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Jakub Regner

Publications and source records attributed to Jakub Regner.

5 recordsLinked to original sources

Stabilizing van der Waals NbOI2 by SiO2 encapsulation for Photonic Applications

Niobium oxide diiodide (NbOI2) is an emerging material for photonics and electronics, distinguished by its exceptional second-order nonlinearity and pronounced in-plane ferroelectricity, both originating from its highly anisotropic ABC-stacked crystal structure. Its broken inversion symmetry enables its optical nonlinear efficiency to scale with thickness, making multilayer NbOI2 highly promising for nonlinear frequency conversion like second harmonic generation or and spontaneous parametric down-conversion in bulk or waveguides. However, under ambient conditions NbOI2 degrades into an amorphous oxide within weeks, severely diminishing its nonlinear response. To overcome this, we investigate SiO2 encapsulation via physical vapor deposition to protect NbOI2 multilayers from environmental degradation. Our systematic study reveals that encapsulation preserves structural integrity and nonlinear optical performance, establishing NbOI2 as a stable candidate for heterogeneous integration in foundry-compatible photonic platforms and quantum technologies.

physics.optics

Tunable magnetism in 2D organic-ion-intercalated MnPS3 via molecule-dependent vacancy generation

The magnetic properties of van der Waals materials are profoundly influenced by structural defects. The layered antiferromagnet MnPS3 offers a unique opportunity to explore defect-related magnetism, as Mn2+ vacancies can be generated by the intercalation of specific guest molecules. However, the effectiveness of this process in atomically thin flakes and the extent of the magnetic tunability remain unclear. Here, we show that the magnetic properties of MnPS3 can be tailored through the intercalation of different guest molecules. Notably, the insertion of four alkylammonium ions introduces different populations of Mn2+ vacancies, leading to a transition from the pristine antiferromagnetic state to more complex magnetic textures, including a ferrimagnetic state displaying a magnetic saturation of 1 uB/atom. Moreover, we show that the intercalation of few-nm-thick flakes also leads to the emergence of a ferrimagnetic response. This in-flake intercalation, which can be monitored in real time using optical microscopy, can be interrupted before completion, generating lateral heterostructures between pristine and intercalated areas. This approach opens the way to the use of partial intercalation to define regions with distinct magnetic properties within a single flake.

cond-mat.mtrl-sci

Exciton-polariton condensate in the van der Waals magnet CrSBr

Van der Waals magnets are an emergent material class of paramount interest for fundamental studies in coupling light with matter excitations, which are uniquely linked to their underlying magnetic properties. Among these materials, the semiconducting magnet CrSBr is possibly a first playground where we can study simultaneously the interaction of photons, magnons, and excitons at the quantum level. Here we demonstrate a coherent macroscopic quantum phase, the bosonic condensation of exciton-polaritons, emerging in a CrSBr flake embedded in a fully tunable cryogenic open optical cavity. The Bose condensate is characterized by a highly non-linear threshold-like behavior, and coherence manifests distinctly via its first and second order quantum correlations. We find that the condensate's non-linearity is highly susceptible to the magnetic order in CrSBr. Specially, it can encounter a sign change from attractive to repulsive interactions when the intrinsic antiferromagnetic order transforms to the forced ferromagnetic order. Our findings open a route towards magnetically controllable quantum fluids of light, and optomagnonic devices where spin magnetism is coupled to on-chip Bose-Einstein condensates.

cond-mat.mtrl-sci

Resonant X-ray spectroscopies on Chromium $3\textit{d}$ orbitals in CrSBr

We investigate the Cr electronic structure and excitations in CrSBr, a layered magnetic semiconductor, using a combination of resonant x-ray spectroscopic techniques. X-ray absorption spectroscopy (XAS) and resonant inelastic x-ray scattering (RIXS) spectra collected at the Cr $L_{2,3}$ edges reveal significant linear dichroism, which arises from the distorted octahedral environment surrounding the Cr$^{3+}$ ions. The origin of the bright excitons observed in this compound is examined through a comparison of the d-d excitations identified in the RIXS spectra, the x-ray excited optical luminescence (XEOL) spectra, and previously reported optical spectroscopic and theoretical studies. To further understand these phenomena, we develop a multiplet model based on a crystal electric field (CEF) approach that accounts for the local environment of Cr ions. This model successfully reproduces several experimental features, while also suggesting strong hybridization effects between Cr $3\textit{d}$ orbitals and ligands that are not fully captured by the present framework. These findings advance our understanding of the electronic structure and excitonic behavior in CrSBr and provide a foundation for future $\textit{in-situ}$ and $\textit{operando}$ studies of CrSBr-based devices for spintronic and optoelectronic applications.

cond-mat.mtrl-sci

Enhanced Magnetization by Defect-Assisted Exciton Recombination in Atomically Thin CrCl$_3$

Two dimensional (2D) semiconductors present unique opportunities to intertwine optical and magnetic functionalities and to tune these performances through defects and dopants. Here, we integrate exciton pumping into a quantum sensing protocol on nitrogen-vacancy centers in diamond to image the optically-induced transient stray fields in few-layer, antiferromagnetic CrCl$_3$. We discover that exciton recombination enhances the in-plane magnetization of the CrCl$_3$ layers, with a predominant effect in the surface monolayers. Concomitantly, time-resolved photoluminescence measurements reveal that nonradiative exciton recombination intensifies in atomically thin CrCl$_3$ with tightly localized, nearly dipole-forbidden excitons and amplified surface-to-volume ratio. Supported by experiments under controlled surface exposure and density functional theory calculations, we interpret the magnetically enhanced state to result from a defect-assisted Auger recombination that optically activates electron transfer between water vapor related surface impurities and the spin-polarized conduction band. Our work validates defect engineering as a route to enhance intrinsic magnetism in single magnetic layers and opens a novel experimental platform for studying optically-induced, transient magnetism in condensed matter systems.

cond-mat.mtrl-sci