6 results on '"Junyong, Park"'
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2. Multifunctional Hierarchically-Assembled Hydrogel Particles with Pollen Grains via Pickering Suspension Polymerization
- Author
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Junyong Park and Patrick S. Doyle
- Subjects
Models, Molecular ,Materials science ,Molecular Conformation ,Nanoparticle ,Core (manufacturing) ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Polymerization ,Colloid ,Adsorption ,Suspensions ,Electrochemistry ,medicine ,General Materials Science ,Spectroscopy ,Water ,Hydrogels ,Surfaces and Interfaces ,Photochemical Processes ,021001 nanoscience & nanotechnology ,Condensed Matter Physics ,0104 chemical sciences ,Photopolymer ,Chemical engineering ,Pollen ,Suspension polymerization ,Swelling ,medicine.symptom ,0210 nano-technology ,Oils - Abstract
Hierarchical assembly of heterogeneous particles is of great importance to interface and colloid science. In this work, a facile but powerful approach for the large-scale production of multifunctional hydrogel particles armored with biological colloidal species is developed by combining Pickering stabilization and photopolymerization. Biocompatible hollow pollen grains extracted from naturally occurring pollen species with an average diameter of ∼32 μm serve as universal solid emulsifiers dispersed in an oil phase and are self-assembled at the interface between an oil phase and a photo-cross-linkable hydrogel to make water-in-oil (W/O) emulsion droplets. While droplets are solidified into hydrogel particles by UV-induced free-radical polymerization, self-assembled hollow pollen grains are transformed to a robust shell on hydrogel particles with supracolloidal structures. The physically adsorbed hollow pollen grains on the hydrogel core can be released by a hydration-induced swelling of hollow pollen grains, leading to a transient floating behavior of core-shell particles. The size of the resultant core-shell particles is easily controlled by tailoring the process parameters such as a liquid volume or a loading mass of hollow pollen grains. The incorporation of magnetic or upconverting luminescent nanoparticles into a hydrogel core successfully expands the functionality of core-shell particles that can provide new design opportunities for floating drug delivery or ecofriendly proppants.
- Published
- 2018
- Full Text
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3. Multifunctional Polymer Nanocomposites Reinforced by 3D Continuous Ceramic Nanofillers
- Author
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Jae-Wook Jung, Changui Ahn, Dongchan Jang, Jung-Wuk Hong, Sang Eon Lee, Sang-Min Kim, Taegeon Kim, Seung Min Han, Junyong Park, and Seokwoo Jeon
- Subjects
chemistry.chemical_classification ,Toughness ,Materials science ,Nanocomposite ,Fabrication ,Polymer nanocomposite ,General Engineering ,General Physics and Astronomy ,02 engineering and technology ,Polymer ,engineering.material ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Coating ,chemistry ,visual_art ,engineering ,visual_art.visual_art_medium ,General Materials Science ,Ceramic ,Composite material ,0210 nano-technology ,Porosity - Abstract
Polymer nanocomposites with inclusion of ceramic nanofillers have relatively high yield strength, elastic moduli, and toughness that therefore are widely used as functional coating and films for optoelectronic applications. Although the mechanical properties are enhanced with increasing the fraction of nanofiller inclusion, there generally is an upper limit on the amount of nanofiller inclusion because the aggregation of the fillers in the polymer matrix, which typically occurs, degrades the mechanical and/or optical performances above 5 vol % of inclusions. Here, we demonstrate an unconventional polymer nanocomposite composed of a uniformly distributed three-dimensional (3D) continuous ceramic nanofillers, which allows for extremely high loading (∼19 vol %) in the polymer matrix without any concern of aggregation and loss in transparency. The fabrication strategy involves conformal deposition of Al2O3 nanolayer with a precise control in thickness that ranges from 12 to 84 nm on a 3D nanostructured porous...
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- 2018
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4. Two-Dimensional WO3 Nanosheets Chemically Converted from Layered WS2 for High-Performance Electrochromic Devices
- Author
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Bumsoo Kim, Travis G. Novak, Ashraful Azam, Junyong Park, Seokwoo Jeon, Anand P. Tiwari, Sung Ho Song, and Jungmo Kim
- Subjects
Materials science ,Mechanical Engineering ,Tungsten disulfide ,Intercalation (chemistry) ,Tungsten oxide ,Bioengineering ,02 engineering and technology ,General Chemistry ,Crystal structure ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Condensed Matter Physics ,Electrochromic devices ,Electrochemistry ,01 natural sciences ,0104 chemical sciences ,chemistry.chemical_compound ,chemistry ,Transition metal ,Chemical engineering ,Electrochromism ,General Materials Science ,0210 nano-technology - Abstract
Two-dimensional (2D) transitional metal oxides (TMOs) are an attractive class of materials due to the combined advantages of high active surface area, enhanced electrochemical properties, and stability. Among the 2D TMOs, 2D tungsten oxide (WO3) nanosheets possess great potential in electrochemical applications, particularly in electrochromic (EC) devices. However, feasible production of 2D WO3 nanosheets is challenging due to the innate 3D crystallographic structure of WO3. Here we report a novel solution-phase synthesis of 2D WO3 nanosheets through simple oxidation from 2D tungsten disulfide (WS2) nanosheets exfoliated from bulk WS2 powder. The complete conversion from WS2 into WO3 was confirmed through crystallographic and elemental analyses, followed by validation of the 2D WO3 nanosheets applied in the EC device. The EC device showed color modulation of 62.57% at 700 nm wavelength, which is 3.43 times higher than the value of the conventional device using bulk WO3 powder, while also showing enhanceme...
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- 2018
- Full Text
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5. Sequestration-Mediated Downregulation of de Novo Purine Biosynthesis by AMPK
- Author
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Danielle L. Schmitt, Junyong Park, Songon An, and Yun-ju Cheng
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0301 basic medicine ,Purine ,Green Fluorescent Proteins ,Down-Regulation ,AMP-Activated Protein Kinases ,Biochemistry ,Article ,03 medical and health sciences ,chemistry.chemical_compound ,AMP-activated protein kinase ,Downregulation and upregulation ,Humans ,Protein kinase A ,Purine metabolism ,chemistry.chemical_classification ,030102 biochemistry & molecular biology ,biology ,AMPK ,General Medicine ,Cell biology ,030104 developmental biology ,Enzyme ,chemistry ,Purines ,biology.protein ,Molecular Medicine ,Flux (metabolism) ,HeLa Cells - Abstract
Dynamic partitioning of de novo purine biosynthetic enzymes into multienzyme compartments, purinosomes, has been associated with increased flux of de novo purine biosynthesis in human cells. However, we do not know of a mechanism by which de novo purine biosynthesis would be downregulated in cells. We have investigated the functional role of AMP-activated protein kinase (AMPK) in the regulation of de novo purine biosynthesis because of its regulatory action on lipid and carbohydrate biosynthetic pathways. Using pharmacological AMPK activators, we have monitored subcellular localizations of six pathway enzymes tagged with green fluorescent proteins under time-lapse fluorescence single-cell microscopy. We revealed that only one out of six pathway enzymes, formylglycinamidine ribonucleotide synthase (FGAMS), formed spatially distinct cytoplasmic granules after treatment with AMPK activators, indicating the formation of single-enzyme self-assemblies. In addition, subsequent biophysical studies using fluorescence recovery after photobleaching showed that the diffusion kinetics of FGAMS were slower when it localized inside the self-assemblies than within the purinosomes. Importantly, high-performance liquid chromatographic studies revealed that the formation of AMPK-promoted FGAMS self-assembly caused the reduction of purine metabolites in HeLa cells, indicating the downregulation of de novo purine biosynthesis. Collectively, we demonstrate here that the spatial sequestration of FGAMS by AMPK is a mechanism by which de novo purine biosynthesis is downregulated in human cells.
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- 2016
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6. Flexible Near-Field Nanopatterning with Ultrathin, Conformal Phase Masks on Nonplanar Substrates for Biomimetic Hierarchical Photonic Structures
- Author
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Suck Won Hong, Junyong Park, Seok Hee Kang, Hyowook Kim, Seokwoo Jeon, Jonghwa Shin, Taehoon Kim, and Youngwoo Kwon
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Nanostructure ,Materials science ,Fabrication ,business.industry ,General Engineering ,General Physics and Astronomy ,Near and far field ,Nanotechnology ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,0104 chemical sciences ,Phase (matter) ,Nano ,General Materials Science ,Wafer ,Nanodot ,Photonics ,0210 nano-technology ,business - Abstract
Multilevel hierarchical platforms that combine nano- and microstructures have been intensively explored to mimic superior properties found in nature. However, unless directly replicated from biological samples, desirable multiscale structures have been challenging to efficiently produce to date. Departing from conventional wafer-based technology, new and efficient techniques suitable for fabricating bioinspired structures are highly desired to produce three-dimensional architectures even on nonplanar substrates. Here, we report a facile approach to realize functional nanostructures on uneven microstructured platforms via scalable optical fabrication techniques. The ultrathin form (∼3 μm) of a phase grating composed of poly(vinyl alcohol) makes the material physically flexible and enables full-conformal contact with rough surfaces. The near-field optical effect can be identically generated on highly curved surfaces as a result of superior conformality. Densely packed nanodots with submicron periodicity are uniformly formed on microlens arrays with a radius of curvature that is as low as ∼28 μm. Increasing the size of the gratings causes the production area to be successfully expanded by up to 16 in(2). The "nano-on-micro" structures mimicking real compound eyes are transferred to flexible and stretchable substrates by sequential imprinting, facilitating multifunctional optical films applicable to antireflective diffusers for large-area sheet-illumination displays.
- Published
- 2016
- Full Text
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