arXiv subjects

Yuki Yoshikawa

Publications and source records attributed to Yuki Yoshikawa.

4 recordsLinked to original sources

arXiv2026

Development and Characterization of Low-Scattering Vanadium Nanoparticle Targets for Short-Range Interaction Searches

We developed high-purity vanadium-based nanoparticle targets for neutron scattering experiments aimed at exploring gravity-like short-range new interactions in the submicron regime. Vanadium and V-Ni nanoparticles were fabricated using top-down and bottom-up methods and quantitatively characterized by SEM-EDS, ICP-AES, NDIR and SAXS. Through the performance tests, an RF thermal plasma method was found to be the best from viewpoints of the reproducibility, dispersion of the radius, and contamination of metallic elements. The oxygen incorporation during fabrication was quantified, and its impact on the effective coherent scattering length was evaluated, leading to a minimum average coherent scattering length of $\mathrm{0.719(23)\,fm}$, comparable to that of natural vanadium. These results demonstrate that vanadium-based nanoparticle targets with controlled composition and nanostructure can be systematically designed and fabricated to suppress nuclear scattering backgrounds, thereby enabling experimentally viable coherent neutron scattering measurements for short-range interaction searches.

physics.ins-det↗

arXiv2021

Temperature Dependence of Polymer Network Diffusion

The swelling dynamics of polymer gels are characterized by the (collective) diffusion coefficient $D$ of the polymer network. Here, we measure the temperature dependence of $D$ of polymer gels with controlled homogeneous network structures using dynamic light scattering. An evaluation of the diffusion coefficient at the gelation point $D_{\mathrm{gel}}$ and the increase therein as the gelation proceeds $ΔD\equiv D-D_{\mathrm{gel}}$ indicates that $ΔD$ is a linear function of the absolute temperature with a significantly large negative constant term. This feature is formally identical to the recently discovered "negative energy elasticity" [Y. Yoshikawa et al., Phys. Rev. X 11, 011045 (2021) (arXiv:1912.13191)], demonstrating a nontrivial similarity between the statics and dynamics of polymer networks.

cond-mat.soft↗

arXiv2021

Linear elasticity of polymer gels in terms of negative energy elasticity

We recently found that the energy contribution to the linear elasticity of polymer gels in the as-prepared state can be a significant negative value; the shear modulus is not proportional to the absolute temperature [Y. Yoshikawa et al., Phys. Rev. X 11, 011045 (2021) (arXiv:1912.13191)]. Our finding challenges the conventional notion that the polymer-gel elasticity is mainly determined by the entropy contribution. Existing molecular models of classical rubber elasticity theories, including the affine, phantom, and junction affine network models, cannot be used to estimate the structural parameters of polymer gels. In this focus review, we summarize the experimental studies on the linear elasticity of polymer gels in the as-prepared state using tetra-arm poly(ethylene glycol) (PEG) hydrogels with a homogenous polymer network. We also provide a unified formula for the linear elasticity of polymer gels with various network topologies and densities. Using the unified formula, we reconcile the past experimental results that seemed to be inconsistent with each other. Finally, we mention that there are still fundamental unresolved problems involving the linear elasticity of polymer gels.

cond-mat.soft↗

arXiv2021

Negative energy elasticity in a rubberlike gel

Rubber elasticity is the archetype of the entropic force emerging from the second law of thermodynamics; numerous experimental and theoretical studies on natural and synthetic rubbers have shown that the elasticity originates mostly from entropy change with deformation. Similarly, in polymer gels containing a large amount of solvent, it has also been postulated that the shear modulus (the modulus of rigidity) $G$, which is a kind of modulus of elasticity, is approximately equivalent to the entropy contribution $G_S$, but this has yet to be verified experimentally. In this study, we measure the temperature dependence of the shear modulus $G$ in a rubberlike (hyperelastic) polymer gel whose polymer volume fraction is at most 0.1. As a result, we find that the energy contribution $G_E=G-G_S$ can be a significant negative value, reaching up to double the shear modulus $G$ (i.e., $\left|G_E\right| \simeq 2G$), although the shear modulus of stable materials is generally bound to be positive. We further argue that the energy contribution $G_E$ is governed by a vanishing temperature that is a universal function of the normalized polymer concentration, and $G_E$ vanishes when the solvent is removed. Our findings highlight the essential difference between rubber elasticity and gel elasticity (which were previously thought to be the same) and push the established field of gel elasticity into a new direction.

cond-mat.soft↗