arXiv subjects

Yuki Kobayashi

Publications and source records attributed to Yuki Kobayashi.

18 recordsLinked to original sources

arXiv2026

Enhancing Presence, Deepening Fan Intensity: How Presence in Immersive Video Shapes Psychological Closeness to Performers

Immersive video differs from conventional flat 2D video in that it is experienced as 180-degree stereoscopic video on a head-mounted display, thereby eliciting bodily and spatial subjective experience. Previous studies have shown that viewing and interpersonal distance affect Presence; however, it remains insufficiently understood how Presence differences are related to psychological closeness to content. In the present study, we examined whether differences in Presence could increase viewers' psychological closeness to performers within the content. This psychological closeness was operationally defined as fan intensity. Specifically, a live performance by a Japanese idol group was recorded as 180-degree immersive video, and a high-Presence condition (1.2 m) and a low-Presence condition (7.6 m) were established by manipulating filming distance. Twenty-four participants with different levels of prior involvement, comprising Avid fans and Casual fans, experienced both conditions in a counterbalanced within-participants design. Fan intensity was measured before and after the experience as perceived psychological overlap between the self and the performers. The results showed that, compared with the low-Presence condition, the high-Presence condition significantly increased all Presence-related measures except the Slater-Usoh-Steed questionnaire, with the largest condition differences observed for Possible Actions, Social Presence, and Observability. Moreover, a mixed analysis of variance on changes in fan intensity revealed a significant main effect of Presence condition, indicating that the high-Presence video produced a greater increase in fan intensity than the low-Presence video. These findings suggest that filming distance in immersive video is not merely a factor that determines angle of view or composition, but a design variable that can enhance Presence and deepen fan intensity.

cs.HC↗

arXiv2026

Nonresonant optomechanical control of structural phases

Optical tweezers demonstrate how light can exert forces to trap, repel, and manipulate microscopic particles without absorption. Recent theory has suggested that such forces can extend beyond particle manipulation to drive structural phase transitions in solids. Here we apply this optomechanical principle to tin selenide (SnSe), a material where proximity to several different structural phases gives rise to its high thermoelectric figure of merit and makes it a candidate for a switchable topological crystalline insulator. Whereas the force for standard optical tweezers arises from a gradient in the intensity of a light field, the optomechanical force is mediated by a gradient in the dielectric constant as a function of phonon coordinate. Unlike conventional methods that rely on resonant excitation and absorption through the imaginary part of the dielectric function, this approach operates dispersively through the real part and can be directly driven by Raman processes, enabling selective transitions with reduced energy cost and ultrafast response. Using time-domain Raman scattering, we show that above a critical mid-infrared field strength the $A_g$ Raman modes disappear abruptly without softening, signaling the formation of a new structural phase. This phase, distinct from those induced by heating or carrier excitation, exhibits large-amplitude and long-lived modulations in its optical response. Complementing this observation, we show also evidence for an equivalent DC-field-driven structural phase transformation to a higher symmetry phase, as observed by atom probe tomography. Our study demonstrates the concept of nonresonant optomechanical phase control and defines novel opportunities for synthesizing hidden structural phases with unique functional properties.

physics.optics↗

arXiv2026

Immersive XR That Moves People: How XR Advertising Transforms Comprehension, Empathy, and Behavioural Intention

Extended Reality (XR) affords an enhanced sense of bodily presence that supports experiential modes of comprehension and affective engagement which exceed the possibilities of conventional information delivery. Nevertheless, the psychological processes engendered by XR, and the manner in which these processes inform subsequent behavioural intentions, remain only partially delineated. The present study addresses this issue within an applied context by comparing non-immersive 2D viewing advertising with immersive XR experiential advertising. We examined whether XR strengthens internal responses to a product, specifically perceived comprehension and empathy, and whether these responses, in turn, influence the behavioural outcome of purchase intention. A repeated-measures two-way ANOVA demonstrated a significant main effect of advertising modality, with XR yielding higher ratings on all evaluative dimensions. Mediation analysis further indicated that the elevation in purchase intention was mediated by empathy, whereas no significant mediating effect was observed for comprehension within the scope of this study. These findings suggest that immersive XR experiences augment empathic engagement with virtual products, and that this enhanced empathy plays a pivotal role in shaping subsequent behavioural intentions.

cs.HC↗

arXiv2025

Different Rise Times of Atomic Br M$_{4,5}$ 3d$_{3/2,5/2}$ Core Level Absorptions during Br$_{2}$ C $^{1}Π_{u}$ $1_{u}$ State Dissociation via Extreme Ultraviolet Transient Absorption Spectroscopy

The reported ''dissociation times'' for the Br$_{2}$ C ($^{1}Π_{u}$ $1_{u}$) state by various measurement methods differ widely across the literature (30 to 340 fs). We consider this issue by investigating attosecond extreme ultraviolet (XUV) transient absorption spectroscopy at the Br M4,5 3d$_{3/2,5/2}$ edges (66 to 80 eV), tracking core-to-valence (3d to 4p) and core-to-Rydberg (3d to ns, np, n $\geq$ 5) transitions from the molecular to atomic limit. The progress of dissociation can be ascertained by the buildup of the atomic absorption in time. Notably, the measured rise times of the 3d$_{3/2,5/2}$ to 4p transitions depend on the probed core level final state, 38 $\pm$ 1 and 20 $\pm$ 5 fs for $^{2}$D$_{5/2}$ and $^{2}$D$_{3/2}$ at 64.31 and 65.34 eV, respectively. Simulations by the nuclear time-dependent Schrödinger equation reproduce the rise-time difference of the 3d to 4p transitions, and the theory suggests several important factors. One is the transition dipole moments of each probe transition have different molecular and atomic values for $^{2}$D$_{5/2}$ versus $^{2}$D$_{3/2}$ that depend on the bond length. The other is the merger of multiple molecular absorptions into the same atomic absorption, creating multiple timescales even for a single probe transition. Unfortunately, the core-to-Rydberg absorptions did not allow accurate atomic Br buildup times to be extracted due to spectral overlaps with ground state bleaching, otherwise an even more comprehensive picture of the role of the probe state transition would be possible. This work shows that the measured probe signals accurately contain the dissociative wavepacket dynamics but also reveal how the specific probe transition affects the apparent progress toward dissociation with bond length. Such potential probe-transition-dependent effects need to be considered when interpreting measured signals and their timescales.

physics.chem-ph↗

arXiv2025

Enhanced second-harmonic generation from WS$_2$/ReSe$_2$ heterostructure

Van der Waals stacking presents new opportunities for nonlinear optics with its remarkable tunability and scalability. However, the fundamental role of interlayer interactions in modifying the overall nonlinear optical susceptibilities remains elusive. In this letter, we report an anisotropic enhancement of second-harmonic generation (SHG) from a WS$_2$/ReSe$_2$ heterobilayer, where the individual composite layers possess distinctive crystal phases. We investigate polarization-resolved response and twist-angle dependence in SHG and reveal that band alignment alone is insufficient to explain the observed anisotropy in the modified SHG response. Spectral shifts in excitonic features highlight band renormalization, supporting the role of hybridization between the two layers. Furthermore, SHG enhancement is highly anisotropic and can even be suppressed in some orientations, suggesting possible intensity-borrowing mechanisms within the heterostructure. Our work demonstrates the ability to tune both the intensity and polarization dependence of nonlinear optical responses with van der Waals stacking of distinctive crystal phases.

cond-mat.mtrl-sci↗

arXiv2025

Determining the complex second-order optical susceptibility in macroscale van der Waals heterobilayers

We report on the experimental characterization of the second-order susceptibility in MoSe$_2$/WS$_2$ heterobilayers, including their hidden complex phases. To this end, we developed a heterodyne-detection scheme for second-harmonic generation and applied it to macroscale heterobilayer samples prepared using the gold-tape exfoliation method. The heterodyne scheme enabled us to distinguish the relative orientation of the crystal domains, and further, it allowed us to characterize the complex phases of the susceptibility relative to a reference quartz sample. By comparing the results from the monolayer regions and the heterobilayer region over several hundred microns of the sample area, we determined that the contribution of interlayer effects to second-harmonic generation is within the experimental uncertainty arising from the sample inhomogeneity. The results here provide fundamental quantitative information necessary for the precise design of nanophotonic systems based on stacking engineering.

cond-mat.mtrl-sci↗

arXiv2025

3D-Printed Enclosure Wire-Guided Liquid Microfilm for Versatile Spectroscopy

We present a 3D-printing-based design to produce wire-guided liquid microfilms that can be used for versatile spectroscopic applications. We demonstrate the ability of our instrument to provide optically useful liquid microfilms with highly tunable thicknesses over the range 25 - 180 $μ$m, with standard temporal thickness deviation less than 1.0% on the low end of the range of flow rates, and spatially homogeneous microfilms that remain stable over the course of ten hours. We then show the device's versatility through its use in Raman, fluorescence, and nonlinear spectroscopy. Our approach is highly reproducible as a unique advantage of a 3D-printed enclosure and limited other components. The 3D-printable file for the enclosure is included in the supplementary materials. This innovation in design shows the feasibility of applying 3D-printing to physical and chemical instrumentation for faster adoption of experimental techniques.

physics.chem-ph↗

arXiv2022

High-harmonic generation from artificially stacked 2D crystals

We report a coherent layer-by-layer high-order harmonic generation (HHG) build-up in artificially stacked transition metal dichalcogenides (TMDC) crystals in their various stacking configurations. In the experiments, millimeter-sized single crystalline monolayers are synthesized using the gold foil-exfoliation method, followed by artificially stacking on a transparent substrate. High-order harmonics up to the 19th order are generated by the interaction with an ultrafast mid-infrared (MIR) driving laser. We find that the generation is sensitive to the number of layers and their relative orientation. For AAAA stacking configuration, both odd- and even-orders exhibit a quadratic increase in intensity as a function of the number of layers, which is a signature of constructive interference of high-harmonic emission from successive layers. Particularly, we observe some deviations from this scaling at photon energies above the bandgap, which is explained by self-absorption effects. For AB and ABAB stacking, even-order harmonics remain below the detection level, consistent with the presence of inversion symmetry. Our study confirms the capability of producing non-perturbative high-order harmonics from stacked layered materials subjected to intense MIR fields without damaging samples. It has implications for optimizing solid-state HHG sources at the nano-scale and developing high-harmonics as an ultrafast probe of artificially stacked layered materials. Because the HHG process is a strong-field driven process, it has the potential to probe high-momentum and energy states in the bandstructure combined with atomic-scale sensitivity in real space, making it an attractive probe of novel material structures such as the Moiré pattern.

physics.optics↗

arXiv2022

Non-resonant Coherent Amplitude Transfer in Attosecond Four-Wave Mixing Spectroscopy

Attosecond four-wave mixing spectroscopy using an XUV pulse and two noncollinear near-infrared pulses is employed to measure Rydberg wavepacket dynamics resulting from extreme ultraviolet excitation of a 3s electron in atomic argon into a series of autoionizing 3s-1np Rydberg states around 29 eV. The emitted signals from individual Rydberg states exhibit oscillatory structure and persist well beyond the expected lifetimes of the emitting Rydberg states. These results reflect substantial contributions of longer-lived Rydberg states to the four wave mixing emission signals of each individually detected state. A wavepacket decomposition analysis reveals that coherent amplitude transfer occurs predominantly from photoexcited 3s-1(n+1)p states to the observed 3s-1np Rydberg states. The experimental observations are reproduced by time-dependent Schrödinger equation simulations using electronic structure and transition moment calculations. The theory highlights that coherent amplitude transfer is driven non-resonantly to the 3s-1np states by the near-infrared light through 3s-1(n+1)s and 3s-1(n-1)d dark states during the four-wave mixing process.

physics.atom-ph↗

arXiv2022

Floquet engineering of strongly-driven excitons in monolayer tungsten disulfide

Interactions of quantum materials with strong-laser fields can induce exotic nonequilibrium electronic states. Monolayer transition-metal dichalcogenides, a new class of direct-gap semiconductors with prominent quantum confinement, offer exceptional opportunities toward Floquet engineering of quasiparticle electron-hole states, or excitons. Strong-field driving has a potential to achieve enhanced control of electronic band structure, thus a possibility to open a new realm of exciton light-matter interactions. However, experimental implementation of strongly-driven excitons has so far remained out of reach. Here, we use mid-infrared laser pulses below the optical bandgap to excite monolayer tungsten disulfide up to a field strength of 0.3 V/nm, and demonstrate strong-field light dressing of excitons in the excess of a hundred millielectronvolt. Our high-sensitivity transient absorption spectroscopy further reveals formation of a virtual absorption feature below the 1s-exciton resonance, which is assigned to a light-dressed sideband from the dark 2p-exciton state. Quantum-mechanical simulations substantiate the experimental results and enable us to retrieve real-space movies of the exciton dynamics. This study advances our understanding of the exciton dynamics in the strong-field regime, and showcases the possibility of harnessing ultrafast, strong-field phenomena in device applications of two-dimensional materials.

cond-mat.mtrl-sci↗

arXiv2021

Theoretical analysis of the role of complex transition dipole phase in XUV transient-absorption probing of charge migration

We theoretically investigate the role of complex dipole phase in the attosecond probing of charge migration. The iodobromoacetylene ion (ICCBr$^+$) is considered as an example, in which one can probe charge migration by accessing both the iodine and bromine ends of the molecule with different spectral windows of an extreme-ultraviolet (XUV) pulse. The analytical expression for transient absorption shows that the site-specific information of charge migration is encoded in the complex phase of cross dipole products for XUV transitions between the I-$4d$ and Br-$3d$ spectral windows. Ab-initio quantum chemistry calculations on ICCBr$^+$ reveal that there is a constant $π$ phase difference between the I-$4d$ and Br-$3d$ transient-absorption spectral windows, irrespective of the fine-structure energy splittings. Transient absorption spectra are simulated with a multistate model including the complex dipole phase, and the results correctly reconstruct the charge-migration dynamics via the quantum beats in the two element spectral windows, exhibiting out-of-phase oscillations.

physics.chem-ph↗

arXiv2021

Probing Electron-Hole Coherence in Strongly-Driven Solids

High-harmonic generation (HHG) is a coherent optical process in which the incident photon energy is up-converted to the multiples of its initial energy. In solids, under the influence of a strong laser field, electron-hole (e-h) pairs are generated and subsequently driven to high energy and momentum within a fraction of the optical cycle. These dynamics encode the band structure, including non-trivial topological properties of the source material, through both intraband current and interband polarization, into the high harmonic spectrum. In the course of this process, dephasing between the driven electron and the hole can significantly reduce the HHG efficiency. Here, we exploit this feature and turn it into a measurement of e-h coherence in strongly driven solids. Utilizing a pre-pump pulse, we first photodope monolayer molybdenum disulfide and then examine the HHG induced by an intense infrared pulse. We observe clear suppression of the HH intensity, which becomes more pronounced with increasing order. Based on quantum simulations, we attribute this monotonic order dependence as a signature of ultrafast electron-hole dephasing, which leads to an exponential decay of the inter-band polarization, proportional to the sub-cycle excursion time of the e-h pair. Our results demonstrate the importance of many-body effects, such as density-dependent decoherence in HHG and provide a novel platform to probe electron-hole coherence in strongly driven systems.

physics.optics↗

arXiv2020

Attosecond XUV probing of vibronic quantum superpositions in Br$_2^+$

Ultrafast laser excitation can create coherent superpositions of electronic states in molecules and trigger ultrafast flow of electron density on few- to sub-femtosecond time scales. While recent attosecond experiments have addressed real-time observation of these primary photochemical processes, the underlying roles of simultaneous nuclear motions and how they modify and disturb the valence electronic motion remain uncertain. Here, we investigate coherent electronic-vibrational dynamics induced among multiple vibronic levels of ionic bromine (Br$_2^+$), including both spin-orbit and valence electronic superpositions, using attosecond transient absorption spectroscopy. Decay, revival, and apparent frequency shifts of electronic coherences are measured via characteristic quantum beats on the Br-$3d$ core-level absorption signals. Quantum-mechanical simulations attribute the observed electronic decoherence to broadened phase distributions of nuclear wave packets on anharmonic potentials. Molecular vibronic structure is further revealed to be imprinted as discrete progressions in electronic beat frequencies. These results provide a future basis to interpret complex charge-migration dynamics in polyatomic systems.

physics.chem-ph↗

arXiv2020

Revealing electronic state-switching at conical intersections in alkyl iodides by ultrafast XUV transient absorption spectroscopy

Conical intersections between electronic states often dictate the chemistry of photoexcited molecules. Recently developed sources of ultrashort extreme ultraviolet (XUV) pulses tuned to element-specific transitions in molecules allow for the unambiguous detection of electronic state-switching at a conical intersection. Here, the fragmentation of photoexcited iso-propyl iodide and tert-butyl iodide molecules (i-C$_{3}$H$_{7}$I and t-C$_{4}$H$_{9}$I) through a conical intersection between $^{3}$Q$_{0}$/$^{1}$Q$_{1}$ spin-orbit states is revealed by ultrafast XUV transient absorption measuring iodine 4d core-to-valence transitions. The electronic state-sensitivity of the technique allows for a complete mapping of molecular dissociation from photoexcitation to photoproducts. In both molecules, the sub-100 fs transfer of a photoexcited wave packet from the $^{3}$Q$_{0}$ state into the $^{1}$Q$_{1}$ state at the conical intersection is captured. The results show how differences in the electronic state-switching of the wave packet in i-C$_{3}$H$_{7}$I and t-C$_{4}$H$_{9}$I directly lead to differences in the photoproduct branching ratio of the two systems.

physics.chem-ph↗

arXiv2020

Coherent electronic-vibrational dynamics in deuterium bromide probed via attosecond transient absorption spectroscopy

Ultrafast laser excitation can trigger multiplex coherent dynamics in molecules. Here, we report attosecond transient absorption experiments addressing simultaneous probing of electronic and vibrational dynamics in a prototype molecule, deuterium bromide (DBr), following its strong-field ionization. Electronic and vibrational coherences in the ionic X$^2Π_{3/2}$ and X$^2Π_{1/2}$ states are characterized in the Br-$3d$ core-level absorption spectra via quantum beats with 12.6-fs and 19.9-fs periodicities, respectively. Polarization scans reveal that the phase of the electronic quantum beats depends on the probe direction, experimentally showing that the coherent electronic motion corresponds to the oscillation of the hole density along the ionization-field direction. The vibrational quantum beats are found to maintain a relatively constant amplitude, whereas the electronic quantum beats exhibit a partial decrease in time. Quantum wave-packet simulations show that the decoherence effect from the vibrational motion is insignificant because of the parallel relation between the X$^2Π_{3/2}$ and X$^2Π_{1/2}$ potentials. A comparison between the DBr and HBr results suggests that rotation motion is responsible for the decoherence since it leads to initial alignment prepared by the strong-field ionization.

physics.chem-ph↗

arXiv2020

Attosecond spectroscopy reveals alignment dependent core-hole dynamics in the ICl molecule

The removal of electrons located in the core shells of molecules creates transient states that live between a few femtoseconds to attoseconds. Owing to these short lifetimes, time-resolved studies of these states are challenging and complex molecular dynamics driven solely by electronic correlation are difficult to observe. Here, few-femtosecond core-excited state lifetimes of iodine monochloride are obtained by attosecond transient absorption on iodine 4d-16p transitions around 55 eV. Core-level ligand field splitting allows direct access of excited states aligned along and perpendicular to the ICl molecular axis. Lifetimes of 3.5 fs and 4.3 fs are obtained for core-hole states parallel to the bond and 6.5 fs and 6.9 fs for perpendicular states, while nuclear motion is essentially frozen on this timescale. Theory shows that the dramatic decrease of lifetime for core-vacancies parallel to the covalent bond is a manifestation of non-local interactions with the neighboring Cl atom of ICl.

physics.chem-ph↗

arXiv2019

Gas-phase structural isomer identification by Coulomb explosion of aligned molecules

The gas-phase structures of four difluoroiodobenzene and two dihydroxybromobenzene isomers were identified by correlating the emission angles of atomic fragment ions created following femtosecond laser-induced Coulomb explosion. The structural determinations were facilitated by confining the most polarizable axis of each molecule to the detection plane prior to the Coulomb explosion event using one-dimensional laser-induced adiabatic alignment. For a molecular target consisting of two difluoroiodobenzene isomers, each constituent structure could additionally be singled out and distinguished.

physics.chem-ph↗

arXiv2006

Generalized Area Law under Multi-parameter Rotating Black Hole Spacetime

We study the statistical mechanics for quantum scalar fields under the multi-parameter rotating black hole spacetime in arbitrary D dimensions. The method of analysis is general in the sense that the metric does not depend on the explicit black hole solutions. The generalized Stefan-Boltzmann's law for the scalar field is derived by considering the allowed energy region properly. Then the generalized area law for the scalar field entropy is derived by introducing the invariant regularization parameter in the Rindler spacetime. The derived area law is applied to Kerr-AdS black holes in four and five dimensions. Thermodynamic implication is also discussed.

gr-qc↗