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S. Maruyama

Publications and source records attributed to S. Maruyama.

At least 19 recordsLinked to original sources

Robust chirality memory in carbon nanotubes growing under modulated and evolving environments

Controlling the chirality and yield of carbon nanotubes is essential for their diverse applications from macroscopic composites to nanoelectronics. Floating-catalyst chemical vapor deposition is widely employed as a scalable synthesis route, where catalysts inevitably traverse spatially varying environments. However, prevailing interpretations of nanotube growth largely rely on ensemble monitoring or static, post-growth snapshots. Here, we combine digital isotope labeling with programmed temperature modulation to reconstruct the dynamic growth histories of supported individual nanotubes. Growth rates exhibit hysteresis and extraordinary sensitivity to temperature changes, indicating irreversible catalyst coarsening; nevertheless, the nanotube chirality remains robustly preserved across lengths exceeding 300 um. This sharp contrast between kinetic adaptability and structural memory in nanotube growth indicates that chirality control can be established at the nucleation stage, while allowing independent optimization of subsequent elongation. Our findings further call for a re-examination of static interpretations of diameter-determination mechanisms derived from post-growth snapshots.

cond-mat.mtrl-sci

Generation of giga-electron-volt proton beams by micronozzle acceleration

Our proposed ion acceleration scheme, micronozzle acceleration (MNA), generates proton beams with extremely high kinetic energies on the giga-electron-volt (GeV) order. The underlying physics and performance of MNA are studied with two-dimensional particle-in-cell simulations. In MNA targets, a micron-sized hydrogen rod is embedded inside a hollow micronozzle. Subsequent illumination of the target along the symmetric axis by an ultraintense ultrashort laser pulse forms a strong electrostatic field with a long lifetime and an extensive space around the downstream tail of the nozzle. The electric field significantly amplifies the kinetic energies of the accelerated protons, and > GeV protons are generated at an applied laser intensity of 10^22 W/cm^2 .

physics.plasm-ph

Catalyst-mediated etching of carbon nanotubes exhibiting electronic-structure insensitivity and reciprocal kinetics with growth

The selective etching of carbon nanotubes has been widely explored as a post-synthetic route for enriching semiconducting species. As nanoelectronic applications increasingly demand pure semiconducting nanotubes for use in field-effect transistors and other optoelectronic devices, understanding the mechanistic basis of selective removal becomes critical. While etching selectivity is often attributed to electronic structure effects on tube walls, its relevance in the presence of catalyst nanoparticles remains unclear. Here, we directly quantify the catalyst-mediated etching and growth rates of individual single-walled carbon nanotubes using elaborate isotope labeling methods. Surprisingly, in water vapor and methanol environments, catalytic etching proceeds with negligible dependence on tube electronic type, in sharp contrast to non-catalytic oxidation pathways. In-situ Raman analysis upon heating on nanotube ensembles also confirms metallicity-insensitive etching under catalytic conditions, whereas sidewall oxidation without catalysts exhibits pronounced selectivity. Our growth kinetic model, which precisely describes the kinetics of catalytic etching process, motivates kinetic Monte Carlo simulations of nanotube edge dynamics, revealing the reciprocal nature of edge configuration during growth and etching. These findings highlight a fundamental mechanistic distinction between catalytic and non-catalytic reactivity and thus propose that catalytic etching may serve as a diagnostic mirror of growth behavior when using pre-sorted carbon nanotube samples.

cond-mat.mtrl-sci

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

Intertube excitonic coupling in nanotube van der Waals heterostructures

Excitons dominate the optics of atomically-thin transition metal dichalcogenides and 2D van der Waals heterostructures. Interlayer 2D excitons, with an electron and a hole residing in different layers, form rapidly in heterostructures either via direct charge transfer or via Coulomb interactions that exchange energy between layers. Here, we report prominent intertube excitonic effects in quasi-1D van der Waals heterostructures consisting of C/BN/MoS$_2$ core/shell/skin nanotubes. Remarkably, under pulsed infrared excitation of excitons in the semiconducting CNTs we observed a rapid (sub-picosecond) excitonic response in the visible range from the MoS$_2$ skin, which we attribute to intertube biexcitons mediated by dipole-dipole Coulomb interactions in the coherent regime. On longer ($>100$ps) timescales hole transfer from the CNT core to the MoS$_2$ skin further modified the MoS$_2$'s absorption. Our direct demonstration of intertube excitonic interactions and charge transfer in 1D van der Waals heterostructures suggests future applications in infrared and visible optoelectronics using these radial heterojunctions.

cond-mat.mes-hall

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

Laser-beam patterned topological insulating states on thin semiconducting MoS2

Identifying the two-dimensional (2D) topological insulating (TI) state in new materials and its control are crucial aspects towards the development of voltage-controlled spintronic devices with low power dissipation. Members of the 2D transition metal dichalcogenides (TMDCs) have been recently predicted and experimentally reported as a new class of 2D TI materials, but in most cases edge conduction seems fragile and limited to the monolayer phase fabricated on specified substrates. Here, we realize the controlled patterning of the 1T'-phase embedded into the 2H-phase of thin semiconducting molybdenum-disulfide (MoS2) by laser beam irradiation. Integer fractions of the quantum of resistance, the dependence on laser-irradiation conditions, magnetic field, and temperature, as well as the bulk gap observation by scanning tunneling spectroscopy and theoretical calculations indicate the presence of the quantum spin Hall phase in our patterned 1T' phases.

cond-mat.mes-hall

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

Electric-field Induced Reversible Switching of the Magnetic Easy-axis in Co/BiFeO3/SrRuO3/SrTiO3 Heterostructures

Electric-field (E-field) control of magnetism enabled by multiferroics has the potential to revolutionize the landscape of present memory devices plagued with high energy dissipation. To date, this E-field controlled multiferroic scheme at room temperature has only been demonstrated using BiFeO3 (BFO) films grown on DyScO3 (refs 1 and 2), a unique and expensive substrate, which gives rise to a particular ferroelectric domain pattern in BFO. Here, we demonstrate reversible E-field-induced switching of the magnetic state of the Co layer in Co/BFO (001) thin film heterostructures fabricated on SrTiO3 substrates. The angular dependence of the coercivity and the remanent magnetization of the Co layer indicates that its easy axis reversibly switches by 45° back and forth between the (100) and the (110) crystallographic directions of SrTiO3 as a result of alternating application of positive and negative voltage pulses on BFO. The coercivity of the Co layer exhibits a hysteretic behavior between two states as a function of voltage. To explain the observation, we have also measured the exact canting angle of the antiferromagnetic G-type domain in BFO films for the first time using neutron diffraction. These results suggest a pathway to integrating BFO-based devices on Si wafers for implementing low power consumption and non-volatile magnetoelectronic devices.

cond-mat.mtrl-sci

Enhancement of carbon nanotube photoluminescence by photonic crystal nanocavities

Photonic crystal nanocavities are used to enhance photoluminescence from single-walled carbon nanotubes. Micelle-encapsulated nanotubes are deposited on nanocavities within Si photonic crystal slabs and confocal microscopy is used to characterize the devices. Photoluminescence spectra and images reveal nanotube emission coupled to nanocavity modes. The cavity modes can be tuned throughout the emission wavelengths of carbon nanotubes, demonstrating the ability to enhance photoluminescence from a variety of chiralities.

cond-mat.mes-hall

Gate-induced blueshift and quenching of photoluminescence in suspended single-walled carbon nanotubes

Gate-voltage effects on photoluminescence spectra of suspended single-walled carbon nanotubes are investigated. Photoluminescence microscopy and excitation spectroscopy are used to identify individual nanotubes and to determine their chiralities. Under an application of gate voltage, we observe slight blueshifts in the emission energy and strong quenching of photoluminescence. The blueshifts are similar for different chiralities investigated, suggesting extrinsic mechanisms. In addition, we find that the photoluminescence intensity quenches exponentially with gate voltage.

cond-mat.mes-hall

Exciton diffusion in air-suspended single-walled carbon nanotubes

Direct measurements of the diffusion length of excitons in air-suspended single-walled carbon nanotubes are reported. Photoluminescence microscopy is used to identify individual nanotubes and to determine their lengths and chiral indices. Exciton diffusion length is obtained by comparing the dependence of photoluminescence intensity on the nanotube length to numerical solutions of diffusion equations. We find that the diffusion length in these clean, as-grown nanotubes is significantly longer than those reported for micelle-encapsulated nanotubes.

cond-mat.mes-hall

Acetylene-Accelerated Alcohol Catalytic CVD Growth of Vertically Aligned Single-Walled Carbon Nanotubes

Addition of only 1% of acetylene into ethanol was found to enhance the growth rate of singlewalled carbon nanotubes (SWNTs) by up to ten times. Since acetylene is a byproduct of the thermal decomposition of ethanol, this suggests an alternative fast reaction pathway to the formation of SWNTs from ethanol via byproducts of decomposition. This accelerated growth, however, only occurred in the presence of ethanol, whereas pure acetylene at the same partial pressure resulted in negligible growth and quickly deactivated the catalyst. The dormant catalyst could be revived by reintroduction of ethanol, indicating that catalyst deactivation is divided into reversible and irreversible stages.

cond-mat.mtrl-sci

Linear plasmon dispersion in single-wall carbon nanotubes and the collective excitation spectrum of graphene

We have measured a strictly linear pi-plasmon dispersion along the axis of individualized single wall carbon nanotubes, which is completely different from plasmon dispersions of graphite or bundled single wall carbon nanotubes. Comparative ab initio studies on graphene based systems allow us to reproduce the different dispersions. This suggests that individualized nanotubes provide viable experimental access to collective electronic excitations of graphene, and it validates the use of graphene to understand electronic excitations of carbon nanotubes. In particular, the calculations reveal that local field effects (LFE) cause a mixing of electronic transitions, including the 'Dirac cone', resulting in the observed linear dispersion.

cond-mat.str-el

Millimeter-Thick Single-Walled Carbon Nanotube Forests: Hidden Role of Catalyst Support

A parametric study of so-called "super growth" of single-walled carbon nanotubes(SWNTs) was done by using combinatorial libraries of iron/aluminum oxide catalysts. Millimeter-thick forests of nanotubes grew within 10 min, and those grown by using catalysts with a thin Fe layer (about 0.5 nm) were SWNTs. Although nanotube forests grew under a wide range of reaction conditions such as gas composition and temperature, the window for SWNT was narrow. Fe catalysts rapidly grew nanotubes only when supported on aluminum oxide. Aluminum oxide, which is a well-known catalyst in hydrocarbon reforming, plays an essential role in enhancing the nanotube growth rates.

cond-mat.mtrl-sci

Meissner effect in honeycomb arrays of multi-walled carbon nanotubes

We report Meissner effect for type-II superconductors with a maximum Tc of 19 K, which is the highest value among those in new-carbon related superconductors, found in the honeycomb arrays of multi-walled CNTs (MWNTs). Drastic reduction of ferromagnetic catalyst and efficient growth of MWNTs by deoxidization of catalyst make the finding possible. The weak magnetic anisotropy, superconductive coherence length (- 7 nm), and disappearance of the Meissner effect after dissolving array structure indicate that the graphite structure of an MWNT and those intertube coupling in the honeycomb array are dominant factors for the mechanism.

cond-mat.supr-con

Magnetic Brightening of Carbon Nanotube Photoluminescence through Symmetry Breaking

Often a modification of microscopic symmetry in a system can result in a dramatic change in its macroscopic properties. Here we report that symmetry breaking by a tube-threading magnetic field can drastically increase the photoluminescence quantum yield of semiconducting single-walled carbon nanotubes, by as much as a factor of six, at low temperatures. To explain this striking connection between seemingly unrelated properties, we have developed a comprehensive theoretical model based on magnetic-field-dependent one-dimensional exciton band structure and the interplay of strong Coulomb interactions and the Aharonov-Bohm effect. This conclusively explains our data as the first experimental observation of dark excitons 5-10 meV below the bright excitons in single-walled carbon nanotubes. We predict that this quantum yield increase can be made much larger in disorder-free samples.

cond-mat.mes-hall

Anisotropic Decay Dynamics of Photoexcited Aligned Carbon Nanotube Bundles

We have performed polarization-dependent ultrafast pump-probe spectroscopy of a film of aligned single-walled carbon nanotube bundles. By taking into account imperfect nanotube alignment as well as anisotropic absorption cross sections, we quantitatively determined distinctly different photo-bleaching dynamics for polarizations parallel and perpendicular to the tube axis. For perpendicular polarization, we observe a slow (1.0-1.5 ps) relaxation process, previously unobserved in randomly-oriented nanotube bundles. We attribute this slower dynamics to the excitation and relaxation of surface plasmons in the radial direction of the nanotube bundles.

cond-mat.mes-hall