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Fabian Felixberger

Publications and source records attributed to Fabian Felixberger.

2 recordsLinked to original sources

Near-Field Characterisation of Guided Modes in WS2 Nanobeams and Quasi-Bulk Crystals

The exceptionally high in-plane refractive index, low sub-bandgap absorption, and strong optical anisotropy of WS2 make it a promising material platform for next-generation integrated circuits for nanophotonics. Its layered van der Waals structure further enables heterogeneous integration with silicon photonics and emerging two-dimensional optoelectronic materials. However, despite increasing interest in the waveguiding properties of WS2, experimental studies of wavelength-dependent modal confinement and attenuation remain limited. Additionally, though the extinction coefficient of WS2 is expected to be near-negligible beneath the bandgap, reported values span orders of magnitude, leading to large uncertainty in predicted modal decay lengths and wafer-scale integration feasibility. To resolve these ambiguities we perform hyperspectral cavity-enhanced imaging, determining high-resolution upper and lower bounds on the extinction coefficient of WS2 within the visible-NIR edge. We further employ scattering-type scanning near-field optical microscopy (s-SNOM) to probe TE0, TM0, and higher-order modes in both quasi-bulk and nanobeam WS2 waveguides across the 800-1400 nm spectral range, enabling identification of mode-specific trends in wavevector dispersion and loss. This work simultaneously assesses s-SNOM as a probe of waveguide performance, and we find that while absolute loss values depend on measurement geometry, s-SNOM reliably captures relative modal trends and provides upper bounds on propagation loss, supporting its use as a diagnostic tool for anisotropic waveguides. We further identify significant artefacts in nanobeam measurements arising from transverse interference and spatial sampling effects when the structure size approaches the excitation wavelength, which can shift extracted effective indices by up to 0.25.

physics.optics

Charge Transfer from Perovskite Quantum Dots to Multifunctional Ligands with Tethered Molecular Species

Perovskite quantum dots (pQDs) are promising materials for optoelectronic and photocatalytic applications due to their unique optical properties. To enhance charge carrier extraction or injection donor/acceptor molecules can be tethered to the pQD. These molecules must strongly bind to the ionic surfaces of pQDs without compromising colloidal stability. These we achieve by using multifunctional ligands containing a quaternary ammonium binding group for strong pQDs surface attachment, a long tail group for colloidal stability, and a functional group near the pQD surface. Such pQDs with ferrocene-functionalized ligands show fast photoexcited hole transfer with near-unity efficiency. Density functional theory calculations reveal how ferrocene's molecular structure reorganizes following hole transfer, affecting its charge separation efficiency. This approach can also be extended to in photoexcited electron and energy transfer processes with pQDs. Therefore, this strategy offers a blueprint for creating efficient QD-molecular hybrids for applications like photocatalysis.

cond-mat.mtrl-sci