SearcharxivSearch

arXiv subjects

Xuerong Hu

Publications and source records attributed to Xuerong Hu.

14 recordsLinked to original sources

Twist-Reconfigurable van der Waals Moiré Photonic Crystals

Moiré photonics has emerged as a fascinating concept to design and in situ control of the optical bands. Moiré enabled light localisation arises from the relative twist between periodic layers, rather than from fixed, pre-fabricated cavity features. So far, however, the realisation of practical moiré photonic crystals in the visible range has been elusive, due to challenges in engineering nanoscale structures and twisting them dynamically post fabrication. Here, we realise a mechanically reconfigurable moiré photonic crystal, comprising from two patterned van der Waals crystals (tungsten di sulphide, WS$_2$) slabs separated by an optically active hexagonal boron nitride (hBN) spacer. We reconfigured the same pair of WS$_2$ slabs from a twist angle of 3.8° to 8.4° and reconstructed their three-dimensional dispersion using momentum-resolved reflectivity spectroscopy. Further, by reducing the twist angle between the slabs, we observe a denser manifold of folded and hybridised resonances that coincides with a 30-fold enhancement of emission from embedded colour centres. Our results open exciting opportunities for in-situ dispersion engineering and programmable light matter interactions employing van der Waals nanostructures.

physics.optics

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

Magnetic switching of exciton lifetime in CrSBr

Exciton dynamics in layered magnetic semiconductors provide a sensitive probe of the interplay between spin order and light-matter interaction. Here, we study thin CrSBr layers using time-resolved photoluminescence spectroscopy in an external magnetic field, revealing a step-like reduction in the exciton lifetime from 11 to 7 ps, during the magnetization flip from the antiferromagnetic to the ferromagnetic phase. The reduction of the exciton lifetime in the ferromagnetic phase persists below the Néel temperature, as evidenced by its strong magnetic-field dependence that disappears in the paramagnetic phase. Ab initio calculations reveal a one-dimensional nature of free excitons accompanied by a pronounced change in the oscillator strength across the magnetic phase transition predicting a shorter radiative lifetime of free excitons in the antiferromagnetic phase of CrSBr contradicting the experimental observations. This discrepancy is explained by strong localization of excitons at low tempature. We show both experimentally and theoretically that the observed magnetic switching of the exciton lifetime is attributed to a larger exciton localization volume leading to a larger oscillator strength in the ferromagnetic phase. The results show that disorder-induced localization effects play a key role in exciton dynamics in CrSBr.

cond-mat.mes-hall

Polarization- and time-resolved nonlinear multi-photon spectroscopy for confocal microscopy of semiconductor nanostructures

We present a versatile confocal microscopy setup for optical second harmonic generation (SHG) and multi-photon spectroscopy that enables polarization-resolved studies of semiconductor bulk crystals and low-dimensional structures. The system offers full polarization control in both excitation and detection, spatial scanning with micrometer resolution, and spectrally tunable excitation over a broad energy range from 0.5 to 4.0 eV, using femtosecond and picosecond laser pulses. Samples are mounted in a helium-flow cryostat, allowing temperature control from 4 to 300 K. Magnetic fields up to 0.625 T can be applied in the Voigt geometry via an electromagnet. The nonlinear optical signals are analyzed using a high-resolution spectrometer with a spectral resolution of 60 $μ$eV. We demonstrate the potential of the setup by means of SHG polarization tomography measurements on a Cu$_2$O crystal as well as through a SHG spectral scan of a ZnSe crystal over a wide energy range from 1.4 to 3.1 eV. Polarization-resolved confocal SHG mapping of various twisted mono- and bilayer MoS$_2$ structures is also presented. In addition, time-resolved two-color pump-probe experiments are shown for a Cs$_2$AgBiBr$_6$ crystal, illustrating the potential of the system for investigating coherent exciton and phonon dynamics.

cond-mat.mtrl-sci

Photonics in Flatland: Challenges and Opportunities for Nanophotonics with 2D Semiconductors

Two-dimensional (2D) semiconductors are emerging as a versatile platform for nanophotonics, offering unprecedented tunability in optical properties through exciton resonance engineering, van der Waals heterostructuring, and external field control. These materials enable active optical modulation, single-photon emission, quantum photonics, and valleytronic functionalities, paving the way for next-generation optoelectronic and quantum photonic devices. However, key challenges remain in achieving large-area integration, maintaining excitonic coherence, and optimizing amplitude-phase modulation for efficient light manipulation. Advances in fabrication, strain engineering, and computational modelling will be crucial to overcoming these limitations. This perspective highlights recent progress in 2D semiconductor-based nanophotonics, emphasizing opportunities for scalable integration into photonics.

physics.optics

Exciton-polaritons in a monolayer semiconductor coupled to van der Waals dielectric nanoantennas on a metallic mirror

Polaritons in nanophotonic structures have attracted long-standing interest owing to their fundamental importance and potential for applications in nonlinear and quantum optics. Nanoantennas (NAs) made from high refractive index dielectrics offer a suitable platform for polariton physics thanks to the strongly confined optical Mie resonances and low optical losses in contrast to metallic NAs. However, Mie modes are mainly confined within the NA, making inefficient their coupling with excitons in materials deposited externally. Here, we overcome this limitation by using a high-refractive index van der Waals material WS$_2$, which allows straightforward fabrication of NAs on gold. The combination of a 27 nm tall WS$_2$ NA and a gold substrate enables strong modification of the Mie mode distribution and field enhancement inside and in the vicinity of the NA. This allows observation of room-temperature Mie-polaritons (with a Rabi splitting above 80 meV) arising from the strong coupling between Mie modes and the exciton in a monolayer WSe$_2$ placed on WS$_2$/gold NAs. We demonstrate strong nonlinearity of Mie-polaritons, one order of magnitude higher than for excitons in monolayer WSe$_2$ on gold. Our results highlight applicability of van der Waals materials for the realisation of hybrid dielectric-metallic nanophotonics for the study of the strong light-matter interaction.

physics.optics

Topological Jackiw-Rebbi States in Photonic Van der Waals Heterostructures

Topological phenomena, first studied in solid state physics, have seen increased interest for applications in nanophotonics owing to highly controllable light confinement with inherent robustness to defects. Photonic crystals can be designed to host topologically protected interface states for directional light transport, localization and robust lasing via tuning of the bulk topological invariant. At the same time, van der Waals (vdW) materials, in both their monolayer and quasi-bulk forms, are emerging as exciting additions to the field of nanophotonics, with a range of unique optoelectronic properties and intrinsic adherence to any type of host material, allowing fabrication of complex multi-layer structures. We present here a 1D topological photonic platform made from stacked nanostructured and planar layers of quasi-bulk WS$_2$ to achieve Jackiw-Rebbi (JR) interface states between two topologically distinct gratings in the near-infrared range around 750 nm. Such states are measured in the far-field with angle-resolved reflectance contrast measurements, exhibiting linewidth of 10 meV and highly directional emission with an angular bandwidth of 8.0$^\circ$. Subsequent local mapping of the structure via sub-wavelength resolution scattering-type scanning near-field optical microscopy (s-SNOM) reveals strong spatial confinement of the JR state to the grating interface region. Finally, we couple in the JR state the photoluminescence of monolayer WSe$_2$ incorporated in a five-layer vdW grating heterostructure, giving rise to directional enhancement of the excitonic emission of up to 22 times that of uncoupled monolayer, thus demonstrating the potential of the topological interface states for highly directional light emission in addition to light scattering.

physics.optics

Simultaneous observation of bright and dark polariton states in subwavelength gratings made from quasi-bulk WS$_2$

Over the last decade, layered crystals, dubbed van der Waals (vdW) materials, have attracted tremendous interest due to their unique properties in their single and few layer regimes. Their bulk counterparts, however, have only been recently explored as building blocks for nanophotonics as they offer promising properties such as high refractive indices and adherence to any type of substrates. We present here a variety of 1D grating structures composed of bulk transition metal dichalcogenide (TMD) WS$_2$ as a highly tunable and versatile platform for observation of multi-level polaritonic system. The WS$_2$ excitons are simultaneously strongly coupled with the two grating photonic modes including the Bound State in the Continuum (BIC) of the lower energetic mode giving rise to polariton-BICs (pol-BICs). The polaritonic dispersion shapes can be varied in a straightforward fashion by choosing WS$_2$ films of different thicknesses and by changing the period of the grating.

physics.optics

Single photon emitters in monolayer semiconductors coupled to transition metal dichalcogenide nanoantennas on silica and gold substrates

Transition metal dichalcogenide (TMD) single photon emitters (SPEs) offer numerous advantages to quantum information applications, such as high single photon purity and deterministic positioning. Strain in the host monolayer, induced by underlying dielectric Mie resonators, is known to localize their formation to positions co-located with near-field photonic hotspots providing further control over their optical properties. However, traditional materials used for the fabrication of nanoresonators, such as silicon or gallium phosphide (GaP), often require a high refractive index substrate resulting in losses of the emitted light and limited photonic enhancement. Here, we use nanoantennas (NAs) fabricated from multilayer TMDs, which allow complete flexibility with the choice of substrate due to the adhesive van der Waals forces, enabling high refractive index contrast or the use of highly reflective metallic surfaces. We demonstrate the localized formation of SPEs in WSe$_2$ monolayers transferred onto WS$_2$ NAs on both SiO$_2$ and Au substrates, enabling strong photonic enhancements and increased single photon collection. We provide evidence for enhanced quantum efficiencies (QE) reaching an average value of 43% (7%) for SPEs on WS$_2$ NAs on a SiO$_2$ (Au) substrate. We further combine the advantages offered by both dielectric and metallic substrates to numerically simulate an optimized NA geometry for maximum WSe$_2$ single photon excitation, emission, collection. Thus, the fluorescence is enhanced by a factor of over 4 orders of magnitude compared to vacuum and 5 orders of magnitude compared to a flat SiO$_2$/Si surface. Our work showcases the advantages offered by employing TMD material nanoresonators on various substrates for SPE formation and photonic enhancement.

cond-mat.mes-hall

Realization of Z$_2$ topological photonic insulators made from multilayer transition metal dichalcogenides

Monolayers of semiconducting transition metal dichalcogenides (TMDs) have long attracted interest for their intriguing optical and electronic properties. Recently TMDs in their quasi-bulk form have started to show considerable promise for nanophotonics thanks to their high refractive indices, large optical anisotropy, wide transparency windows reaching to the visible, and robust room temperature excitons promising for nonlinear optics. Adherence of TMD layers to any substrate via van der Waals forces is a further key enabler for nanofabrication of sophisticated photonic structures requiring heterointegration. Here, we capitalize on these attractive properties and realize topological spin-Hall photonic lattices made of arrays of triangular nanoholes in 50 to 100 nm thick WS$_2$ flakes exfoliated on SiO$_2$/Si substrates. High quality structures are achieved taking advantage of anisotropic dry etching dictated by the crystal axes of WS$_2$. Reflectance measurements at room temperature show a photonic gap opening in the near-infrared in trivial and topological phases. Unidirectional propagation along the domain interface is demonstrated in real space via circularly polarized laser excitation in samples with both zigzag and armchair domain boundaries. Finite-difference time-domain simulations are used to interpret optical spectroscopy results. Our work opens the way for future sophisticated nanophotonic devices based on the layered (van der Waals) materials platform.

physics.optics

Van der Waals Nanoantennas on Gold as Hosts for Hybrid Mie-Plasmonic Resonances

Dielectric nanoresonators have been shown to circumvent the heavy optical losses associated with plasmonic devices, however they suffer from less confined resonances. By constructing a hybrid system of both dielectric and metallic materials, one can retain the low losses of dielectric resonances, whilst gaining additional control over the tuning of the modes with the metal, and achieving stronger mode confinement. In particular, multi-layered van der Waals materials are emerging as promising candidates for integration with metals owing to their weak attractive forces, which enable deposition onto such substrates without the requirement of lattice matching. Here we use layered, high refractive index WS$_2$ exfoliated on gold, to fabricate and optically characterize a hybrid nanoantenna-on-gold system. We experimentally observe a hybridization of Mie resonances, Fabry-Pérot modes, and surface plasmon-polaritons launched from the nanoantennas into the substrate. We achieve experimental quality factors of Mie-plasmonic modes of up to 20 times that of Mie resonances in nanoantennas on silica, and observe signatures of a supercavity mode with a Q factor of 263 $\pm$ 28, resulting from strong mode coupling between a higher-order anapole and Fabry-Pérot-plasmonic mode. We further simulate WS$_2$ nanoantennas on gold with an hBN spacer, resulting in calculated electric field enhancements exceeding 2600, and a Purcell factor of 713. Our results demonstrate dramatic changes in the optical response of dielectric nanophotonic structures placed on gold, opening new possibilities for nanophotonics and sensing with simple-to-fabricate devices.

cond-mat.mes-hall

Van der Waals Materials for Applications in Nanophotonics

Numerous optical phenomena and applications have been enabled by nanophotonic structures. Their current fabrication from high refractive index dielectrics, such as silicon or gallium phosphide, pose restricting fabrication challenges, while metals, relying on plasmons and thus exhibiting high ohmic losses, limit the achievable applications. Here, we present an emerging class of layered so-called van der Waals (vdW) crystals as a viable nanophotonics platform. We extract the dielectric response of 11 mechanically exfoliated thin-film (20-200 nm) van der Waals crystals, revealing high refractive indices up to n = 5, pronounced birefringence up to $Δ$n = 3, sharp absorption resonances, and a range of transparency windows from ultraviolet to near-infrared. We then fabricate nanoantennas on SiO$_2$ and gold utilizing the compatibility of vdW thin films with a variety of substrates. We observe pronounced Mie resonances due to the high refractive index contrast on SiO$_2$ leading to a strong exciton-photon coupling regime as well as largely unexplored high-quality-factor, hybrid Mie-plasmon modes on gold. We demonstrate further vdW-material-specific degrees of freedom in fabrication by realizing nanoantennas from stacked twisted crystalline thin-films, enabling control of nonlinear optical properties, and post-fabrication nanostructure transfer, important for nano-optics with sensitive materials.

physics.optics

Probing Electronic States in Monolayer Semiconductors through Static and Transient Third-Harmonic Spectroscopy

Electronic states and their dynamics are of critical importance for electronic and optoelectronic applications. Here, we probe various relevant electronic states in monolayer MoS2, such as multiple excitonic Rydberg states and free-particle energy bands, with a high relative contrast of up to >200 via broadband (from ~1.79 to 3.10 eV) static third-harmonic spectroscopy, which is further supported by theoretical calculations. Moreover, we introduce transient third-harmonic spectroscopy to demonstrate that third-harmonic generation can be all-optically modulated with a modulation depth exceeding ~94% at ~2.18 eV, providing direct evidence of dominant carrier relaxation processes, associated with carrier-exciton and carrier-phonon interactions. Our results indicate that static and transient third-harmonic spectroscopies are not only promising techniques for the characterization of monolayer semiconductors and their heterostructures, but also a potential platform for disruptive photonic and optoelectronic applications, including all-optical modulation and imaging.

physics.optics

Lattice dynamics, phonon chirality and spin-phonon coupling in 2D itinerant ferromagnet Fe3GeTe2

Fe3GeTe2 has emerged as one of the most fascinating van der Waals crystals due to its two-dimensional (2D) itinerant ferromagnetism, topological nodal lines and Kondo lattice behavior. However, lattice dynamics, chirality of phonons and spin-phonon coupling in this material, which set the foundation for these exotic phenomena, have remained unexplored. Here we report the first experimental investigation of the phonons and mutual interactions between spin and lattice degrees of freedom in few-layer Fe3GeTe2. Our results elucidate three prominent Raman modes at room temperature: two A1g(Γ) and one E2g(Γ) phonons. The doubly degenerate E2g(Γ) mode reverses the helicity of incident photon, indicating the pseudo-angular momentum and chirality. Through analysis of temperature-dependent phonon energies and lifetimes, which strongly diverge from the anharmonic model below Curie temperature, we determine the spin-phonon coupling in Fe3GeTe2. Such interaction between lattice oscillations and spin significantly enhances the Raman susceptibility, allowing us to observe two additional Raman modes at the cryogenic temperature range. In addition, we reveal laser radiation induced degradation of Fe3GeTe2 in ambient conditions and the corresponding Raman fingerprint. Our results provide the first experimental analysis of phonons in this novel 2D itinerant ferromagnet and their applicability for further fundamental studies and application development.

cond-mat.mes-hall