arXiv subjects

Y. K. Kato

Publications and source records attributed to Y. K. Kato.

At least 19 recordsLinked to original sources

arXiv2026

Trion transfer in mixed-dimensional heterostructures

Charged excitons, or trions, offering unique spin and charge degrees of freedom, have primarily been investigated in doped systems where charges are long considered indispensable. Here, we present an alternative route to ultra-efficient trion emission from an intrinsic, defect-free semiconductor via a transfer mechanism. By exciting trions in two-dimensional tungsten-diselenide donors and transferring them into one-dimensional carbon-nanotube acceptors in mixed-dimensional heterostructures, we circumvent the usual carrier requirement, overcoming intrinsic Auger-quenching limitations. Benefitting from a reservoir effect induced by dimensional heterogeneity, this process achieves trion emission efficiencies increased by over 100-fold compared to conventional doping-based approaches, and remains robust across diverse doping conditions. Our findings extend the exciton transfer paradigm to the three-body quasiparticles, offering a new platform for advancing excitonic physics and trion-based optoelectronic/spintronic applications.

cond-mat.mes-hall↗

arXiv2025

Dielectric environment engineering via 2D material heterostructure formation on hybrid photonic crystal nanocavity

Hybrid integration of two-dimensional (2D) materials with nanophotonic platforms has enabled compact optoelectronic devices by leveraging the unique optical and electronic properties of atomically thin layers. While most efforts have focused on coupling 2D materials to pre-defined photonic structures, the broader potential of 2D heterostructures for actively engineering the photonic environment remains largely unexplored. In our previous work, we employed single types of 2D material and showed that even monolayer flakes can locally induce high-$Q$ nanocavities in photonic crystal (PhC) waveguides through effective refractive index modulation. Here, we extend this concept by demonstrating that further transferring of 2D material flakes onto the induced hybrid nanocavity to form heterostructures enable more flexibility for post-fabrication dielectric environment engineering of the cavity. We show that the high-$Q$ hybrid nanocavities remain robust under sequential flake stacking. Coupling optically active MoTe$_{2}$ flake to these cavities yields enhanced photoluminescence and reduced emission lifetimes, consistent with Purcell-enhanced light-matter interactions. Additionally, encapsulation with a top hBN layer leads to a significant increase in the cavity $Q$ factor, in agreement with numerical simulations. Our results show that these heterostructure stacks not only preserve the cavity quality but also introduce an additional degrees of control -- via flake thickness, refractive indices, size and interface design -- offering a richer dielectric environment modulation landscape than what is achievable with monolayers alone, providing a versatile method toward scalable and reconfigurable hybrid nanophotonic systems.

physics.optics↗

arXiv2023

Self-aligned hybrid nanocavities using atomically thin materials

Two-dimensional (2D) van der Waals layered materials with intriguing properties are increasingly being adopted in hybrid photonics. The 2D materials are often integrated with photonic structures including cavities to enhance light-matter coupling, providing additional control and functionality. The 2D materials, however, needs to be precisely placed on the photonic cavities. Furthermore, the transfer of 2D materials onto the cavities could degrade the cavity quality $(Q)$ factor. Instead of using prefabricated PhC nanocavities, we demonstrate a novel approach to form a hybrid nanocavity by partially covering a PhC waveguide post-fabrication with a suitably-sized 2D material flake. We successfully fabricated such hybrid nanocavity devices with hBN, WSe$_2$ and MoTe$_2$ flakes on silicon PhC waveguides, obtaining $Q$ factors as high as $4.0\times10^5$. Remarkably, even mono- and few-layer flakes can provide sufficient local refractive index modulation to induce nanocavity formation. Since the 2D material is spatially self-aligned to the nanocavity, we have also managed to observe cavity PL enhancement in a MoTe$_2$ hybrid cavity device, with a cavity Purcell enhancement factor of about 15. Our results highlights the prospect of using such 2D materials-induced PhC nanocavity to realize a wide range of photonic components for hybrid devices and integrated photonic circuits.

physics.optics↗

arXiv2023

Room-temperature quantum emission from interface excitons in mixed-dimensional heterostructures

The development of van der Waals heterostructures has introduced unconventional phenomena that emerge at atomically precise interfaces. For example, interlayer excitons in two-dimensional transition metal dichalcogenides show intriguing optical properties at low temperatures. Here we report on room-temperature observation of interface excitons in mixed-dimensional heterostructures consisting of two-dimensional tungsten diselenide and one-dimensional carbon nanotubes. Bright emission peaks originating from the interface are identified, spanning a broad energy range within the telecommunication wavelengths. The effect of band alignment is investigated by systematically varying the nanotube bandgap, and we assign the new peaks to interface excitons as they only appear in type-II heterostructures. Room-temperature localization of low-energy interface excitons is indicated by extended lifetimes as well as small excitation saturation powers, and photon correlation measurements confirm single-photon emission. With mixed-dimensional van der Waals heterostructures where band alignment can be engineered, new opportunities for quantum photonics are envisioned.

cond-mat.mes-hall↗

arXiv2023

Resonant exciton transfer in mixed-dimensional heterostructures for overcoming dimensional restrictions in optical processes

Nanomaterials exhibit unique optical phenomena, in particular excitonic quantum processes occurring at room temperature. The low dimensionality, however, imposes strict requirements for conventional optical excitation, and an approach for bypassing such restrictions is desirable. Here we report on exciton transfer in carbon-nanotube/tungsten-diselenide heterostructures, where band alignment can be systematically varied. The mixed-dimensional heterostructures display a pronounced exciton reservoir effect where the longer-lifetime excitons within the two-dimensional semiconductor are funneled into carbon nanotubes through diffusion. This new excitation pathway presents several advantages, including larger absorption areas, broadband spectral response, and polarization-independent efficiency. When band alignment is resonant, we observe substantially more efficient excitation via tungsten diselenide compared to direct excitation of the nanotube. We further demonstrate simultaneous bright emission from an array of carbon nanotubes with varied chiralities and orientations. Our findings show the potential of mixed-dimensional heterostructures and band alignment engineering for energy harvesting and quantum applications through exciton manipulation.

cond-mat.mes-hall↗

arXiv2022

Quantization of mode shifts in nanocavities integrated with atomically thin sheets

The unique optical properties of two-dimensional layered materials are attractive for achieving increased functionality in integrated photonics. Owing to the van der Waals nature, these materials are ideal for integrating with nanoscale photonic structures. Here we report on carefully designed air-mode silicon photonic crystal nanobeam cavities for efficient control through two-dimensional materials. By systematically investigating various types and thickness of two-dimensional materials, we are able to show that enhanced responsivity allows for giant shifts of the resonant wavelength. With atomically precise thickness over a macroscopic area, few-layer flakes give rise to quantization of the mode shifts. We extract the dielectric constant of the flakes and find that it is independent of the layer number down to a monolayer. Flexible reconfiguration of a cavity is demonstrated by stacking and removing ultrathin flakes. With an unconventional cavity design, our results open up new possibilities for photonic devices integrated with two-dimensional materials.

physics.optics↗

arXiv2021

Universal map of gas-dependent kinetic selectivity in carbon nanotube growth

Single-walled carbon nanotubes have been a candidate for outperforming silicon in ultrascaled transistors, but the realization of nanotube-based integrated circuits requires dense arrays of purely semiconducting species. Control over kinetics and thermodynamics in tube-catalyst systems plays a key role for direct growth of such nanotube arrays, and further progress requires the comprehensive understanding of seemingly contradictory reports on the growth kinetics. Here, we propose a universal kinetic model and provide its quantitative verification by ethanol-based isotope labeling experiments. While the removal of carbon from catalysts dominates the growth kinetics under a low supply of precursors, our kinetic model and experiments demonstrate that chirality-dependent growth rates emerge when sufficient amounts of carbon and etching agents are co-supplied. As the model can be extended to create kinetic maps as a function of gas compositions, our findings resolve discrepancies in literature and offer rational strategies for chirality selective growth for practical applications.

physics.app-ph↗

arXiv2021

Chiral modes near exceptional points in symmetry broken H1 photonic crystal cavities

The H1 photonic crystal cavity supports two degenerate dipole modes of orthogonal linear polarization which could give rise to circularly polarized fields when driven with a $π$/$2$ phase difference. However, fabrication errors tend to break the symmetry of the cavity which lifts the degeneracy of the modes, rendering the cavity unsuitable for supporting circular polarization. We demonstrate numerically, a scheme that induces chirality in the cavity modes, thereby achieving a cavity that supports intrinsic circular polarization. By selectively modifying two air holes around the cavity, the dipole modes could interact via asymmetric coherent backscattering which is a non-Hermitian process. With suitable air hole parameters, the cavity modes approach the exceptional point, coalescing in frequencies and linewidths as well as giving rise to significant circular polarization close to unity. The handedness of the chirality can be selected depending on the choice of the modified air holes. Our results highlight the prospect of using the H1 photonic crystal cavity for chiral-light matter coupling in applications such as valleytronics, spin-photon interfaces and the generation of single photons with well-defined spins.

physics.optics↗

arXiv2021

Formation of Organic Color Centers in Air-Suspended Carbon Nanotubes Using Vapor-Phase Reaction

Organic color centers in single-walled carbon nanotubes have demonstrated exceptional ability to generate single photons at room temperature in the telecom range. Combining the color centers with pristine air-suspended tubes would be desirable for improved performance, but all current synthetic methods occur in solution which makes them incompatible. Here we demonstrate formation of color centers in air-suspended nanotubes using vapor-phase reaction. Functionalization is directly verified on the same nanotubes by photoluminescence spectroscopy, with unambiguous statistics from more than a few thousand individual nanotubes. The color centers show a strong diameter-dependent emission intensity, which can be explained with a theoretical model for chemical reactivity taking into account strain along the tube curvature. We are also able to estimate the defect density by comparing the experiments with simulations based on a one-dimensional diffusion equation, whereas the analysis of diameter dependent peak energies gives insight to the nature of the dopant states. Time-resolved measurements show a longer lifetime for color center emission compared to E$_{11}$ exciton states. Our results highlight the influence of the tube structure on vapor-phase reactivity and emission properties, providing guidelines for development of high-performance near-infrared quantum light sources.

cond-mat.mtrl-sci↗

arXiv2021

Near-unity radiative quantum efficiency of excitons in carbon nanotubes

The efficiencies of photonic devices are primarily governed by radiative quantum efficiency, which is a property given by the light emitting material. Quantitative characterization for carbon nanotubes, however, has been difficult despite being a prominent material for nanoscale photonics. Here we determine the radiative quantum efficiency of bright excitons in carbon nanotubes by modifying the exciton dynamics through cavity quantum electrodynamical effects. Silicon photonic crystal nanobeam cavities are used to induce the Purcell effect on individual carbon nanotubes. Spectral and temporal behavior of the cavity enhancement is characterized by photoluminescence microscopy, and the fraction of the radiative decay process is evaluated. We find that the radiative quantum efficiency is near unity for bright excitons in carbon nanotubes at room temperature.

cond-mat.mes-hall↗

arXiv2021

Waveguide coupled cavity-enhanced light emission from individual carbon nanotubes

We demonstrate an individual single-walled carbon nanotube light emitter integrated onto a microcavity and a waveguide operating in the telecom wavelength regime. Light emission from the carbon nanotube is enhanced at the cavity resonance and is efficiently extracted from the waveguide facet. We have transferred carbon nanotubes to a nanobeam cavity with a dry process, ensuring that an individual carbon nanotube is used. The guided light emission from a chirality-identified single carbon nanotube has a narrow linewidth of less than 1.3 nm and an off-resonance rejection of $\sim$17 dB. The waveguide-coupled device configuration is compatible with fully integrated on-chip designs and is promising for carbon-nanotube-based photonics.

physics.optics↗

arXiv2020

Deterministic transfer of optical-quality carbon nanotubes for atomically defined technology

When continued device scaling reaches the ultimate limit imposed by atoms, technology based on atomically precise structures is expected to emerge. Device fabrication will then require building blocks with identified atomic arrangements and assembly of the components without contamination. Here we report on a versatile dry transfer technique for deterministic placement of optical-quality carbon nanotubes. Single-crystalline anthracene is used as a medium which readily sublimes by mild heating, leaving behind clean nanotubes and thus enabling bright photoluminescence. We are able to position nanotubes of a desired chirality with a sub-micron accuracy under in-situ optical monitoring, thereby demonstrating deterministic coupling of a nanotube to a photonic crystal nanobeam cavity. A cross junction structure is also designed and constructed by repeating the nanotube transfer, where intertube exciton transfer is observed. Our results represent an important step towards development of devices consisting of atomically precise components and interfaces.

cond-mat.mes-hall↗

arXiv2020

Hexagonal boron nitride as an ideal substrate for carbon nanotube photonics

Hexagonal boron nitride is widely used as a substrate for two-dimensional materials in both electronic and photonic devices. Here, we demonstrate that two-dimensional hexagonal boron nitride is also an ideal substrate for one-dimensional single-walled carbon nanotubes. Nanotubes directly attached to hexagonal boron nitride show bright photoluminescence with narrow linewidth at room temperature, comparable to air-suspended nanotubes. Using photoluminescence excitation spectroscopy, we unambiguously assign the chiralities of nanotubes on boron nitride by tracking individual tubes before and after contact with boron nitride. Although hexagonal boron nitride has a low dielectric constant and is attached to only one side of the nanotubes, we observe that optical transition energies are redshifted as much as ~50 meV from the air-suspended nanotubes. We also perform statistical measurements on more than 400 tubes, and the redshifts are found to be dependent on tube diameter. This work opens up new possibilities for all-solid-state carbon nanotube photonic devices by utilizing hexagonal boron nitride substrates.

cond-mat.mes-hall↗

arXiv2019

High efficiency dark-to-bright exciton conversion in carbon nanotubes

We report that dark excitons can have a large contribution to the emission intensity in carbon nanotubes due to an efficient exciton conversion from a dark state to a bright state. Time-resolved photoluminescence measurements are used to investigate decay dynamics and diffusion properties of excitons, and we obtain intrinsic lifetimes and diffusion lengths of bright excitons as well as diffusion coefficients for both bright and dark excitons. We find that the dark-to-bright transition rates can be considerably high, and that more than half of the dark excitons can be transformed into the bright excitons. The state transition rates have a large chirality dependence with a family pattern, and the conversion efficiency is found to be significantly enhanced by adsorbed air molecules on the surface of the nanotubes. Our findings show the nontrivial significance of the dark excitons on the emission kinetics in low dimensional materials, and demonstrate the potential for engineering the dark-to-bright conversion process by using surface interactions.

cond-mat.mes-hall↗

arXiv2019

Super-Resolution Fluorescence Imaging of Carbon Nanotubes Using a Nonlinear Excitonic Process

Highly efficient exciton-exciton annihilation process unique to one-dimensional systems is utilized for super-resolution imaging of air-suspended carbon nanotubes. Through the comparison of fluorescence signals in linear and sublinear regimes at different excitation powers, we extract the efficiency of the annihilation processes using conventional confocal microscopy. Spatial images of the annihilation rate of the excitons have resolution beyond the diffraction limit. We investigate excitation power dependence of the annihilation processes by experiment and Monte Carlo simulation, and the resolution improvement of the annihilation images can be quantitatively explained by the superlinearity of the annihilation process. We have also developed another method in which the cubic dependence of the annihilation rate on exciton density is utilized to achieve further sharpening of single nanotube images.

cond-mat.mes-hall↗

arXiv2018

Organic molecular tuning of many-body interaction energies in air-suspended carbon nanotubes

We investigate adsorption effects of copper phthalocyanine molecules on excitons and trions in air-suspended carbon nanotubes. Using photoluminescence excitation spectroscopy, we observe that exciton energy redshifts gradually with the molecular deposition thickness. The trion emission is also observed at large deposition amounts, which indicates charge transfer between the phthalocyanine molecules and carbon nanotubes. Analysis of the spectra for individual tubes reveal a correlation between the exciton-trion energy separation and the exciton emission energy, showing that the many-body interaction energies scale similarly with the molecular dielectric screening.

cond-mat.mes-hall↗

arXiv2018

Molecular screening effects on exciton-carrier interactions in suspend carbon nanotubes

Photoluminescence spectroscopy measurements are performed on suspended carbon nanotubes in a field-effect configuration, and the gate voltage dependence of photoluminescence spectra are compared for the pristine and the molecularly adsorbed states of the nanotubes. We quantify the molecular screening effect on the trion binding energies by determining the energy separation between the bright exciton and the trion emission energies for the two states. The voltage dependence shows narrower voltage regions of constant photoluminescence intensity for the adsorbed states, consistent with a reduction in the electronic bandgap due to screening effects. The charge neutrality points are found to shift after molecular adsorption, which suggests changes in the nanotube chemical potential or the contact metal work function.

cond-mat.mes-hall↗

arXiv2018

Enhanced Raman scattering of graphene using double resonance in silicon photonic crystal nanocavities

We demonstrate enhancements of Raman scattering from graphene on two-dimensional photonic crystals using double resonances, which originate from simultaneous enhancements by a localized guided mode and a cavity mode. By adjusting the photonic crystal cavity parameters, the double resonance can be tuned to the G' Raman scattering. Excitation wavelength dependence measurements show a large Raman peak enhancement when the excitation and emission wavelengths meet the double resonance condition. Furthermore, spatial imaging measurements are performed to confirm that the enhancement is localized at the cavity, and we find that the enhanced Raman intensity is 60 times larger compared to the on-substrate Raman signal. The observed cavity enhancement of Raman scattering opens up new possibilities for the development of graphene-based light sources for silicon photonics.

cond-mat.mes-hall↗