arXiv subjects

Takumi Nagasawa

Publications and source records attributed to Takumi Nagasawa.

3 recordsLinked to original sources

arXiv2026

Response of a Model Glass to Athermal Quasistatic Pinching

We numerically investigate the mechanical response of amorphous solids to localized force dipoles, referred to as pinching, using athermal quasistatic simulations of model glasses with varying degrees of stability. We employ a control parameter, the imposed extension, corresponding to the increase in rest length between the two pinched particles relative to their initial separation. Increasing this extension allows us to continuously tune the system from the elastic to the plastic regime. For small extensions, the response remains elastic. In this regime, the displacement field induced by pinching is well described by linear elasticity and exhibits a long-range power-law decay consistent with dipolar forcing. Averaged responses display anisotropic, quadrupolar-like patterns, with quantitative agreement between simulations and analytical predictions. This continuum description remains valid down to particle-scale distances. As the imposed extension increases, the response becomes plastic. Pinching can then trigger either localized or system-spanning rearrangements, depending on glass stability. Well-annealed glasses exhibit localized plastic events, whereas poorly annealed systems display delocalized cascades. We introduce a method to extract the principal axis of plastic deformation and analyze the associated displacement fields and plastic activity. Overall, our results demonstrate that pinching provides a minimal local probe of amorphous solids. The resulting response, governed by both glass stability and imposed extension, offers insight into the interplay between elasticity, elementary rearrangements, and the emergence of collective plasticity.

cond-mat.soft↗

arXiv2024

Infrared band strengths of dangling OH features in amorphous water at 20 K

Infrared (IR) spectra of vapor-deposited amorphous water at low temperatures show two weak peaks at around 3720 and 3696 cm-1 assigned to free-OH stretching modes of two- and three-coordinated water molecules (so-called dangling OH bonds), respectively, on the ice surface. A recent James Webb Space Telescope (JWST) observation first succeeded in detection of a potential dangling OH feature at 3664 cm-1 for ices in molecular clouds, highlighting the importance of dangling OH bonds in interstellar ice chemistry. A lack of band strengths of these features at low temperatures restricts the quantification of dangling OH bonds from IR spectra, hindering development of a molecular-level understanding of the surface structure and chemistry of ice. Using IR multiple-angle incidence resolution spectrometry, we quantified the band strengths of two- and three-coordinated dangling OH features in amorphous water at 20 K as being 4.6 plus-minus 1.6 times 10-18 and 9.1 plus-minus 1.0 times 10-18 cm molecule-1, respectively. These values are more than an order of magnitude lower than band strengths of bulk water molecules in ice and liquid water and are similar to those of H2O monomers confined in solid matrices. Adsorption of carbon monoxide with dangling OH bonds results in the appearance of a new broad dangling OH feature at 3680-3620 cm-1, with a band strength of 1.8 plus-minus 0.1 times 10-17 cm molecule-1. The band strengths of dangling OH features determined in this study advance our understanding of the surface structure of interstellar ice analogs and recent IR observations of the JWST.

astro-ph.GA↗

arXiv2022

Infrared multiple-angle incidence resolution spectrometry for vapor-deposited amorphous water

Infrared (IR) multiple-angle incidence resolution spectrometry (IR-MAIRS) is a recently developed spectroscopic technique that combines oblique incidence transmission measurements and chemometrics (multivariate analysis) to obtain both pure in-plane (IP) and out-of-plane (OP) vibration spectra for a thin sample. IR-MAIRS is established for analyzing the molecular orientation of organic thin films at atmospheric pressure, but it should also be powerful for the structural characterization of vapor-deposited thin samples prepared in a vacuum. The application of IR-MAIRS to vapor-deposited amorphous water is particularly interesting in the fields of physical and interstellar chemistry, because it is a representative model material for interstellar icy dust grains. We recently developed an experimental setup for in situ IR-MAIRS under low-temperature, ultra-high-vacuum conditions, which thus facilitates measurements of interstellar ice analogues such as vapor-deposited amorphous water. This review considers the theoretical framework of IR-MAIRS and our recent experimental results for vapor-deposited amorphous water. We present spectroscopic signatures for the perpendicular orientation of dangling OH bonds for three-coordinated water molecules at the surface of amorphous water at 90 K. The absolute absorption cross-section of the three-coordinated dangling OH bonds is quantitatively measured. As IR-MAIRS can essentially be conducted using only a Fourier-transform IR spectrometer and an angle-controllable linear polarizer, it is a useful, low-cost, and simple spectroscopic technique for studying laboratory analogues of interstellar ices including vapor-deposited amorphous water.

astro-ph.IM↗