penetrating electron trajectories. This formalism is applied to two representative systems: an excitonic core with a metallic shell, and a silicon core with an excitonic shell. Our main focus is to examine how the electron beam position and velocity affect our ability to probe this coupling. Depending on the electron beam parameters, we find that the spectral signature of strong coupling remains robust in plasmonic nanospheres. In contrast, it can be significantly suppressed or even completely obscured in dielectric nanospheres. Our developed formalism enables a deeper understanding of the coupling mechanisms in electron--light--matter interactions, thereby accelerating progress in single-nanoparticle-based polaritonic studies.

physics.optics↗

arXiv2024

Electron beams traversing spherical nanoparticles: analytic and numerical treatment

We present an analytic, Mie theory-based solution for the energy-loss and the photon-emission probabilities in the interaction of spherical nanoparticles with electrons passing nearby and through them, in both cathodoluminescence and electron energy-loss spectroscopies. In particular, we focus on the case of penetrating electron trajectories, for which the complete fully electrodynamic and relativistic formalism has not been reported as yet. We exhibit the efficiency of this method in describing collective excitations in matter through calculations for a dispersive and lossy system, namely a sphere described by a Drude permittivity. Subsequently, we use the analytic solution to corroborate the implementation of electron-beam sources in a state-of-the-art numerical method for problems in electrodynamics, the discontinuous Galerkin time-domain (DGTD) method. We show that the two approaches produce spectra in good mutual agreement, and demonstrate the versatility of DGTD via simulations of spherical nanoparticles characterized by surface roughness. The possibility of simultaneously employing both kinds of calculations (analytic and numerical) facilitates a better understanding of the rich optical response of nanophotonic architectures excited by fast electron beams.

cond-mat.mes-hall↗

arXiv2023

Quantum-informed plasmonics for strong coupling: the role of electron spill-out

The effect of nonlocality on the optical response of metals lies at the forefront of research in nanoscale physics and, in particular, quantum plasmonics. In alkali metals, nonlocality manifests predominantly as electron density spill-out at the metal boundary, and as surface-enabled Landau damping. For an accurate description of plasmonic modes, these effects need be taken into account in the theoretical modelling of the material. The resulting modal frequency shifts and broadening become particularly relevant when dealing with the strong interaction between plasmons and excitons, where hybrid modes emerge and the way they are affected can reflect modifications of the coupling strength. Both nonlocal phenomena can be incorporated in the classical local theory by applying a surface-response formalism embodied by the Feibelman parameters. Here, we implement surface-response corrections in Mie theory to study the optical response of spherical plasmonic--excitonic composites in core--shell configurations. We investigate sodium, a jellium metal dominated by spill-out, for which it has been anticipated that nonlocal corrections should lead to an observable change in the coupling strength, appearing as a modification of the width of the mode splitting. We show that, contrary to expectations, the influence of nonlocality on the anticrossing is minimal, thus validating the accuracy of the local response approximation in strong-coupling photonics.

cond-mat.mes-hall↗

arXiv2023

Self-hybridisation between interband transitions and Mie modes in dielectric nanoparticles

We discuss the possibility of self-hybridisation in high-index dielectric nanoparticles, where Mie modes of electric or magnetic type can couple to the interband transitions of the material, leading to spectral anticrossings. Starting with an idealised system described by moderately high constant permittivity with a narrow Lorentzian, in which self-hybridisation is visible for both plane-wave and electron-beam excitation, we embark on a quest for realistic systems where this effect should be visible. We explore a variety of spherical particles made of traditional semiconductors such as Si, GaAs, and GaP. With the effect hardly discernible, we identify two major causes hindering observation of self-hybridisation: the very broad spectral fingerprints of interband transitions in most candidate materials, and the significant overlap between electric and magnetic Mie modes in nanospheres. We thus depart from the spherical shape, and show that interband--Mie hybridisation is indeed feasible in the example of GaAs cylinders, even with a simple plane-wave source. This so-far unreported kind of polariton has to be considered when interpreting experimental spectra of Mie-resonant nanoparticles and assigning modal characters to specific features. On the other hand, it has the potential to be useful for the characterisation of the optical properties of dielectric materials, through control of the hybridisation strength via nanoparticle size and shape.

cond-mat.mes-hall↗

arXiv2022

Reconfigurable chirality with achiral excitonic materials in the strong-coupling regime

We introduce and theoretically analyze the concept of manipulating optical chirality via strong coupling of the optical modes of chiral nanostructures with excitonic transitions in molecular layers or semiconductors. With chirality being omnipresent in chemistry and biomedicine, and highly desirable for technological applications related to efficient light manipulation, the design of nanophotonic architectures that sense the handedness of molecules or generate the desired light polarization in an externally controllable manner is of major interdisciplinary importance. Here we propose that such capabilities can be provided by the mode splitting resulting from polaritonic hybridization. Starting with an object with well-known chiroptical response -- here, for a proof of concept, a chiral sphere -- we show that strong coupling with a nearby excitonic material generates two distinct frequency regions that retain the object's chirality density and handedness, which manifest most clearly through anticrossings in circular-dichroism or differential-scattering dispersion diagrams. These windows can be controlled by the intrinsic properties of the excitonic layer and the strength of the interaction, enabling thus the post-fabrication manipulation of optical chirality. Our findings are further verified via simulations of the circular dichroism of a realistic chiral architecture, namely a helical assembly of plasmonic nanospheres embedded in a resonant matrix.

physics.optics↗

arXiv2022

Disentangling cathodoluminescence spectra in nanophotonics: particle eigenmodes vs transition radiation

Cathodoluminescence spectroscopy performed in an electron microscope has proven a versatile tool for analysing the near- and far-field optical response of plasmonic and dielectric nanostructures. Nevertheless, the transition radiation produced by electron impact is often disregarded in the interpretation of the spectra recorded from resonant nanoparticles. Here we show, experimentally and theoretically, that transition radiation can by itself generate distinct resonances which, depending on the time of flight of the electron beam inside the particle, can result from constructive or destructive interference in time. Superimposed on the eigenmodes of the investigated structures, these resonances can distort the recorded spectrum and lead to potentially erroneous assignment of modal characters to the spectral features. We develop an intuitive analogy that helps distinguish between the two contributions. As an example, we focus on the case of silicon nanospheres, and show that our analysis facilitates the unambiguous interpretation of experimental measurements on Mie-resonant nanoparticles.

cond-mat.mes-hall↗

arXiv2020

Manipulating the photonic Hall effect with hybrid Mie-exciton resonances

We examine the far-field optical response, under-plane wave excitation in the presence of a static magnetic field, of core-shell nanoparticles involving a gyroelectric component, either as the inner or the outer layer, through analytic calculations based on appropriately extended Mie theory. We focus on absorption and scattering of light by bismuth-substituted yttrium iron garnet (Bi:YIG) nanospheres and nanoshells, combined with excitonic materials such as organic-molecule aggregates or two-dimensional transition-metal dichalcogenides, and discuss the hybrid character of the modes emerging from the coupling of the two constituents. We observe the excitation of strong magneto-optic phenomena and explore, in particular, the response and tunability of a magneto-transverse light current, indicative of the photonic Hall effect. We show how interaction between the Bi:YIG and excitonic layers leads to a pair of narrow bands of highly directional scattering, emerging from the aforementioned hybridization, which can be tuned at will by adjusting the geometrical or optical parameters of the system. Our theoretical study introduces optically anisotropic media as promising templates for strong coupling in nanophotonics, offering a means to combine tunable magnetic and optical properties, with potential implications both in the design of all-dielectric photonic devices but also in novel clinical applications.

cond-mat.mes-hall↗