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Christian Nicolaisen Hansen

Publications and source records attributed to Christian Nicolaisen Hansen.

3 recordsLinked to original sources

Theoretical investigation of two-dimensional semiconductor nanoribbons and nanoparticles for tailored light--matter interactions

We explore theoretically the optical response of two-dimensional (2D) materials patterned at the nanoscale into either arrays of ribbons along a planar surface or spherical particles. Fourier-Floquet decomposition of the electromagnetic fields is used in order to obtain the reflectance, transmittance and absorbance of the nanoribbon array. The spherical particles are treated with Mie theory, with the boundary conditions modified to accommodate a surface conductivity at the interface. We consider the excitonic response of hexagonal boron nitride in the ultraviolet, and of the transition-metal dichalcogenide WS2 in the visible. Unlike what is expected from graphene, where plasmons have proven very sensitive to geometry, the excitonic response of nanoribbon arrays is found to show weak tunability with the array parameters. To enhance tunability with the geometry of the system, or via hybridization with the substrate, nanospheres with a 2D semiconductor coating are demonstrated to provide a superior platform. Overall, we find that the localized nature of excitons in 2D semiconductors largely limits tunability with geometry, but their hybridization with other optical modes in the nanopatterning setup still holds promise for controllable light--matter interactions.

cond-mat.mes-hall↗

Velocity-tunable exciton-photon hybridization in cathodoluminescence

Exciton-photon hybridization is typically realised in geometrically defined optical cavities, where tunability is achieved by modifying either the cavity or the excitonic medium. Here we investigate transition-radiation interferences in suspended subwavelength films resembling a free-electron-defined resonance and explore their interaction with excitons in transition metal dichalcogenides. We demonstrate that these resonances hybridize with excitonic transitions and can be tuned continuously by varying the electron energy. The resulting detuning depends on both film thickness and electron velocity, establishing the latter as an external and continuous knob for exciton-photon coupling. This approach enables tunable hybridization without structural modification and provides a free-electron-driven nanoscale platform for studying exciton-light interactions.

physics.optics↗

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↗