arXiv subjects

Bernhard Urbaszek

Publications and source records attributed to Bernhard Urbaszek.

At least 19 recordsLinked to original sources

arXiv2026

Spatially-resolved multiphoton photoemission from a lateral transition metal dichalcogenide heterostructure

Transition metal dichalcogenides (TMDs) in their monolayer form offer a premier platform for next-generation optoelectronics, particularly through the local manipulation of their robust excitonic states using nanoscale electric fields. These localized states can be dynamically controlled through spatial structuring as well as through ultrafast field modulations driven by tailored optical pulses. Characterizing the resulting rapid, nanoscale charge carrier dynamics requires a technique with exceptional spatial and temporal resolution. Here, we report on the spatio-temporally resolved investigation of ground state and excited state photoemission from a lateral heterostructure built of monolayers of WSe$_2$ and MoSe$_2$ using few-cycle light pulses with a photon energy of 0.62 eV. We utilize photoemission electron microscopy to spatially resolve the highly nonlinear photoemission from the monolayer structure with few tens of nanometer resolution. By varying the laser pulse energy, we extract the nonlinearity of the photoemission process and thus the dynamic binding energy of the photoelectrons before and after optical excitation with high spatial and temporal resolution.

physics.optics↗

arXiv2026

Probing Nonlinear Interactions of Dipolar Interlayer Excitons in MoSe$_2$/WSe$_2$ Heterobilayers

Interlayer excitons in transition-metal dichalcogenide heterobilayers possess intrinsic out-of-plane dipole moments, providing a platform for investigating exciton-exciton interactions at high densities. Here, we use excitation-energy-dependent photoluminescence excitation (PLE) spectroscopy to probe the nonlinear response of dipolar interlayer excitons in chemical vapor deposition-grown MoSe$_2$/WSe$_2$ heterobilayers. By tuning the excitation energy across intralayer exciton resonances at fixed excitation power, we selectively vary the population injected into the interlayer exciton states. Resonant excitation drives the system into a nonlinear regime, leading to saturation of the interlayer exciton photoluminescence and an apparent broadening of the intralayer $1s$ resonances in the PLE spectra. At the same time, the interlayer exciton emission exhibits a pronounced blueshift, reaching approximately 2.5 meV at 4 K and 1 meV at 75 K. The blueshift increases systematically with the interlayer exciton population and is consistent with a net repulsive exciton-exciton interaction, with contributions from dipole-dipole repulsion in the density regime investigated. Our results establish PLE as a sensitive approach for accessing the nonlinear, high-density regime of interlayer excitons and probing their interactions in van der Waals heterostructures.

cond-mat.mes-hall↗

arXiv2026

Excitonic fingerprints of magnetic configurations and switching in multilayer CrSBr

The coupling between electronic states and magnetism provides a route towards optical readout and control of magnetic information. In the magnetic semiconductor CrSBr, excitons are coupled to magnetic order, making their optical response sensitive to the underlying magnetization. Here, we show that the energy and oscillator strength of bulk and surface excitons provide distinct spectroscopic fingerprints of magnetic configurations and switching pathways. We distinguish domain-wall-mediated magnetization reversal, manifested by continuous spectral evolution as a domain wall traverses the optical spot, from abrupt, large-area magnetization reversal. Using the resulting excitonic fingerprints, we reconstruct successive magnetic configurations in 4- and 5-layer CrSBr during the transition from ferromagnetic to antiferromagnetic order. We further find that the sensitivity to magnetic order is strongly exciton-dependent: low-energy excitons resolve intermediate and surface-related configurations, whereas a higher-energy exciton predominantly exhibits a transfer of oscillator strength between ferromagnetic and antiferromagnetic resonances. These results establish excitonic spectroscopy as a sensitive probe of layer-dependent magnetic configurations and their switching pathways in layered magnetic semiconductors.

cond-mat.mtrl-sci↗

arXiv2026

Detecting Magnetic Phase Transitions in Ion-Irradiated CrSBr Through Resonant Raman Scattering

Controlling magnetic phases and accurately determining their transition temperatures are essential for the development of low-dimensional magnetic materials. Here, we demonstrate that He$^+$ ion irradiation provides a versatile route for engineering magnetic phases in layered CrSBr and establish temperature-dependent polarization-resolved Raman spectroscopy as a sensitive optical probe for identifying irradiation-induced magnetic phase transitions. We reveal that the magnetic response of the modified CrSBr is governed by both irradiation dose and crystal thickness. The temperature evolution of the Raman tensor elements resolves the antiferromagnetic transition in pristine CrSBr at T$_N \approx 132$ K as well as irradiation-induced magnetic transitions at T$_C \approx 105-110$ K and T$_D \approx 40$ K corresponding to ferromagnetic and defect-related magnetic phase transitions. Complementary magneto-optical measurements confirm the progressive suppression of antiferromagnetic order and the emergence of new defect-engineered magnetic phases, including pure ferromagnetic behavior at high irradiation doses. These findings establish irradiated CrSBr as a platform for controllable magnetic phase engineering while demonstrating polarization-resolved Raman spectroscopy as a rapid, non-destructive, and broadly applicable method for probing magnetic phase transitions in van der Waals magnets.

cond-mat.mtrl-sci↗

arXiv2026

Role of a Quarter-Wave Plate in Confocal Microscopy: Signature of Spin-Orbit Interactions

Spin-orbit interactions of light couple polarization and spatial degrees of freedom, underpinning phenomena such as the spin Hall effect of light. Although widely explored at interfaces and in tightly focused beams, their impact in nominally paraxial confocal systems remains largely unexamined. Here we show that a single quarter-wave plate embedded in a simple confocal geometry between polarizers can strongly reshape the transverse structure of a Gaussian beam. We observe an enhancement of the polarization extinction ratio by more than two orders of magnitude, accompanied by a transformation of the Gaussian intensity profile into a first-order Hermite-Gaussian-like two-lobe mode. The orientation of this pattern is continuously tunable via rotation of the wave plate, evidencing polarization-controlled reorientation of the transverse field. To explain these observations, we introduce a minimal extension of Jones matrix formalism incorporating complex parameters that quantitatively reproduces the measurements. Our results uncover a previously overlooked form of spin-orbit-mediated mode control in standard confocal optics and establish a simple route to on-demand spatial mode engineering for applications in resonant spectroscopy, optical imaging and quantum optics.

physics.optics↗

arXiv2026

CVD Grown Hybrid MoSe$_2$-WSe$_2$ Lateral/Vertical Heterostructures with Strong Interlayer Exciton Emission

Lateral heterostructures of 2D transition metal dichalcogenide offer a powerful platform to investigate photonic and electronic phenomena at atomically sharp interfaces. However, their controlled engineering, including tuning lateral domain size and integration into vertical van der Waals heterostructures with other 2D materials, remains challenging. Here, we present a facile route for the synthesis of two types of heterostructures consisting of monolayers of MoSe$_2$ and WSe$_2$ - purely lateral (HS I) and hybrid lateral/vertical (HS II) - using liquid precursors of transition metal salts and chemical vapor deposition (CVD). Depending on the growth parameters, the heterostructure type and their lateral dimensions can be adjusted. We characterized properties of the HS I and HS II by complementary spectroscopic and microscopic techniques including Raman and photoluminescence spectroscopy, and optical and atomic force microscopy, and scanning electron and transmission electron microscopy. The photoluminescence measurements reveal strong interlayer exciton emission in the MoSe$_2$/WSe$_2$ region of HS II, which dominates the spectrum at 4 K and persisting up to room temperature. These results demonstrate high optical quality of the grown heterostructures which in combination with scalability of the developed approach paves the way for fundamental studies and device applications based on these unique 2D quantum materials.

cond-mat.mtrl-sci↗

arXiv2025

Twist-tuned exchange and hysteresis in a bilayer van der Waals magnet

Moir\'e superlattices in twisted bilayers enable profound reconstructions of the electronic bandstructure, giving rise to correlated states with remarkable tunability. Extending this paradigm to van der Waals magnets, twisting creates spatially varying interlayer exchange interactions that stabilize emergent spin textures and the coexistence of ferromagnetic and antiferromagnetic domains. Here, we demonstrate the emergence of robust magnetic hysteresis in bilayer CrSBr upon twisting by an angle of ~ 3{\deg}. This is observed as the corresponding hysteretic evolution of the exciton energy, that directly correlates with the bilayer magnetic state, in magnetic field dependent photoluminescence measurements. A two-sublattice model captures this behavior, attributing it to the twist-induced reduction of interlayer exchange that stabilizes both parallel and antiparallel spin configurations across a broad field range. Comparison with experiment enables quantitative extraction of the effective exchange strength. Remarkably, the system exhibits coherent averaging across the moir\'e supercell, yielding an effective monodomain response characterized by switching into the antiferromagnetic state, rather than forming spin textures or fragmented domains. Spatially resolved measurements further uncover local variations in hysteresis loops, consistent with position-dependent modulation of the average exchange interaction. Our results establish twist engineering as a powerful route to programmable magnetic memories in two-dimensional magnets, harnessing the robustness of antiferromagnetic order.

cond-mat.mtrl-sci↗

arXiv2025

Interplay of vibrational, electronic, and magnetic states in CrSBr

The van der Waals antiferromagnet CrSBr exhibits coupling of vibrational, electronic, and magnetic degrees of freedom, giving rise to distinctive quasi-particle interactions. We investigate these interactions across a wide temperature range using polarization-resolved Raman spectroscopy at various excitation energies, complemented by optical absorption and photoluminescence excitation (PLE) spectroscopy. Under 1.96 eV excitation, we observe pronounced changes in the A$_g^1$, A$_g^2$, and A$_g^3$ Raman modes near the N\'eel temperature, coinciding with modifications in the oscillator strength of excitonic transitions and clear resonances in PLE. The distinct temperature evolution of Raman tensor elements and polarization anisotropy for Raman modes indicates that they couple to different excitonic and electronic states. The suppression of the excitonic state's oscillation strength above the N\'eel temperature could be related to the magnetic phase transition, thereby connecting these excitonic states and Raman modes to a specific spin alignment. These observations make CrSBr a versatile platform for probing quasi-particle interactions in low-dimensional magnets and provide insights for applications in quantum sensing and quantum communication.

cond-mat.mtrl-sci↗

arXiv2025

Silicon nanoantennas for tailoring the optical properties of MoS2 monolayers

Silicon-based dielectric nanoantennas provide an effective platform for engineering light-matter interactions in van der Waals semiconductors. Here, we demonstrate near-field coupling between monolayer MoS2 and silicon nanoantennas arranged in hexagonal lattices with tunable geometric parameters, leading to a three-fold enhancement in photoluminescence and an excitation-wavelength-dependent emission that aligns with Mie-resonant modes. Raman spectroscopy reveals an up to 8-fold enhancement in the vibrational modes of MoS2, while second-harmonic generation exhibits a 20 to 30-fold increase in efficiency, closely correlating with the presence of the underlying nanoantennas. Our experiments and simulations quantify the tunable benefits of the near-field interactions, taking into account thin-film interference and strain-induced effects. Our findings present dielectric nanoantennas as a promising platform for tailoring linear and nonlinear optical properties in 2D materials, with potential applications in nanophotonic devices and integrated photonics.

physics.optics↗

arXiv2025

Magnetic Correlation Spectroscopy in CrSBr

CrSBr is an air-stable magnetic van der Waals semiconductor with strong magnetic anisotropy, where the interaction of excitons with the magnetic order enables the optical identification of different magnetic phases. Here, we study the magnetic anisotropy of multi-layer CrSBr inside a three-axis vector magnet and correlate magnetic order and optical transitions in emission and absorption. We identify layer by layer switching of the magnetization through drastic changes of the optical emission and absorption energy and strength as a function of the applied magnetic field. We correlate optical transitions in reflection spectra with photoluminescence (PL) emission using a transfer-matrix analysis and find that ferromagnetic and antiferromagnetic order between layers can coexist in the same crystal. In the multi-peak PL emission the intensity of energetically lower lying transitions reduces monotonously with increasing field strength whereas energetically higher lying transitions around the bright exciton $X_B$ brighten close to the saturation field. Using this contrasting behavior we can therefore correlate transitions with each other.

cond-mat.mtrl-sci↗

arXiv2025

Impact of charge transfer excitons on unidirectional exciton transport in lateral TMD heterostructures

Lateral heterostructures built of monolayers of transition metal dichalcogenides (TMDs) are characterized by a thin 1D interface exhibiting a large energy offset. Recently, the formation of spatially separated charge-transfer (CT) excitons at the interface has been demonstrated. The technologically important exciton propagation across the interface and the impact of CT excitons has remained in the dark so far. In this work, we microscopically investigate the spatiotemporal exciton dynamics in the exemplary hBN-encapsulated WSe$_2$-MoSe$_2$ lateral heterostructure and reveal a highly interesting interplay of energy offset-driven unidirectional exciton drift across the interface and efficient capture into energetically lower CT excitons at the interface. This interplay triggers a counterintuitive thermal control of exciton transport with a less efficient propagation at lower temperatures - opposite to the behavior in conventional semiconductors. We predict clear signatures of this intriguing exciton propagation both in far- and near-field photoluminescence experiments. Our results present an important step toward a microscopic understanding of the technologically relevant unidirectional exciton transport in lateral heterostructures.

cond-mat.mes-hall↗

arXiv2024

Raman Polarization Switching in CrSBr

Semiconducting CrSBr is a layered A-type antiferromagnet, with individual layers antiferromagnetically coupled along the stacking direction. Due to its unique orthorhombic crystal structure, CrSBr exhibits highly anisotropic mechanical and optoelectronic properties acting itself as a quasi-1D material. CrSBr demonstrates complex coupling phenomena involving phonons, excitons, magnons, and polaritons. Here we show through polarization-resolved resonant Raman scattering the intricate interaction between the vibrational and electronic properties of CrSBr. For samples spanning from few-layer to bulk thickness, we observe that the polarization of the A$_g^2$ Raman mode can be rotated by 90 degrees, shifting from alignment with the crystallographic a (intermediate magnetic) axis to the b (easy magnetic) axis, depending on the excitation energy. In contrast, the A$_g^1$ and A$_g^3$ modes consistently remain polarized along the b axis, regardless of the laser energy used. We access real and imaginary parts of the Raman tensor in our analysis, uncovering resonant electron-phonon coupling.

cond-mat.mtrl-sci↗

arXiv2024

Two dimensional semiconductors: optical and electronic properties

In the last decade atomically thin 2D materials have emerged as a perfect platform for studying and tuning light-matter interaction and electronic properties in nanostructures. The optoelectronic properties in layered materials such as transition-metal-dichalcogenides (TMDs) are governed by excitons, Coulomb bound electron-hole pairs, even at room temperature. The energy, wave function extension, spin and valley properties of optically excited conduction electrons and valence holes are controllable via multiple experimentally accessible knobs, such as lattice strain, varying atomic registries, dielectric engineering as well as electric and magnetic fields. This results in a multitude of fascinating physical phenomena in optics and transport linked to excitons with very specific properties, such as bright and dark excitons, interlayer and charge transfer excitons as well as hybrid and moir\'e excitons. In this book chapter we introduce general optoelectronic properties of 2D materials and energy landscapes in TMD monolayers as well as their vertical and lateral heterostructures, including twisted TMD hetero- and homobilayer bilayers with moir\'e excitons and lattice recombination effects. We review the recently gained insights and open questions on exciton diffusion, strain- and field-induced exciton drift. We discuss intriguing non-linear many-particle effects, such as exciton halo formation, negative and anomalous diffusion, the surprising anti-funneling of dark excitons.

cond-mat.mes-hall↗

arXiv2023

Kapitza-resistance-like exciton dynamics in atomically flat MoSe$_{2}$-WSe$_{2}$ lateral heterojunction

Being able to control the neutral excitonic flux is a mandatory step for the development of future room-temperature two-dimensional excitonic devices. Semiconducting Monolayer Transition Metal Dichalcogenides (TMD-ML) with extremely robust and mobile excitons are highly attractive in this regard. However, generating an efficient and controlled exciton transport over long distances is a very challenging task. Here we demonstrate that an atomically sharp TMD-ML lateral heterostructure (MoSe$_{2}$-WSe$_{2}$) transforms the isotropic exciton diffusion into a unidirectional excitonic flow through the junction. Using tip-enhanced photoluminescence spectroscopy (TEPL) and a modified exciton transfer model, we show a discontinuity of the exciton density distribution on each side of the interface. We introduce the concept of exciton Kapitza resistance, by analogy with the interfacial thermal resistance referred to as Kapitza resistance. By comparing different heterostructures with or without top hexagonal boron nitride (hBN) layer, we deduce that the transport properties can be controlled, over distances far greater than the junction width, by the exciton density through near-field engineering and/or laser power density. This work provides a new approach for controlling the neutral exciton flow, which is key toward the conception of excitonic devices.

cond-mat.mes-hall↗

arXiv2023

Interface engineering of charge-transfer excitons in 2D lateral heterostructures

The existence of bound charge transfer (CT) excitons at the interface of monolayer lateral heterojunctions has been debated in literature, but contrary to the case of interlayer excitons in vertical heterostructure their observation still has to be confirmed. Here, we present a microscopic study investigating signatures of bound CT excitons in photoluminescence spectra at the interface of hBN-encapsulated lateral MoSe$_2$-WSe$_2$ heterostructures. Based on a fully microscopic and material-specific theory, we reveal the many-particle processes behind the formation of CT excitons and how they can be tuned via interface- and dielectric engineering. For junction widths smaller than the Coulomb-induced Bohr radius we predict the appearance of a low-energy CT exciton. The theoretical prediction is compared with experimental low-temperature photoluminescence measurements showing emission in the bound CT excitons energy range. Our joint theory-experiment study presents a significant step towards a microscopic understanding of optical properties of technologically promising 2D lateral heterostructures.

cond-mat.mes-hall↗

arXiv2023

Highly Tunable Ground and Excited State Excitonic Dipoles in Multilayer 2H-MoSe$_2$

The fundamental properties of an exciton are determined by the spin, valley, energy, and spatial wavefunctions of the Coulomb bound electron and hole. In van der Waals materials, these attributes can be widely engineered through layer stacking configuration to create highly tunable interlayer excitons with static out-of-plane electric dipoles, at the expense of the strength of the oscillating in-plane dipole responsible for light-matter coupling. Here we show that interlayer excitons in bi- and tri-layer 2H-MoSe$_2$ crystals exhibit electric-field-driven coupling with the ground ($1s$) and excited states ($2s$) of the intralayer A excitons. We demonstrate that the hybrid states of these distinct exciton species provide strong oscillator strength, large permanent dipoles (up to $0.73 \pm 0.01$ enm), high energy tunability (up to $\sim$ 200 meV), and full control of the spin and valley characteristics such that the exciton g-factor can be manipulated over a large range (from -4 to +14). Further, we observe the bi- and tri-layer excited state ($2s$) interlayer excitons and their coupling with the intralayer excitons states ($1s$ and $2s$). Our results, in good agreement with a coupled oscillator model with spin (layer)-selectivity and beyond standard density functional theory calculations, promote multilayer 2H-MoSe$_2$ as a highly tunable platform to explore exciton-exciton interactions with strong light-matter interactions.

cond-mat.mes-hall↗

arXiv2022

Probing the optical near-field interaction of Mie nanoresonators with atomically thin semiconductors

Optical Mie resonators based on silicon nanostructures allow tuning of light-matter-interaction with advanced design concepts based on CMOS compatible nanofabrication. Optically active materials such as transition-metal dichalcogenide (TMD) monolayers can be placed in the near-field region of such Mie resonators. Here, we experimentally demonstrate and verify by numerical simulations coupling between a MoSe2 monolayer and the near-field of dielectric nanoresonators. Through a comparison of dark-field (DF) scattering spectroscopy and photoluminescence excitation experiments (PLE), we show that the MoSe2 absorption can be enhanced via the near-field of a nanoresonator. We demonstrate spectral tuning of the absorption via the geometry of individual Mie resonators. We show that we indeed access the optical near-field of the nanoresonators, by measuring a spectral shift between the typical near-field resonances in PLE compared to the far-field resonances in DF scattering. Our results prove that using MoSe2 as an active probe allows accessing the optical near-field above photonic nanostructures, without the requirement of highly complex near-field microscopy equipment.

physics.optics↗

arXiv2022

Inverse design with flexible design targets via deep learning: Tailoring of electric and magnetic multipole scattering from nano-spheres

Deep learning is a promising, ultra-fast approach for inverse design in nano-optics, but despite fast advancement of the field, the computational cost of dataset generation, as well as of the training procedure itself remains a major bottleneck. This is particularly inconvenient because new data need to be generated and a new network needs to be trained for any modification of the problem. We propose a technique that allows to train a single neural network on a broad range of design targets without any re-training. The key idea of our method is to enrich existing data with random "regions of interest" (ROI) labels. A model trained on such ROI-decorated data becomes capable to operate on a broad range of physical targets, while it learns to focus its design effort on a user-defined ROI, ignoring the rest of the physical domain. We demonstrate the method by training a tandem-network on the design of dielectric core-shell nano-spheres for electric and magnetic dipole and quadrupole scattering over a broad spectral range. The network learns to tailor very distinct, flexible design targets like scattering due to specific multipoles in narrow spectral windows. Varying the design problem does not require any re-training. Our approach is very general and can be directly used with existing datasets. It can be straightforwardly applied to other network architectures and problems.

physics.optics↗