Publications by authors named "Young Gyu Jeong"

High-performance electromagnetic interference (EMI) shielding materials with high flexibility, low density, and hydrophobic surface are crucial for modern integrated electronics and telecommunication systems in advanced industries like aerospace, military, artificial intelligence, and wearable electronics. In this study, we present flexible and hydrophobic MXene/Ni-coated polyester (PET) fabrics featuring a double-layered structure, fabricated via a facile and scalable dip-dry coating process followed by electroless nickel plating. Increasing the dip-dry coating iterations up to 10 cycles boosts the MXene loading content (∼31 wt %) and electrical conductivity (∼86 S/cm) of MXene-coated PET fabrics, while maintaining constant porosity (∼95%).

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Liposomes are microspheres produced by placing phospholipids in aqueous solutions. Liposomes have the advantage of being able to encapsulate both hydrophilic and hydrophobic functional substances and are thus important mediators used in cosmetics and pharmaceuticals. It is important for liposomes to have small sizes, uniform particle size distribution, and long-term stability.

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To attain eco-friendly polyurethane composites with enhanced thermal and mechanical properties, in this study, a series of cationic waterborne polyurethane (cWPU) nanocomposite films reinforced with 1-50 wt% chitin nanofiber (ChNF) loadings was fabricated by a facile aqueous dispersion casting. The microstructure, thermal and mechanical properties of the nanocomposite films were investigated by considering the loading content and the interfacial interaction of ChNF in the cWPU matrix. For the purpose, a hard/soft segmented cWPU with an average particle size of ∼151 nm in aqueous dispersion was synthesized by using poly(tetramethylene glycol), isophorone diisocyanate, N-methyldiethanolamine, and 1,4-butanediol.

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In this study, a series of thermotropic liquid crystalline polyester (TLCP)-based blends containing 1-30 wt% poly(ethylene--glycidyl methacrylate) (PEGMA) were fabricated by masterbatch-assisted melt-compounding. The scanning electron microscopy (SEM) images showed a uniformly dispersed microfibrillar structure for the TLCP component in cryogenically-fractured blends, without any phase-separated domains. The FT-IR spectra showed that the carbonyl stretching bands of TLCP/PEGMA blends shifted to higher wavenumbers, suggesting the presence of specific interactions and/or grafting reactions between carboxyl/hydroxyl groups of TLCP and glycidyl methacrylate groups of PEGMA.

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We report the microstructure and thermoelectric properties of composite nanofiber webs, which were fabricated by dual-electrospinning of polyacrylonitrile (PAN) and sodium cobalt oxide (NaCoO) precursor solutions with different input compositions and following heat-treatment at 600-900 °C for simultaneous carbonation and calcination. The SEM and EDS mapping images revealed that PAN-derived carbon nanofibers (CNFs) and NaCoO-based ceramic nanofibers coexisted in the composite nanofiber webs and that their relative contents could be controlled by the input compositions. The Seebeck coefficient increased from ~26.

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We conducted a preliminary study on fiber structural development in the high-speed melt spinning of environmentally friendly polyethylene terephthalate (Ti-PET) synthesized with 25 ppm of titanium-based catalyst, which was compared with conventional PET (Sb-PET) synthesized with 260 ppm of antimony-based catalyst. Gel permeation chromatography of Ti- and Sb-PET resins of intrinsic viscosity 0.63 confirmed that both resins have similar molecular weights and distributions.

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We herein report the effects of carboxymethylated cellulose nanofibril (c-CNF) on the microstructure, thermal and mechanical properties of waterborne polyurethane (WPU)-based nanocomposite films. For the purpose, an aqueous dispersion of hard/soft segmented WPU with a mean particle size of ∼169 nm was manufactured by using poly(propylene glycol), isophorone diisocyanate, 2,2-dimethylolpropionic acid and 1,4-butanediol. WPU nanocomposite films with 1-50 wt% c-CNF loadings were then manufactured via an efficient casting method.

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For attaining eco-friendly nanocellulose-based films with enhanced thermal and mechanical properties, a series of composite films was fabricated by using a facile casting method of aqueous carboxymethylated cellulose nanofibril (c-CNF) dispersions with different contents (0-20 wt%) of polyacrylamide (PAM). The microstructure, thermal and mechanical properties of c-CNF/PAM composite films were investigated as a function of the PAM content. The FT-IR spectra revealed the presence of specific interactions between c-CNF and PAM in the composite films.

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In this study, pyrolyzed photoresist films (PPFs) were prepared using commercial SU8 photoresist by proton irradiation and pyrolysis. SU8 thin films were irradiated with high-energy proton ions and then pyrolyzed in a tube furnace at 1000 °C under inert atmosphere. The carbonization yield of the PPFs increased with an increasing fluence due to the formation of more crosslinked network structures at a higher fluence.

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Piezoelectric nanogenerators, harvesting energy from mechanical stimuli in our living environments, hold great promise to power sustainable self-sufficient micro/nanosystems and mobile/portable electronics. BaTiO3 as a lead-free material with high piezoelectric coefficient and dielectric constant has been widely examined to realize nanogenerators, capacitors, sensors, etc. In this study, polydimethylsiloxane (PDMS)-based flexible composites including BaTiO3 nanofibers with different alignment modes were manufactured and their piezoelectric performance was examined.

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We fabricated silver nanowire (AgNW)-coated cellulose papers with a hierarchical structure by an efficient and facile dip-coating process, and investigated their microstructures, electrical conductivity and electromagnetic interference (EMI) shielding effectiveness. SEM images confirm that AgNWs are coated dominantly on the paper surfaces, although they exist partially in the inner parts of the cellulose papers, which demonstrates that the AgNW density gradually decreases in thickness direction of the AgNW/cellulose papers. This result is supported by the anisotropic apparent electrical conductivity of the AgNW/cellulose papers depending on in-plane or thickness direction.

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We have manufactured regenerated cellulose-based composite films reinforced with pristine multiwalled carbon nanotube (MWCNT) by a facile casting of cellulose/DMAc/LiCl solutions containing 0.2-10.0wt% MWCNT and have investigated their application as electric heating materials by examining microstructure, thermal stability, and electrical properties.

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We report microstructure of thermomechanically stable multiwalled carbon nanotube (MWCNT)/poly(m-phenylene isophthalamide) (m-aramid) composite films containing 0.0-10.0 wt % MWCNTs and their performance as electric heating elements.

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The crystallization behavior and the orientation of linear alkane hentetracontane (C41) confined in cylindrical nanoporous alumina templates with different surface energies were investigated by nonisothermal crystallization and X-ray diffraction. The surface of pristine nanoporous alumina was modified to have low surface energy by grafting with polydimethylsiloxane. In the pristine nanoporous alumina, C41 crystallized at two crystallization temperature ranges, lower than bulk, and exhibited the decreased Avrami exponents.

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Superhydrophobic poly(lactic acid) (PLA) fabrics are prepared by UV photo-grafting of hydrophobic silica particles possessing vinyl functional groups on the surfaces, which is a novel one-step process to provide surface with roughness as well as hydrophobicity simultaneously. For this purpose, hydrophobic silica particles with vinyl groups and average diameter of 1.51+/-0.

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When heated above room temperature, some crystalline polymorphs of the 1,3-bis(hydroxyalkylamino)-4,6-dinitrobenzenes (BDBn, n = 2-5), bis(hydroxyalkyl) analogues of the intramolecular charge-transfer molecule 1,3-diamino-4,6-dinitrobenzene, exhibit "dual" thermochromism: gradual color change from yellow to orange at lower temperatures, and sharp color change from orange to red at higher temperatures. These two thermochromic changes are related to different solid-state processes. When allowed to cool to room temperature, the yellow color of the thermochromic molecules with different alkyl length (n) is recovered with unexpectedly different kinetics, the order of the respective rate constants ranging from 10(-7)-10(-6) s(-1) for BDB2 to about 0.

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To obtain the superhydrophobic water-repellent cotton fabrics, cotton fabrics were treated with silica nanoparticles and/or a cost-effective water-repellent agent (WR agent). Two different silica nanoparticles were synthesized via a sol-gel process and their shapes, sizes, and compositions were characterized. It was found that silica particles are spherical and have diameters of 143 and 378 nm.

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We report the synthesis of hydroxyapatite/polyacrylamide (HAp/PAAm) composite hydrogels with various HAp contents by free radical polymerization and their removal capability of Pb(2+) ions in aqueous solutions with controlled initial Pb(2+) ion concentrations and pH values of 2-5. The swelling ratio of the composite gels in aqueous solutions decreases with increasing the HAp content in the gels. The composite gel with higher HAp content exhibits the higher removal capacity of Pb(2+) ions owing to the higher adsorption sites for Pb(2+) ions, but shows the slower removal rate of Pb(2+) ions due to the lower degree of swelling.

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We have prepared hydroxyapatite/polyurehthane (HAp/PU) composite foams with two different HAp contents of 20 and 50 wt.% and investigated their removal capability of Pb2+ ions from aqueous solutions with various initial Pb2+ ion concentrations and pH values of 2-6. HAp/PU composite foams synthesized exhibited well-developed open pore structures which provide paths for the aqueous solution and adsorption sites for Pb2+ ions.

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The crystallization of monodisperse linear polyethylene confined in nanoporous alumina is investigated with the calorimetric measurements. We observe a drastic change in crystallization behavior, specifically nucleation, with a decrease in the pore diameter. Crystallization in relatively larger pores with the diameters of 62 and 110 nm occurs at lower temperatures within a very narrow range, whereas crystallization in smaller pores with diameters of 15-48 nm occurs at a higher and broad range of temperatures.

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The influence of copolymer configuration on the phase behavior of various ternary polymer blends containing a crystallizable polyester, a noncrystallizable polyether, and an acrylic random copolymer of different chain configuration was investigated. In these ternary blends, the acrylic random copolymer is typically added to control rheological properties at elevated temperatures. In fact, the acrylic random copolymers composed of various compositions of MMA and nBMA were found to have different miscibility with polyester as well as polyether, leading to substantially different phase behavior of ternary blends.

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