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Gi-Ra Yi

Publications and source records attributed to Gi-Ra Yi.

8 recordsLinked to original sources

Microwave-assisted self-organization of colloidal particles in confining aqueous droplets.

Monodisperse aqueous emulsion droplets encapsulating colloidal particles were produced in the oil phase, and controlled microwave irradiation of the aqueous drop phase created spherical colloidal crystals by so-called evaporation-induced self-organization of the colloidal particles. Unlike usual colloidal crystals, colloidal crystals in spherical symmetry (or photonic balls) possessed photonic band gaps for the normal incident light independent of the position all over the spherical surface. While the consolidation of colloidal particles in emulsion droplets in an oven took several hours, the present microwave-assisted evaporation could reduce the time for complete evaporation to a few tens of minutes. Under the microwave irradiation, the aqueous phase in emulsions was superheated selectively and the evaporation rate of water could be controlled easily by adjusting the microwave intensity. The result showed that the packing quality of colloidal crystals obtained by the microwave-assisted self-organization was good enough to show photonic band gap characteristics. The reflectance of our photonic balls responded precisely to any change in physical properties including the size of colloidal particles, refractive index mismatch, and angle of the incident beam. In particular, for polymeric particles, the photonic band gap could be tuned by the intensity of microwave irradiation, and the reflection color was red-shifted with stronger microwave irradiation. Finally, for better photonic band gap properties, inverted photonic balls were prepared by using the spherical colloidal crystals as sacrificial templates.

Journal Article↗

Close-packed hemispherical microlens array from two-dimensional ordered polymeric microspheres.

This paper describes a facile, reproducible soft-lithography-based method for fabricating hexagonally close-packed microlens arrays by templating the surface of a colloidal monolayer, which is formed by spin-casting monodisperse polystyrene microspheres. The relief structure of colloidal monolayers has successfully generated PDMS elastomers with hexagonal arrays of hemispherical air voids. Closely packed hemispherical microlens arrays were imprinted on ultraviolet-curable photopolymers which are bound on glass substrates. Atomic force microscopy measurements showed that each spherical hole of the PDMS molds is 103 nm deep and the replicated microlens is 95 nm in height with narrow size distribution and good reproducibility. Without a multistep engineering process, this method might provide a reliable route to fabricate embossed thin layers ranging from nanometer to micrometers by controlling the size of polymer microspheres over a centimeter scale area.

Journal Article↗

High-speed fabrication of patterned colloidal photonic structures in centrifugal microfluidic chips.

In this paper, we report a rapid and facile method for fabricating colloidal photonic crystals inside microchannels of radially symmetric microfluidic chips which were made using soft-lithography. As the suspension of monodisperse silica or polystyrene latex spheres was driven to flow through the channels under the action of centrifugal force, the colloidal spheres were quickly assembled into face centered cubic arrangement which had a few photonic stop bands. The soft-microfluidic channels and cells confined the colloidal crystals into designed patterns. The optical reflectance was modulated by the refractive-index mismatch between the colloidal particles and the solvent in the interstices between the particles. Therefore, the present microfluidic chips with built-in colloidal photonic crystals can be used as in-situ optofluidic microsensors for high throughput screening or light filters in integrated adaptive optical devices.

Colloids↗

Fabrication of one-dimensional colloidal assemblies from electrospun nanofibers.

Electrospun nanofibers were used as confining geometries for fabricating 1-D colloidal assemblies. Silica particles dispersed in several different polymer solutions were cast into nanofibers by an electrospinning process. The silica particle configurations were examined in terms of the size ratio of silica particles to nanofibers and the properties of the dispersing medium. As the electrospun fiber was extended highly, the silica particles dispersed in the polymer solution began to assemble spontaneously into a pearl-necklace structure. We also demonstrated the alignment of 1-D silica assemblies using a designed configuration of collector electrodes.

Chemistry↗

Self-organization of bidisperse colloids in water droplets.

Most of the colloidal clusters have been produced from oil-in-water emulsions with identical microspheres dispersed in oil droplets. Here, we present new types of binary colloidal clusters from phase-inverted water-in-oil emulsions using various combinations of two different colloids with several size ratios: monodisperse silica or polystyrene microspheres for larger particles and silica or titania nanoparticles for smaller particles. Obviously, a better understanding of how finite groups of different colloids self-organize in a confined geometry may help us control the structure of matter at multiple length scales. In addition, since aqueous dispersions have much better phase stability, we could produce much more diverse colloidal materials from water-in-oil emulsions rather than from oil-in-water emulsions. Interestingly, the configurations of the large microspheres were not changed by the presence of the small particles. However, the arrangement of the smaller particles was strongly dependent on the nature of the interparticle interactions. The experimentally observed structural evolutions were consistent with the numerical simulations calculated using Surface Evolver. These clusters with nonisotropic structures can be used as building blocks for novel colloidal structures with unusual properties or by themselves as light scatterers, diffusers, and complex adaptive matter exhibiting emergent behavior.

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Connected open structures from close-packed colloidal crystals by hyperthermal neutral beam etching.

We report the fabrication of connected open structures from close-packed colloidal crystals by hyperthermal neutral beam etching. Colloidal crystal films of polystyrene microspheres were prepared by a vertical deposition method. Exposure of the colloidal crystal films to hyperthermal neutral beam made isolated microspheres in the face-centered cubic lattice, each of which was connected with its twelve nearest neighbors through very thin cylinders. Due to the charge neutrality of impinging gas molecules of the hyperthermal neutral beam, the spherical shape of polymer microspheres was almost maintained during the etching process. The Bragg reflection peaks were modulated by the etched volume of colloidal crystals. Finally, the inverse structures of such open structures were replicated by a simple room-temperature chemical vapor deposition and subsequently burning out polymer template spheres.

Colloids↗

Fabrication of hollow colloidal crystal cylinders and their inverted polymeric replicas.

We fabricated colloidal crystals on a fiber by a dip-coating method. The self-assembly of monodisperse colloidal particles was affected by the curvature of the fiber (the reciprocal of the fiber radius). As the fiber became smaller in diameter, fewer layers of the colloidal spheres were coated for a given lift-up speed. The hollow colloidal crystal cylinders were used as a template for creating macroporous structure having three-dimensionally interconnected air cavities. Specifically, the polymer precursor was infiltrated into the colloidal crystal template and the macroporous polymer structures were obtained after the selective etching of colloidal particles.

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Packings of uniform microspheres with ordered macropores fabricated by double templating.

Highly uniform 3-D ordered macroporous spheres in regular arrays were produced by a double templating process. The first template of larger silica balls produced the polymer skeleton for guiding the shape and size of the self-assembled superstructure of smaller polymeric balls, which are introduced subsequently into the internal space of the skeleton. The second templating with inorganic precursors has created novel superstructured materials, which could open up significant opportunities in a variety of areas ranging from absorbents/catalysts to novel photonic crystals.

Journal Article↗