SearcharxivSearch

arXiv subjects

Sho Kawakami

Publications and source records attributed to Sho Kawakami.

5 recordsLinked to original sources

Translation of a spherical viscous drop driven by localized forcing in Stokes flow

Localized forcing in the fluid inside or outside a viscous drop can drive drop translation. Using the Lorentz reciprocal theorem, we derive an integral expression for the translational velocity of a spherical Newtonian drop subject to localized force and source distributions in either fluid and to interfacial traction. For a clean drop, we obtain explicit responses to Stokeslets, force dipoles, rotlets, general second force moments, and source dipoles as functions of position, orientation, and viscosity ratio. Interior forcing obeys a finite selection rule: only force moments through second order and the first source moment contribute directly to translation. Exterior forcing can couple to multipoles of all orders and produces distance-dependent responses. Although different enclosed singularities can produce the same drop velocity, resolving their exterior flows in drop-centered spherical Stokes modes provides additional constraints on the underlying forcing. We also distinguish regularized force distributions, governed by prescribed kernel moments, from resolved rigid particles, governed by low-order surface-traction moments and prescribed slip. The framework unifies these representations and shows how exterior-flow measurements provide information beyond drop translation, laying the foundation for constructing squirmer-like viscous drop solutions with controllable far-field behaviors.

physics.flu-dyn

Stability and equilibria of a compressible elastic membrane in Stokes flow

We formulate a continuum model for a compressible lipid-bilayer membrane immersed in Stokes flow, replacing exact local area inextensibility by conservation of an areal phospholipid density. The membrane free energy combines Helfrich bending, spontaneous curvature, and a finite area-compression penalty, so that membrane tension becomes a constitutive response to lipid-density variation rather than a Lagrange multiplier enforcing local area conservation. The resulting interfacial stress includes normal elastic forces and tangential Marangoni stresses generated by lipid redistribution; these stresses arise from membrane compressibility and can produce an effective negative tension when the local lipid density exceeds its preferred value. We further derive the linear stability of circular membranes in two dimensions and spherical membranes in three dimensions under full Stokes hydrodynamic coupling. In both cases, bending stabilizes the base shape, while excess lipid density destabilizes it by favoring increased membrane area. The first instability occurs in the lowest nontrivial shape mode, m = 2 in two dimensions and j = 2 in three dimensions. Energy expansions near onset show that the two-dimensional instability is a pitchfork bifurcation, whereas the three-dimensional instability is generically transcritical because prolate and oblate perturbations are geometrically distinct. These results provide a controlled compressible extension of classical vesicle mechanics and directly connect lipid-density variation, membrane tension, hydrodynamic coupling, and shape instability.

cond-mat.soft

Migration and deformation of a droplet enclosing an active particle

The encapsulation of active particles, such as bacteria or active colloids, inside a droplet gives rise to nontrivial shape dynamics and droplet motility. To understand this behavior, we derive an asymptotic solution for the fluid flow about a deformable droplet containing an active particle, modeled as a Stokes-flow singularity, in the case of small shape distortions. Offsetting of the active particle from the center of the drop breaks symmetry and leads to excitation of large number of shape modes as well as particle and drop displacement. Flows due to common singularity representations of active particles, such as Stokeslets, rotlets, and stresslets, are computed and compared to results for non-deformable droplets enclosing active particles. The effect of interfacial properties is also investigated. Surfactants adsorbed at the droplet interface immobilize the interface and arrest the droplet motion. Our results highlight strategies to steer the flows of active particles and create autonomously navigating containers.

cond-mat.soft

Hybrid plasmonic-photonic crystal formed on gel-immobilized colloidal crystal via solvent substitutio

Gel-immobilized colloidal crystals were prepared to obtain hybrid plasmonic-photonic crystals, in which electric field enhancement to a greater extent than that due to localized surface plasmons (LSP) alone was expected due to coupling between LSP and the photonic band. Polystyrene colloidal crystals immobilized by the N-(hydroxymethyl)acrylamide gel were immersed in an aqueous dispersion of gold nanoparticles (AuNPs). Then, the gel-immobilized colloidal crystals were picked out and immersed in an ionic liquid mixture. The surfaces of the gel-immobilized colloidal crystals immersed in the AuNP dispersion were observed via scanning electron microscopy after this solvent substitution. The lattice spacing of the colloidal crystal varied as the composition of the ionic liquid mixture was changed. The composition was determined so that the photonic band gap wavelength coincided with the LSP wavelength. Further, the reflection spectra were measured. Thus, we successfully prepared a hybrid plasmonic-photonic crystal.

cond-mat.soft

Nanostrucure of Hybrid Plasmonic-Potonic Crystal Formed on Gel-Immobilized Colloidal Crystal Observer by AFM after Drying

Aiming at fabrication of hybrid plasmonic-photonic crystals, gel-immobilized colloidal crystals made of a polystyrene colloidal suspension and an N-(Hydroxy methyl)acrylamid-based gel were immersed into an aqueous dispersion of gold nanoparticles. Atomic force microscope (AFM) observations have been performed for the gel-immobilized colloidal crystals with gold nanoparticles deposited on their surfaces. In the present study, the diameter of a colloidal sphere was c.a. 190 nm. The diameter of a gold nanoparticle was the same as in a preliminary study, c.a. 40 nm. Various immersion times up to two hours were tested. Surface of a sample of 2 hr immersion has been observed. Prior to the AFM observation, the sample was dried in a desiccator for 18 hrs. We have identified a face-centered cubic {111} structure of a colloidal crystal of nearly close packing. Nanoparticles isolated with one another have been observed on the surface of gel-immobilized crystal, which can be regarded as gold nanoparticles from their sizes.

cond-mat.mtrl-sci