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Tomáš Šikola

Publications and source records attributed to Tomáš Šikola.

At least 19 recordsLinked to original sources

Time-resolved study of carbonization and growth of ultrathin 3C-SiC on Si(111) under ultra-high vacuum

The early-stage formation of silicon carbide (SiC) on Si(111) by ethylene exposure under ultra-high vacuum (UHV) was investigated to resolve the time-dependent chemical and morphological evolution of an ultrathin layer. Clean Si(111) substrates were exposed to C$_2$H$_4$ at 800 °C for 2 min to 4 h, and the surfaces followed by in-situ X-ray photoelectron spectroscopy (XPS) and ex-situ AFM, SEM, AES, SIMS and TEM. Si 2p and C 1s peak analysis shows the progressive conversion of elemental silicon into a carbidic Si-C phase, the SiC fraction overtaking the elemental component between 120 and 160 min and saturating near 80-81% beyond 180 min, leaving about 19-20% residual elemental silicon. Correlative SEM and AFM reveal a parallel morphological progression, from sparse isolated islands to a coalesced, near-continuous layer. AES depth profiling confirms carbon incorporated into the near-surface region rather than weakly adsorbed as contamination, assigning the islands to early SiC nuclei. TEM confirms the zinc-blende lattice and the presence of cubic silicon carbide (3C-SiC). Together, these results provide a time-resolved picture of SiC nucleation, coalescence and layer growth on Si(111), relevant to 3C-SiC heteroepitaxy, and can be utilized in the optimization of SiC/Si(111) templates for growth of III-nitride and other carbide systems on silicon (e.g. Mo$_2$C).

cond-mat.mtrl-sci↗

Lead nanoparticles, the deep-ultraviolet to near-infrared plasmonic platform

Among the other non-noble metals, lead (Pb) is a material of particular interest for plasmonic applications in the deep ultraviolet spectral region. However, experimental studies on its plasmonic performance have not yet been conducted. In this work, the dependence of the optical properties of spherical lead nanoparticles on their diameter is demonstrated. The plasmonic performance of chemically synthesized lead nanoparticles is evaluated at the single-particle level by means of a combination of scanning transmission electron microscopy and electron energy loss spectroscopy. Our findings demonstrate that these nanoparticles support localized surface plasmon resonances across the entire spectrum from near-infrared to deep-ultraviolet. This range was identified as the most extensive among all plasmonic elemental metals, extending to wavelengths below 200 nanometers. Consequently, lead nanoparticles exhibit stable plasmonic performance over a remarkably broad wavelength range, thereby substantiating their potential as a multispectral plasmonic platform.

physics.optics↗

Additive and Subtractive Color Filters Based on Birefringent Dielectric Metasurfaces

Dielectric metasurfaces offer a path to high-efficiency optical components at the sub-wavelength scale. In this work, we utilize the wavelength-dependent birefringence of TiO2 nanopillars to create transmissive color filters with switchable spectral responses. We demonstrate that the same physical nanostructure array can function as either an additive (band-pass) or a subtractive (band-stop) filter solely by rotating an external polarizer. The metasurface was fabricated via a modified damascene process, enabling high-aspect-ratio structures with spatial resolutions down to 250 nm. The filters achieve transmission efficiencies of 70% tailorable across the entire visible spectrum, avoiding the ohmic losses typical of plasmonic alternatives. This approach provides a tunable, high-efficiency platform offering a versatile and compact solution for next-generation high-resolution imaging systems.

physics.optics↗

Durable Enhancement of $\mathbf{MoS_2}$ Single-Layer Photoluminescence by Ultraviolet Laser Treatment Under Ambient Conditions

Single-layer molybdenum disulfide ($MoS_2$) possesses significant potential for nanoscale optoelectronics, but achieving high-intensity, long-term-stable photoluminescence (PL) emission remains a challenge. In this work, we demonstrate a remarkably robust, more than 8-fold maximum enhancement in the PL intensity of exfoliated and CVD-grown single-layer $MoS_2$ via a non-destructive ultraviolet (UV) laser treatment method. This substantial increase in radiative efficiency is accompanied by a trion-to-neutral exciton transition in the PL signal and a corresponding blue shift of the Raman $E_{2g}^1$ and $A_{1g}$ vibrational modes, signaling successful electron depletion (p-doping) and formation of Mo-O bonds, respectively. Furthermore, we demonstrate precise spatial control over PL properties by confining PL treatment exclusively to the UV laser-treated area. Crucially, the enhanced PL performance shows exceptional longevity; the CVD sample and the exfoliated sample remained stable for the entire monitoring period (72 and 32 days, respectively) under ambient conditions. We further investigated UV laser treatment in a controlled-environment chamber under argon, nitrogen, and oxygen atmospheres, distinguishing the influence of oxygen as the PL treatment agent. These findings establish a reliable pathway for the permanent treatment of single-layer $MoS_2$ PL properties, an essential step toward practical, high-performance nanophotonic devices.

cond-mat.mes-hall↗

Inverse designed full-Stokes polarimetric metasurface with simultaneous wavefront sensing for visible light

Metasurfaces have emerged as a powerful platform for compact optical sensors by replacing bulky lenses with flat arrays of subwavelength nanostructures. In precision optical metrology, the simultaneous mapping of a beam's polarization state and wavefront is crucial for real-time diagnostics of stress-induced birefringence and surface flatness. To achieve this in a compact footprint, existing metasurfaces typically partition their aperture into discrete zones, which inherently restricts the light-gathering efficiency and numerical aperture of the system. Here we demonstrate an inverse-designed metasurface that integrates full-Stokes polarimetry and Shack-Hartmann wavefront sensing within a single, continuous aperture in the visible spectrum. By leveraging an adjoint optimization approach to independently control the geometry and rotation of each nanostructure, we break the aperture-sharing paradigm and utilize the entire pixel area for all channels. When coupled with a shallow neural network to automate peak identification and correct for hardware non-idealities, our device yields a mean polarization reconstruction error of only 0.046 across 100 test states on the Poincaré sphere, while simultaneously maintaining the precise focal-spot tracking required for sensitive wavefront tilt detection. This work highlights the capacity of inverse design to generate multifunctional, non-intuitive flat optics that outperforms its traditional counterparts.

physics.optics↗

Controlled dewetting and phase transition hysteresis of VO2 nanostructures

As artificial intelligence continues to grow, so does the need for more efficient ways to process data. Besides moving from electronic to photonic circuits, a promising approach is to integrate phase-change materials. Vanadium dioxide (VO$_2$) exhibits an ultrafast, near-room-temperature phase transition, characterized by hysteresis and large optical modulation -- making it a promising candidate for short-term memories and for mimicking neural behavior in brain-like computing systems. While the hysteresis behavior of VO$_2$ has been well studied in thin films and nanostructures, practical control and device integration have been limited only to thin films. Here, we demonstrate control over the phase transitions of VO$_2$ nanocylinders via lithographic patterning, controlled crystallization, and controlled dewetting. Because nanostructures are easier to address and consume less power than films, the ability to fabricate them with tailored geometry and hysteresis properties directly on integrated platforms is a key step toward scalable, energy-efficient memory and neuromorphic photonic devices.

cond-mat.mes-hall↗

Work-Function-Resolved Imaging of Relaxation Oscillations and Chemical Spillover in CO Oxidation over Platinum Surfaces

Chemical waves of CO oxidation on platinum surfaces exhibit complex spatio-temporal self-oscillations, yet the local electronic mechanisms driving their propagation remain poorly understood under operando conditions. In this work, we combine operando scanning electron microscopy with frequency-modulated Kelvin probe force microscopy (FM-KPFM) to simultaneously map secondary electron contrast and local work-function variations during CO oxidation on Pt. By utilizing the KPFM tip as a localized sensor, we provide the first work-function-resolved imaging of reaction fronts, enabling an unambiguous physical assignment of CO- and oxygen-covered states. Our results demonstrate that the spillover process of chemical wave-the transition and expansion of adsorbate phases-is characterized by a pronounced temporal asymmetry and spatial heterogeneity transition thresholds. KPFM identifies a rapid onset of oxygen coverage followed by a gradual, diffuse relaxation back to the CO-covered state, indicative of relaxation-type oscillations even at low pressures (10^-2 Pa). Correlative reaction-diffusion simulations reproduce this wave morphology, confirming that the high-resolution work-function signal provides unique insights into the internal structure and kinetic heterogeneity of the working catalyst surface.

cond-mat.mtrl-sci↗

Plasmonics of non-noble metals

Localized surface plasmon resonances are self-sustained, collective oscillations of free electrons in metallic nanostructures. They have a wide range of applications. The most common plasmonic metals are noble metals, such as gold and silver. However, there are applications, such as surface-enhanced Raman spectroscopy, in which using non-noble metals is advantageous. This review summarizes the investigation of localized surface plasmons in non-noble metal nanoparticles, providing an overview of the plasmonic properties of non-noble metals. We cover the following metals: aluminium (Al), antimony (Sb), bismuth (Bi), chromium (Cr), copper (Cu), gallium (Ga), indium (In), lead (Pb), magnesium (Mg), molybdenum (Mo), nickel (Ni), potassium (K), selenium (Se), sodium (Na), tellurium (Te), tin (Sn), titanium (Ti), tungsten (W), and zinc (Zn). Our summary therefore compares the plasmonic properties of non-noble metals and briefly introduces their potential to the readers.

physics.optics↗

Reconfigurable plasmonic hot spots enabled by composite VO2-gold plasmonic antennas

We theoretically investigate the formation of electric and magnetic hot spots with reconfigurable plasmonic antennas. We consider three material systems offering different levels of reconfigurability: gold with the static response, vanadium dioxide which allows for ON/OFF switching, and composite gold-vanadium dioxide material platform which offers a possibility to switch between the electric and magnetic hot spot within a single antenna. Using bowtie and diabolo antennas as a case study, we evaluate optical response functions (scattering and absorption cross-sections, electric and magnetic field enhancement). We demonstrate that the composite material system brings, in addition to enhanced reconfigurability, also novel features of plasmonic antennas, such as strong optical absorption and a joint electric-magnetic hotspot.

physics.optics↗

Tuning of Localized Surface Plasmons in Vanadium Dioxide Nanoparticles via Size and Insulator-Metal Transition

Vanadium dioxide has been identified as a promising phase-changing material for use in tunable plasmonic devices. In this study, we present a comprehensive modal analysis of single-phase and multi-phase vanadium dioxide nanoparticles. In-situ high-resolution electron energy loss spectroscopy was utilized to experimentally resolve the dipole plasmon peak, higher-order and breathing plasmonic modes, and bulk losses as a function of nanoparticle size. Furthermore, the focus is directed toward capturing the dynamic nanoscale optical response throughout the metal-insulator transition in a vanadium dioxide nanoparticle. This system possesses the ability to be gradually switched on and off in terms of the emergence of near-infrared plasmonic absorption. The switching is accompanied by a gradual spectral shift of the absorption peak, amounting to 0.18 eV for a 120 nm nanoparticle. It is envisioned that this phenomenon can be generalized to larger nanostructures with a higher aspect ratio, thereby introducing a wider tunability of the system, which is essential for functional nanodevices based on vanadium dioxide.

physics.optics↗

Establishing a library of metasurface building blocks through coherence-controlled holographic microscopy

Digital holographic microscopy is a powerful tool for characterizing transparent and reflective phase objects. Its ability to reconstruct amplitude and phase can also offer great insight into wavefront shaping and design of all-dielectric optical metasurfaces. While metasurfaces have reached widespread popularity, their design is often based purely on the results of numerical simulations which can overlook many of the real-world fabrication imperfections. Being able to verify the real phase response of a fabricated device is of great utility for high-performance devices. Here, we use holographic microscopy to validate metalibraries of rectangular TiO2 and Si building blocks. Illumination effects are studied for wavelengths from 600 to 740 nm and linear polarization rotating within the full range of unique states (0 to 180deg). Finally, by varying the numerical aperture of the condenser lens from 0.05 to 0.5 we also study the effects of an off-axis illumination. Comparing the experimental results with simulations from finite-difference time-domain and rigorous coupled-wave analysis, we highlight the limitations of these theoretical predictions and underscore the utility of an experimentally established library of building blocks. We demonstrate that our proposed method of holographic microscopy is both practical and effective for creating a metalibrary that accounts for all fabrication and material imperfections, which is crucial for designing high-efficiency metasurfaces.

physics.optics↗

Charge reservoir as a design concept for plasmonic antennas

Plasmonic antennas exploit localized surface plasmons to shape, confine, and enhance electromagnetic fields with subwavelength resolution. The field enhancement is contributed to by various effects, such as the inherent surface localization of plasmons or the plasmonic lightning-rod effect. Inspired by nanofocusing observed for propagating plasmons, we test the hypothesis that plasmonic antennas with a large cross-section represent a large charge reservoir, enabling large induced charge and field enhancement. Our study reveals that a large charge reservoir is accompanied by large radiative losses, which are the dominant factor, resulting in a low field enhancement.

physics.optics↗

Mass-transport-limited reaction rates and molecular diffusion in the van der Waals gap beneath graphene

The confinement of molecules within the van der Waals (vdW) gap between a two-dimensional 2D material and a catalytic substrate offers a promising route toward the development of molecule-selective catalysts with increased reaction rates. However, identifying the kinetic limitations of such confined reactions remains challenging. Here, we employ an inverted wedding-cake configuration of multilayer graphene on platinum to study the dynamics of graphene etching in the vdW gap by various molecules (O2, H2, and CO), using in situ scanning electron microscopy. Under the experimental conditions explored (up to p = 1.4x10-3 Pa and T = 1000 °C), the etching reaction rates are limited by mass transport within the confined space. This limitation persists even for CO, despite its anomalously enhanced transport resulting from a significant lifting of the vdW gap. Reactive molecular dynamics simulations further reveal multiple etching pathways for CO, enabled by confinement within the vdW space. Once mass-transport limitations are overcome, the vdW gap acts as an effective nanoreactor, facilitating reaction pathways that would be otherwise inaccessible on a pristine surface without spatial confinement.

cond-mat.mes-hall↗

Plasmonic properties of individual bismuth nanoparticles

Bismuth nanoparticles are being investigated due to their reported photothermal and photocatalytic properties. In this study, we synthesised spherical bismuth nanoparticles (50-600 nm) and investigated their structural and optical properties at the single particle level using analytical transmission electron microscopy. Our experimental results, supported by numerical simulations, demonstrate that bismuth nanoparticles support localised surface plasmon resonances, which can be tuned from the near-infrared to the ultraviolet spectral region by changing the nanoparticle size. Furthermore, plasmonic resonances demonstrate stability across the entire spectral bandwidth, enhancing the attractiveness of bismuth nanoparticles for applications over a wide spectral range. Bismuth's lower cost, biocompatibility, and oxidation resistance make it a suitable candidate for utilisation, particularly in industrial and large-scale plasmonic applications.

physics.optics↗

Graphene Enhanced Resonant Raman Spectroscopy of Gallium Nitride Nanocrystals

The scattering of lattice excitations (phonons) with the photoexcited charge carriers is of a major concern in optoelectronic devices. Here, the resonant Raman scattering will be utilized to study an exciton-phonon interaction in GaN nanocrystals, further enhanced by the underlying graphene. Raman spectroscopy using various excitation energies shows how the exciton-phonon interaction behaves, unveiling the scattering strength. The origin of the interaction is in the condition of resonance, which is directly observed in the temperature resolved spectra. Most importantly, the underlying graphene strongly enhances the coupling of phonons and excitons. Consequently, an enhanced resonant Raman spectrum of GaN nanocrystals possessing clearly observable phonon overtones up to the 4th order has been obtained. It has been demonstrated that the responsible effect is the electron transfer between nanocrystals and the underlying graphene. The utilization of such an increased coupling effect can be beneficial for a study of the charge carrier scattering in semiconducting nanomaterials, analysis of their crystal quality, improvement of sensor sensitivity and in the subsequent development of new-generation optoelectronic devices.

cond-mat.mes-hall↗

Bismuth plasmonic antennas

Bismuth is a particularly promising alternative plasmonic metal because of its theoretically predicted wide spectral bandwidth. In this study, we experimentally demonstrated the correlation between the shape and size of individual bismuth plasmonic antennas and their optical properties. To this end, we employed a combination of scanning transmission electron microscopy and electron energy loss spectroscopy. Bar-shaped and bowtie bismuth plasmonic antennas of various sizes were fabricated by focused ion beam lithography of a polycrystalline bismuth thin film. Our experimental findings demonstrate that these antennas support localised surface plasmon resonances and their dipole modes can be tuned through their size from the near-infrared to the entire visible spectral region. Furthermore, our findings demonstrate that bismuth exhibits a plasmon dispersion relation that is nearly identical to that of gold while maintaining its plasmonic performance even at higher plasmon energies, thus rendering it a promising low-cost alternative to gold.

physics.optics↗

Casimir-like effect driven self-assembly of graphene on molten metals

Casimir effect, explained by Hendrik Casimir in 1948, is a macroscopic manifestation of quantum electrodynamics. Symmetry breaking due to space confinement of vacuum fluctuations in between two planar mirrors results in an attractive force acting between the two mirrors. Here, we show that spontaneous self-assembly of two-dimensional (2D) layered materials grown on molten metals (rheotaxy) is driven by the mechanical forces exerted by the liquid on the graphene domain and that these forces are subject to a Casimir-like effect. We present in situ environmental and ultrahigh vacuum scanning electron microscopy observations of chemical vapor deposition of graphene on both solid and molten gold and copper, which reveal that the self-assembly occurs via translational and rotational motions of graphene domains during growth on molten metals. Using high-temperature (~ 1300 K) atomic force microscopy measurements of graphene/molten-metal interfaces, coupled with density functional theory and continuum modelling of 2D layers floating on a liquid surface, we attribute the observed phenomena to Casimir-like effect of surface undulations and give further guidance for achieving seamless stitching of 2D layer domains into large scale monolayers.

cond-mat.mes-hall↗

Achieving Different Stoichiometries and Morphologies in Vapor Phase Deposition of Inorganic Halide Perovskites: Single or Dual Precursor Sources?

Inorganic halide perovskites have become attractive for many optoelectronic applications due to their outstanding properties. While chemical synthesis techniques have been successful in producing high-quality perovskite crystals, scaling up to wafer-scale thin films remains challenging. Vapor deposition methods, particularly physical vapor deposition and chemical vapor deposition, have emerged as potential solutions for large-scale thin film fabrication. However, the control of phase purity during deposition remains problematic. Here, we investigate single-source (CsPbBr3) and dual-source (CsBr and PbBr2) vapor deposition techniques to achieve phase-pure CsPbBr3 thin films. Utilizing Knudsen Effusion Mass Spectrometry, we demonstrate that while the single-source CsPbBr3 evaporation is partially congruent, it leads to compositional changes in the evaporant over time. The dual-source evaporation, with a precise control of the PbBr2/CsBr flux ratio, can improve phase purity, particularly at elevated substrate temperatures at excess PbBr2 conditions. Our results give direct evidence that the growth is CsBr-limited. Overall, our findings provide critical insights into the vapor phase deposition processes, highlighting the importance of evaporation conditions in achieving the desired inorganic perovskite stoichiometry and morphology.

cond-mat.mtrl-sci↗