Publications by authors named "Junpei Yamanaka"

In this study, we demonstrate a novel and efficient fabrication methodology for nonclose-packed, two-dimensional (2D) colloidal crystals exhibiting square lattice structures. In our recent work, we detailed the formation of 2D colloidal crystals via the electrostatic adsorption of three-dimensional (3D) charged colloidal crystals onto oppositely charged substrates. These 3D colloidal crystals possessed a face-centered cubic (FCC) lattice structure with their (111) planes aligned parallel to the substrate, facilitating the formation of 2D crystals with triangular lattice arrangements upon adsorption.

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We have showcased the potential of polymerized hydrogels (PGMs) with uniform-sized stimuli-responsive microgel particles as promising alternatives to prevent aggregation in solution based nanoparticle systems. In the current work, we implemented the PGM concept by embedding anionic stimuli-responsive microgels (PNIPAM-co-AAc)-silver (Ag) hybrids within a hydrogel matrix. These PGM@AgNP hybrid materials are used as catalysts for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) in the presence of sodium borohydride.

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We report here that a two-dimensional (2D) diamond-like structure of micron-sized colloidal particles can be obtained by layer-by-layer self-assembly. Positively and negatively charged silica particles, 1 μm in diameter, were used in the experiments. On a positively charged, flat glass substrate, the first layer of negatively charged particles was prepared to form a non-close-packed 2D crystal.

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We conducted a charge-charge clustering experiment of positively and negatively charged colloidal particles in aqueous media under a microgravity environment at the International Space Station. A special setup was used to mix the colloid particles in microgravity and then these structures were immobilized in gel cured using ultraviolet (UV) light. The samples returned to the ground were observed by optical microscopy.

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The free electrons inside precious metals such as Au vibrate when the surface of the metal is irradiated with an electromagnetic wave of an appropriate frequency. This oscillation is referred to as surface plasmon resonance (SPR), and the resonance frequency varies with permittivity of the medium around the metal. SPR sensors are widely applied in the fields of bioscience and pharmaceutical sciences, including biosensing for drug discovery, biomarker screening, virus detection, and testing for food safety.

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Hypothesis: The colloidal epitaxy utilizing a patterned substrate is used to fabricate colloidal crystals of the same structure and lattice spacing with the substrate, which is an effective technique for creating desired nanoscale architectures. However, this technique has been mainly limited to a single-component system. The colloidal epitaxy is versatile if multicomponent colloidal crystals can be produced, which is inspired by our previous study regarding binary colloidal crystals (b-CCs) fabricated at the edge of single-component crystals.

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We report that the aqueous dispersions of negatively charged submicron-sized colloidal Au particles formed non-close-packed colloidal crystals by the addition of a like-charged linear polyelectrolyte, sodium polyacrylate (NaPAA). Au particles often form irregular aggregates in dispersions because of a strong van der Waals force acting between them. To prevent aggregation, we introduced negative electric charges on particle surfaces.

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Article Synopsis
  • The study focuses on how solution flow impacts the growth and properties of colloidal crystals, particularly in terms of achieving high crystallinity and large-area formations.
  • Three main effects of solution flow were observed: it enlarges the initial layer of particles, aids in forming superlattice structures in mixed particle systems, and leads to the creation of a new circular packing arrangement.
  • The research suggests that controlling flow dynamics can improve the self-assembly process and ultimately enhance the quality of colloidal crystals.
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Article Synopsis
  • This study shows that you can create nonclose-packed 2D colloidal crystals on solid surfaces using charged 3D crystals attracted to oppositely charged substrates.
  • They achieved this by adsorbing a single layer of negatively charged polystyrene and silica particles onto a glass surface treated with a cationic silane.
  • The method resulted in large, uniform 2D crystals with consistent interparticle distances, and it also produced 2D gold crystals, potentially useful for applications in plasmonics.
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A mechanism for diffusiophoresis of a charged colloidal particle undergoing surface chemical reaction is proposed. A theoretical model is constructed to describe the dynamics of the particle and the surrounding solution of a weak electrolyte. Theoretical analysis and numerical simulations of the model reveal that phoretic motion of the particle emerges in response to a concentration gradient of electrolyte.

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The risk of rheumatoid arthritis (RA) is linked to environmental and genetic factors. Cigarette smoking is an established environmental risk factor for the disease that contributes to its development and severity. Previously, we found that cigarette smoke condensate (CSC), both mainstream and sidestream, aggravates collagen type II-induced arthritis (CIA), which was observed following either intraperitoneal inoculation or nasal exposure.

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Particle adhesion onto hydrogels has recently attracted considerable attention because of the potential biomedical applications of the resultant materials. A variety of interactions have been taken advantage of for adsorption, including electrostatic forces, hydrophobic interactions and hydrogen bonding. In this study, we report significant adsorption of submicron-sized silica particles onto hydrogel surfaces in water, purely by van der Waals (vdW) attraction.

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Understanding nucleation dynamics is important both fundamentally and technologically in materials science and other scientific fields. Two-dimensional (2D) nucleation is the predominant growth mechanism in colloidal crystallization, in which the particle interaction is attractive, and has recently been regarded as a promising method to fabricate varieties of complex nanostructures possessing innovative functionality. Here, polymers are added to a colloidal suspension to generate a depletion attractive force, and the detailed 2D nucleation process on the terrace of the colloidal crystals is investigated.

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Article Synopsis
  • The study focuses on how oppositely charged colloidal particles form clusters, using numerical simulations based on Brownian dynamics and a Yukawa potential.
  • It identifies an equilibrium phase where clusters coexist with unassociated particles, revealing that the number and shape of clusters are influenced by the particles' charge numbers and ratios.
  • The research also establishes a phase diagram for cluster formations and shows that clusters can develop a multilayer structure when there's a high charge ratio, indicating dynamic changes in cluster-particle interactions during the formation process.
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Crystallization of colloids has extensively been studied for past few decades as models to study phase transition in general. Recently, complex crystal structures in multi-component colloids, including alloy and eutectic structures, have attracted considerable attention. However, the fabrication of 2D area-filling colloidal eutectics has not been reported till date.

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Article Synopsis
  • Charged colloids undergo thermoreversible crystallization as ionic surfactants adsorb onto their surfaces, causing them to crystallize when cooled and melt when heated.
  • The study used polystyrene particles in mixtures of ethylene glycol and water, allowing for modulation of surfactant adsorption by adjusting the ethylene glycol concentration.
  • Changes in ionic strength due to the temperature-dependent concentration of non-adsorbed surfactants were found to drive this crystallization and melting behavior, with implications for controlling colloidal materials in lower permittivity environments.
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We report on the controlled clustering of oppositely charged colloidal particles by the adsorption of ionic surfactants, which tunes charge numbers Z of particles. In particular, we studied the heteroclustering of submicron-sized polystyrene (PS) and silica particles, both of which are negatively charged, in the presence of cetylpyridinium chloride (CPC), a cationic surfactant. The surfactant concentration Csurf was selected below the critical micelle concentration.

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Phase-separation dynamics of weakly charged polyacid solutions under a constant gradient of base concentration is studied both theoretically and numerically. The time-evolution equation of polymer volume fraction is derived by assuming that the chemical equilibrium of the dissociation reaction is locally established. Numerical simulations of the system in contact with two reservoirs in which the base concentrations differ are performed.

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Uniformly shaped, charged colloidal particles dispersed in water form ordered "crystal" structures when the interaction between the particles is sufficiently strong. Herein, we report the behavior of "impurity" particles, whose sizes and/or charge numbers are different from those of the bulk, on addition to the charged colloidal crystals. These impurities were excluded from the crystals during the homogeneous crystallization, crystal grain growth, and unidirectional crystallization processes.

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We examined the application of recrystallization and zone-melting crystallization methods, which have been used widely to fabricate large, high-purity crystals of atomic and molecular systems, to charged colloidal crystals. Our samples were aqueous dispersions of colloidal silica (with particle diameters of d = 108 or 121 nm and particle volume fractions of ϕ = 0.035-0.

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We have found that an impurity partitioning takes place during growth of colloidal crystals, which was recognized by the fact that the impurity concentration in the solid (CS) was different from that in the initial solution (C0). The effective partition coefficient k(eff) (=CS/C0) was investigated for pure polystyrene and polystyrene dyed with fluorescent particles by changing the ratio of particle diameters d(imp)/d(cryst) and growth rate V. At each size ratio for the polystyrene impurity, k(eff) was less than unity and increased to unity with increasing V, whereas at a given growth rate, k(eff) increased to unity as d(imp)/d(cryst) approached unity.

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We examine the compression of charged colloidal crystals under the influence of gravitational force by monitoring the spatiotemporal variations of Bragg diffraction from the crystal lattice. We use the dilute aqueous dispersions of colloidal silica particles (diameter=216 nm, charge number=733, a particle volume fraction φ=0.06) in the presence of 5-15 μM sodium chloride.

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We examine the spatial distribution of fluorescent-labeled charged polystyrene (PS) particles (particle volume fraction ϕ = 0.0001 and 0.001, diameter d = 183 and 333 nm) added to colloidal crystals of charged silica particles (ϕ = ϕ(s) = 0.

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We examine influence of temperature on the phase behavior of dilute aqueous dispersions of charged colloidal silica and polystyrene particles. They undergo either freezing or melting transitions with increasing temperature. Freezing occurs in the case of low-charge, low-salt colloids, and melting is observed in the case of high-charge, high-salt colloids.

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