arXiv subjects

Battulga Munkhbat

Publications and source records attributed to Battulga Munkhbat.

30 records · Page 2Linked to original sources

arXiv2023

Probing optical anapoles with fast electron beams

Optical anapoles are intriguing charge-current distributions characterized by a strong suppression of electromagnetic radiation. They originate from the destructive interference of the radiation produced by electric and toroidal multipoles. Although anapoles in dielectric structures have been probed and mapped with a combination of near- and far-field optical techniques, their excitation using fast electron beams has not been explored so far. Here, we theoretically and experimentally analyze the excitation of optical anapoles in tungsten disulfide (WS$_2$) nanodisks using Electron Energy Loss Spectroscopy (EELS) in Scanning Transmission Electron Microscopy (STEM). We observe prominent dips in the electron energy loss spectra and associate them with the excitation of optical anapoles and anapole-exciton hybrids. We are able to map the anapoles excited in the WS$_2$ nanodisks with subnanometer resolution and find that their excitation can be controlled by placing the electron beam at different positions on the nanodisk. Considering current research on the anapole phenomenon, we envision EELS in STEM to become a useful tool for accessing optical anapoles appearing in a variety of dielectric nanoresonators.

physics.optics↗

arXiv2022

Optical constants of several multilayer transition metal dichalcogenides measured by spectroscopic ellipsometry in the 300-1700 nm range: high-index, anisotropy, and hyperbolicity

Transition metal dichalcogenides (TMDs) attract significant attention due to their exceptional optical and excitonic properties. It was understood already in the 1960s, and recently rediscovered, that many TMDs possess high refractive index and optical anisotropy, which make them attractive for nanophotonic applications. However, accurate analysis and predictions of nanooptical phenomena require knowledge of dielectric constants along both in- and out-of-plane directions and over a broad spectral range -- information, which is often inaccessible or incomplete. Here, we present an experimental study of optical constants from several exfoliated TMD multilayers obtained using spectroscopic ellipsometry in the broad range of 300--1700 nm. The specific materials studied include semiconducting WS$_2$, WSe$_2$, MoS$_2$, MoSe$_2$, MoTe$_2$, as well as, in-plane anisotropic ReS$_2$, WTe$_2$, and metallic TaS$_2$, TaSe$_2$, and NbSe$_2$. The extracted parameters demonstrate high-index ($n$ up till $\approx 4.84$ for MoTe$_2$), significant anisotropy ($n_{\parallel}-n_{\perp} \approx 1.54$ for MoTe$_2$), and low absorption in the near infrared region. Moreover, metallic TMDs show potential for combined plasmonic-dielectric behavior and hyperbolicity, as their plasma frequency occurs at around $\sim$1000--1300 nm depending on the material. The knowledge of optical constants of these materials opens new experimental and computational possibilities for further development of all-TMD nanophotonics.

physics.optics↗

arXiv2022

Tunable critical Casimir forces counteract Casimir-Lifshitz attraction

Casimir forces in quantum electrodynamics emerge between microscopic metallic objects because of the confinement of the vacuum electromagnetic fluctuations occurring even at zero temperature. Their generalization at finite temperature and in material media are referred to as Casimir--Lifshitz forces. These forces are typically attractive, leading to the widespread problem of stiction between the metallic parts of micro- and nanodevices. Recently, repulsive Casimir forces have been experimentally realized but their reliance on specialized materials prevents their dynamic control and thus limits their further applicability. Here, we experimentally demonstrate that repulsive critical Casimir forces, which emerge in a critical binary liquid mixture upon approaching the critical temperature, can be used to actively control microscopic and nanoscopic objects with nanometer precision. We demonstrate this by using critical Casimir forces to prevent the stiction caused by the Casimir--Lifshitz forces. We study a microscopic gold flake above a flat gold-coated substrate immersed in a critical mixture. Far from the critical temperature, stiction occurs because of dominant Casimir--Lifshitz forces. Upon approaching the critical temperature, however, we observe the emergence of repulsive critical Casimir forces that are sufficiently strong to counteract stiction. This experimental demonstration can accelerate the development of micro- and nanodevices by preventing stiction as well as providing active control and precise tunability of the forces acting between their constituent parts.

cond-mat.soft↗

arXiv2022

Nanostructured transition metal dichalcogenide multilayers for advanced nanophotonics

Transition metal dichalcogenides (TMDs) attract significant attention due to their exceptional optical, excitonic, mechanical, and electronic properties. Nanostructured multilayer TMDs were recently shown to be highly promising for nanophotonic applications, as motivated by their exceptionally high refractive indexes and optical anisotropy. Here, we extend this vision to more sophisticated structures, such as periodic arrays of nanodisks and nanoholes, as well as proof-of-concept waveguides and resonators. We specifically focus on various advanced nanofabrication strategies, including careful selection of resists for electron beam lithography and etching methods. The specific materials studied here include semiconducting WS$_2$, in-plane anisotropic ReS$_2$, and metallic TaSe$_2$, TaS$_2$ and NbSe$_2$. The resulting nanostructures can potentially impact several nanophotonic and optoelectronic areas, including high-index nanophotonics, plasmonics and on-chip optical circuits. The knowledge of TMD material-dependent nanofabrication parameters developed here will help broaden the scope of future applications of these materials in all-TMD nanophotonics.

physics.optics↗

arXiv2020

Enhancing vibrational light-matter coupling strength beyond the molecular concentration limit using plasmonic arrays

Vibrational strong coupling is emerging as a promising tool to modify molecular properties, by making use of hybrid light-matter states known as polaritons. Fabry-Perot cavities filled with organic molecules are typically used, and the molecular concentration limits the maximum reachable coupling strength. Developing methods to increase the coupling strength beyond the molecular concentration limit are highly desirable. In this letter, we investigate the effect of adding a gold nanorod array into a cavity containing pure organic molecules, using FT-IR microscopy and numerical modeling. Incorporation of the plasmonic nanorod array, that acts as artificial molecules, leads to an order of magnitude increase in the total coupling strength for the cavity filled with organic molecules. Additionally, we observe a significant narrowing of the plasmon linewidth inside the cavity. We anticipate that these results will be a step forward in exploring vibropolaritonic chemistry and may be used in plasmon based bio-sensors.

physics.optics↗

arXiv2020

Casimir microcavities for tunable self-assembled polaritons

Hybrid light-matter states, polaritons, are one of the central concepts in modern quantum optics and condensed matter physics. Polaritons emerge as a result of strong interaction between an optical mode and a material resonance, which is frequently realized in molecular, van der Waals, or solid-state platforms (1-7). However, this route requires accurate (nano)fabrication and often lacks simple means for tunability, which could be disadvantageous in some applications. Here, we use a different approach to realize polaritonic states by employing a stable equilibrium between two parallel gold nanoflakes in an aqueous solution (8). Such plates form a self-assembled Fabry-Perot microcavity with the fundamental optical mode in the visible spectral range. The equilibrium distance between the plates is determined by a balance between attractive Casimir and repulsive electrostatic forces (9-11) and can be controlled by concentration of ligand molecules in the solution, temperature, and light pressure, which allows active and facile tuning of the cavity resonance by external stimuli. Using this Casimir approach, we demonstrate self-assembled polaritons by placing an excitonic medium in the microcavity region, as well as observe their laser-induced modulations in and out of the strong coupling regime. These Casimir microcavities can be used as sensitive and tunable polaritonic platforms for a variety of applications, including opto-mechanics (12), nanomachinery (13), and cavity-induced effects, like polaritonic chemistry (14).

physics.optics↗

arXiv2020

Transition metal dichalcogenide metamaterials with atomic precision

The ability to extract materials just a few atoms thick has led to discovery of graphene, monolayer transition metal dichalcogenides (TMDs), and other important two-dimensional materials. The next step in promoting understanding and utility of the flatland physics beyond the state-of-the-art is to study one-dimensional edges of such two-dimensional materials as well as to control the edge-plane ratio. Edges typically exhibit properties that are unique and distinctly different from those of planes and bulk. Thus, controlling them allows to design principally new materials with synthetic edge-plane-bulk characteristics, that is, TMD metamaterials. However, the enabling technology to study such metamaterials experimentally in a precise and systematic way has not yet been developed. Here we report a facile and controllable anisotropic wet etching method that allows scalable fabrication of TMD metamaterials with atomic precision. We show that TMDs can be etched along certain crystallographic axes, such that the obtained edges are atomically sharp and exclusively zigzag-terminated. This results in hexagonal nanostructures of predefined order and complexity, including few nanometer thin nanoribbons and nanojunctions. The method thus enables future studies of a broad range of TMD metamaterials with tailored functionality through atomically precise control of the structure.

physics.app-ph↗

arXiv2019

Ultrastrong coupling between nanoparticle plasmons and cavity photons at ambient conditions

Ultrastrong coupling is a distinct regime of electromagnetic interaction that enables a rich variety of intriguing physical phenomena. Traditionally, this regime has been reached by coupling intersubband transitions of multiple quantum wells, superconducting artificial atoms, or two-dimensional electron gases to microcavity resonators. However, employing these platforms requires demanding experimental conditions such as cryogenic temperatures, strong magnetic fields, and high vacuum. Here, we use plasmonic nanorods array positioned at the antinode of the resonant optical Fabry-Pérot microcavity to reach the ultrastrong coupling (USC) regime at ambient conditions and without the use of magnetic fields. From optical measurements we extract the value of the interaction strength over the transition energy as high as g/ω~0.55, deep in the USC regime, while the nanorods array occupies only ~4% of the cavity volume. Moreover, by comparing the resonant energies of the coupled and uncoupled systems, we indirectly observe up to ~10% modification of the ground-state energy, which is a hallmark of USC. Our results suggest that plasmon-microcavity polaritons are a promising new platform for room-temperature USC realizations in the optical and infrared range.

physics.optics↗

arXiv2019

Circular dichroism mode splitting and bounds to its enhancement with cavity-plasmon-polaritons

The ability to differentiate chiral molecules of different handedness is of great importance for chemical and life sciences. Since most of the relevant chiral molecules have their chiral transitions in the UV region, detecting their circular dichroism (CD) signal is associated with practical experimental challenges of performing optical measurements in that spectral range. To address this problem, here, we study the possibility of shifting CD signal of a model chiral medium by reaching the strong coupling regime with an optical microcavity. Specifically, we show that by strongly coupling chiral plasmonic nanoparticles to a non-chiral Fabry-Pérot microcavity one can imprint the hybrid mode splitting, the hallmark of strongly coupled systems, on the CD spectrum of the coupled system and thereby effectively shift the chiral resonance of the model system to lower energies. We first predict the effect using analytical transfer-matrix method as well as numerical finite-difference time-domain (FDTD) simulations. Furthermore, we confirm the validity of theoretical predictions in a proof-of-principle experiment involving chiral plasmonic nanoparticles coupled to a Fabry-Pérot microcavity.

physics.optics↗

arXiv2019

Visualizing plasmon-exciton polaritons at the nanoscale using electron microscopy

Polaritons are compositional light-matter quasiparticles that have recently enabled remarkable breakthroughs in quantum and nonlinear optics, as well as in material science. Despite the enormous progress, however, a direct nanometer-scale visualization of polaritons has remained an open challenge. Here, we demonstrate that plasmon-exciton polaritons, or plexcitons, generated by a hybrid system composed of an individual silver nanoparticle and a few-layer transition metal dichalcogenide can be spectroscopically mapped with nanometer spatial resolution using electron energy loss spectroscopy in a scanning transmission electron microscope. Our experiments reveal important insights about the coupling process, which have not been reported so far. These include nanoscale variation of Rabi splitting and plasmon-exciton detuning, as well as absorption-dominated extinction signals, which in turn provide the ultimate evidence for the plasmon-exciton hybridization in the strong coupling regime. These findings pioneer new possibilities for in-depth studies of polariton-related phenomena with nanometer spatial resolution.

physics.optics↗

arXiv2018

Transition metal dichalcogenide nanodisks as high-index dielectric Mie nanoresonators

Monolayer transition metal dichalcogenides (TMDCs) have recently been proposed as a unique excitonic platform for advanced optical and electronic functionalities. However, in spite of intense research efforts, it has been largely overlooked that, in addition to displaying rich exciton physics, TMDCs also possess a very high refractive index. This opens a possibility to utilize these materials for constructing resonant nanoantennas based on subwavelength geometrical modes. Here we show that nanodisks fabricated from exfoliated multilayer WS$_2$ support distinct Mie resonances and so-called anapole states that can be easily tuned in wavelength over the visible and near-infrared spectral range by varying the nanodisks' size and aspect ratio. We argue that the TMDC material anisotropy and the presence of excitons substantially enrich nanophotonics by complementing traditional approaches based on plasmonics and well-known high-index materials such as silicon. As a proof-of-concept, we demonstrate a novel regime of light-matter interaction, anapole-exciton polaritons, which we realize within a single WS$_2$ nanodisk. Our results thus suggest that nanopatterned TMDCs are promising materials for high-index nanophotonics applications with enriched functionalities and superior prospects.

physics.optics↗

arXiv2018

Suppression of photo-oxidation of organic chromophores by strong coupling to plasmonic nanoantennas

Intermixed light-matter quasiparticles - polaritons - possess unique optical properties owned to their compositional nature. These intriguing hybrid states have been extensively studied over the past decades in a wide range of realizations aiming at both basic science and emerging applications. However, recently it has been demonstrated that not only optical, but also material-related properties, such as chemical reactivity and charge transport, may be significantly altered in the strong coupling regime of light-matter interactions. Here, we show that a nanoscale system, comprised of a plasmonic nanoprism strongly coupled to excitons in J-aggregated form of organic chromophores, experiences modified excited state dynamics and therefore modified photo-chemical reactivity. Our experimental results reveal that photobleaching, one of the most fundamental photochemical reactions, can be effectively controlled and suppressed by the degree of plasmon-exciton coupling and detuning. In particular, we observe a 100-fold stabilization of organic dyes for the red-detuned nanoparticles. Our findings contribute to understanding of photochemical properties in the strong coupling regime and may find important implications for the performance and improved stability of optical devices incorporating organic dyes.

physics.optics↗