arXiv subjects

Toshiki Sugimoto

Publications and source records attributed to Toshiki Sugimoto.

9 recordsLinked to original sources

arXiv2026

Tip-Enhanced Vibrational Ladder Climbing in Surface Molecular System

Achieving high-lying vibrational states is essential for actively controlling molecular reactions. We demonstrate vibrational ladder climbing of CO adsorbed on Pt(111) within the plasmonic tip-substrate nanogap formed in a scanning tunneling microscope, detected via tip-enhanced sum-frequency generation (TE-SFG). As the infrared pulse energy increases, hot-band peaks appear sequentially up to the 3-4 transition, indicating the stepwise population of higher vibrational states. Numerical analysis using the optical Bloch equations captures the observed energy dependence of these features. These results demonstrate the capability of TE-SFG to probe vibrational ladder climbing in surface molecular systems and suggest a promising route toward accessing high-lying vibrational states and controlling vibrational excitation at the nanoscale.

physics.optics↗

arXiv2026

Plasmonic- and Electronic-Enhancement-Free Coherent Raman Detection of Ångström-Scale Molecular Layers at Metal Interfaces

Coherent Raman scattering provides highly sensitive vibrational analysis through nonlinear light-matter interactions. However, its application to metal interfaces has remained challenging because the intrinsically large non-resonant background (NRB) of metals overwhelms weak interfacial molecular vibrational signals, making direct Raman detection without plasmonic or electronic enhancement highly challenging. Here, we report a time-frequency hybrid coherent Raman spectroscopy approach that overcomes this limitation and enables sensitive detection of ångström-thick molecular systems even on atomically flat metal surfaces. Our method employs a time-frequency engineered detection scheme that combines femtosecond pump and Stokes pulses with a time-delayed, asymmetrically shaped picosecond probe pulse. By exploiting instantaneous temporal response of the metal NRB, this pulse configuration effectively filters out the dominant metal NRB in the time domain while retaining a controlled residual NRB that acts as an internal local oscillator, enabling strong interferometric amplification of weak interfacial vibrational signatures. This all-optical coherent enhancement strategy establishes a new route for direct, non-invasive Raman detection of interfacial molecular systems across a wide range of surfaces without requiring structure- and material-specific plasmonic and electronic enhancement mechanisms.

physics.optics↗

arXiv2026

H$_2$ Ortho-Para Spin Conversion on Inhomogeneous Grain Surfaces. II. impact of the rotational energy difference between adsorbed ortho-H$_2$ and para-H$_2$ and implication to deuterium fractionation chemistry

We investigate how the H$_2$ ortho-to-para ratio (OPR) and dueterium fractionation in star-forming regions are affected by nuclear spin conversion (NSC) on dust grains. Particular focus is placed on the rotational energy difference between ortho-H$_2$ (o-H$_2$) and para-H$_2$ (p-H$_2$) on grain surfaces. While the ground state of o-H$_2$ has a higher rotational energy than that of p-H$_2$ by 170.5 K in the gas phase, this energy difference is expected to become smaller on solid surfaces, where interactions between the surface and adsorbed H$_2$ molecules affect their rotational motion. A previous study by Furuya et al. (2019) developed a rigorous formulation of the rate for the temporal variation of the H$_2$ OPR via the NSC on grains, assuming that adsorbed o-H$_2$ has higher rotational energy than adsorbed p-H$_2$ by 170.5 K, as in the gas phase. In this work, we relax the assumption and re-evaluate the rate, varying the rotational energy difference between their ground states. The re-evaluated rate is incorporated into a gas-ice astrochemical model to study the evolution of the H$_2$ OPR and the deuterium fractionation in prestellar cores and the outer, cold regions of protostellar envelopes. The inclusion of the NSC on grains reduces the timescale of the H2 OPR evolution and thus the deuterium fractionation, at densities of >10$^4$ cm$^{-3}$ and temperatures of <14-16 K (depending on the rotational energy difference), when the ionization rate of H$_2$ is 10$^{-17}$ s$^{-1}$.

astro-ph.GA↗

arXiv2025

Phase-sensitive tip-enhanced sum frequency generation spectroscopy using temporally asymmetric pulse for detecting weak vibrational signals

Vibrational sum frequency generation (SFG) spectroscopy is a powerful technique for investigating molecular structures, orientations, and dynamics at surfaces. However, its spatial resolution is fundamentally restricted to the micrometer scale by the optical diffraction limit. Tip-enhanced SFG (TE-SFG) using a scanning tunneling microscope has been developed to overcome this limitation. The acquired spectra exhibit characteristic dips originating from vibrational responses located within the strong broadband non-resonant background (NRB), which distorts and obscures the molecular signals. By making the second pulse temporally asymmetric and introducing a controlled delay between the first and second laser pulses, the NRB was effectively suppressed, which in turn amplified the vibrational response through interference and facilitated the detection of weak vibrational signals. This interference also made the technique phase-sensitive, enabling the determination of absolute molecular orientations. Furthermore, forward- and backward-scattered signals were simultaneously detected, conclusively confirming that the observed signals originated from tip enhancement rather than far-field contributions. Finally, the signal enhancement factor in TE-SFG was estimated to be $6.3\times 10^6-1.3\times 10^7$, based on the experimental data. This phase-sensitive TE-SFG technique overcomes the optical diffraction limit and enables the investigation of molecular vibrations at surfaces with unprecedented detail.

physics.optics↗

arXiv2025

Giant near-field nonlinear electrophotonic effects in an angstrom-scale plasmonic junction

Plasmons facilitate a strong confinement and enhancement of near-field light, offering exciting opportunities to enhance nonlinear optical responses at the nanoscale. However, despite significant advancements, the electrically tunable range of the nonlinear optical responses at nanometer-scale plasmonic structures remains limited to a few percents per volt. Here, we transcend the limitation of the nanometer regime by expanding the concept of electrophotonics into angstrom-scale platform, enabling high-performance modulation of near-field nonlinear optical responses inaccessible in prior architectures. We demonstrate ~2000% enhancement in second-harmonic generation (SHG) within 1 V of voltage application by utilizing an angstrom-scale plasmonic gap between a metallic tip and a flat metal substrate in a scanning tunneling microscope. Extending this near-field SHG scheme to sum-frequency generation that is accompanied by large frequency upconversion, we also found that such giant electrical modulation of plasmon-enhanced nonlinear optical phenomena is effective over mid-infrared to visible broad wavelength range. Our results and concepts lay the foundation for developing near-field-based angstrom-scale nonlinear electrophotonics with significant modulation depth at low driving voltage.

physics.optics↗

arXiv2025

Diffraction-Unlimited Tip-Enhanced Sum-Frequency Vibrational Nanoscopy

Sum-frequency generation (SFG) is a powerful second-order nonlinear spectroscopic technique that provides detailed insights into molecular structures and absolute orientations at surfaces and interfaces. However, conventional SFG based on far-field schemes suffers from the diffraction limit of light, which inherently averages spectroscopic information over micrometer-scale regions and obscures nanoscale structural inhomogeneity. Here, we overcome this fundamental limitation by leveraging a highly confined optical near field within a tip-substrate nanogap of a scanning tunneling microscope (STM), pushing the spatial resolution of SFG down to ~10 nm, a nearly two-orders-of-magnitude improvement over conventional far-field SFG. By capturing tip-enhanced SFG (TE-SFG) spectra concurrently with STM scanning, we demonstrate the capability to resolve nanoscale variation in molecular adsorption structures across distinct interfacial domains. To rigorously interpret the observed TE-SFG spectra, we newly developed a comprehensive theoretical framework for the TE-SFG process and confirm via numerical simulations that the TE-SFG response under our current experimental conditions is dominantly governed by the dipole-field interactions, with negligible contributions from higher-order multipole effects. The dominance of the dipole mechanism ensures that the observed TE-SFG spectra faithfully reflect not only nanoscale interfacial structural features but also absolute up/down molecular orientations. This study presents the first experimental realization of diffraction-unlimited second-order nonlinear vibrational SFG nanoscopy, opening a new avenue for nanoscale domain-specific investigation of molecular structures and dynamics within inhomogeneous interfacial molecular systems beyond the conventional far-field SFG and STM imaging.

physics.optics↗

arXiv2025

Dramatic Enhancement of Supercontinuum Generation in H$_2$O by Non-Harmonic Two-Color Excitation

We demonstrate a dramatic enhancement of supercontinuum generation (SCG) in H$_2$O driven by non-harmonic two-color laser fields, where pump and seed frequencies are not integer multiples. This scheme yields a broadband SC spectrum enhanced by approximately three orders of magnitude over the single-color case. Systematic experiments and theoretical analysis, including isotope effects, show that the enhancement arises from soliton compression with resonant dispersive wave (RDW) emission, phase- and group-velocity-matched four-wave mixing (FWM), and cross-phase modulation (XPM), offering a versatile route to stronger SCG and noise suppression in broadband spectroscopy in H$_2$O, an emerging topic in attosecond and surface physics.

physics.optics↗

arXiv2025

Picocavity-Enhanced Raman Spectroscopy of Physisorbed H$_2$ and D$_2$ Molecules

We report on tip-enhanced Raman spectroscopy of H2 and D2 molecules physisorbed within a plasmonic picocavity at 10 K. The intense Raman peaks resulting from the rotational and vibrational transitions are observed at subnanometer gap distances of the junction formed by an Ag tip and an Ag(111) surface, where a picocavity-enhanced field plays a crucial role. A significant redshift of the H-H stretch frequency is observed as the gap distance decreases, while the D-D stretch frequency is unaffected. Density functional theory, path-integral molecular dynamics, and quantum anharmonic vibrational energy calculations suggest that this unexpected isotope effect is explained by a different molecular density between H2 and D2 on the surface.

physics.optics↗

arXiv2024

Tip-Enhanced Sum Frequency Generation for Molecular Vibrational Nanospectroscopy

Vibrational sum frequency generation (SFG) is a nonlinear spectroscopic technique widely used to study the molecular structure and dynamics of surface systems. However, the spatial resolution achieved by far-field observations is constrained by the diffraction limit, obscuring molecular details in inhomogeneous structures smaller than the wavelength of light. To overcome this limitation, we developed a system for tip-enhanced SFG (TE-SFG) spectroscopy based on a scanning tunneling microscope. We successfully detected vibrational TE-SFG signals from adsorbed molecules on a gold substrate under ambient conditions. The phase analysis of interferometric SFG spectra provided information on molecular orientation. Furthermore, the observed TE-SFG signal was confirmed to originate from a highly localized region within a gap between the tip apex and the sample substrate. This method offers a novel platform for nonlinear optical nanospectroscopy, paving the way for the investigation of surface molecular systems beyond the diffraction limit.

physics.optics↗