Chan-Hee Jung

Active digital microfluidic paper chips with inkjet-printed patterned electrodes.

Active, paper-based, microfluidic chips driven by electrowetting are fabricated and demonstrated for reagent transport and mixing. Instead of using the passive capillary force on the pulp to actuate a flow of a liquid, a group of digital drops are transported along programmed trajectories above the electrodes printed on low-cost paper, which should allow point-of-care production and diagnostic activities in the future.

Synthesis of Li2TiO3 ceramic breeder powders by the combustion process

Abstract The synthesis of the ultra-fine Li 2 TiO 3 powder by the combustion reaction of lithium nitrate, titanium nitrate and specific fuels was investigated. Ultrafine Li 2 TiO 3 powders could be synthesized using glycine or a mixture of urea and citric acid. A pure Li 2 TiO 3 phase was obtained by the simple process without further calcination reaction. The specific surface area of the as-synthesized powder was 10 to 14 m 2 /g and the primary particle size was about 30 nm. The Li 2 TiO 3 body sintered at 800°C for 3 h had dense agglomerates which were formed by the inter-agglomerate sintering process. Each of the agglomerates consisted of very fine grains with a size of 0.3 to 0.5 μm.

Efficient immobilization and patterning of biomolecules on poly(ethylene terephthalate) films functionalized by ion irradiation for biosensor applications.

The surface of a poly(ethylene terephthalate) (PET) film was selectively irradiated with proton beams at various fluences to generate carboxylic acid groups on the surface; the resulting functionalized PET surface was then characterized in terms of its wettability, chemical structure, and chemical composition. The results revealed that (i) carboxylic acid groups were successfully generated in the irradiated regions of the PET surface, and (ii) their relative amounts were dependent on the fluence. A capture biomolecule, anthrax toxin probe DNA, was selectively immobilized on the irradiated regions on the PET surface. Cy3-labeled DNA as a target biomolecule was then hybridized with the probe DNA immobilized on the PET surface. Liver-cancer-specific α-fetoprotein (AFP) antigen, as a target biomolecule, was also selectively immobilized on the irradiated regions on the PET surface. Texas Red-labeled secondary antibody was then reacted with an AFP-specific primary antibody prebound to the AFP antigen on the PET surface for the detection of the target antigen, using an indirect immunoassay method. The results revealed that (i) well-defined micropatterns of biomolecules were successfully formed on the functionalized PET surfaces and (ii) the fluorescence intensity of the micropatterns was dependent mainly on the concentrations of the target DNA hybridized to the probe DNA and the target AFP antigen immobilized on the PET films. The lowest detectable concentrations of the target DNA and target AFP antigen in this study were determined to be 4 and 16 ng/mL, respectively, with the PET film prepared at a fluence of 5 × 10(14) ions/cm(2).

Surface Morphology Control of Polymer Films by Electron Irradiation and Its Application to Superhydrophobic Surfaces

A simple and controllable one-step method to fabricate superhydrophobic surfaces on poly(tetrafluoroethylene) (PTFE) films is developed on the base of electron irradiation. When the thickness of PTFE films is higher than the penetration depth of electron beams, electrical charging occurs at the surface of the films because of the imbalance between the accumulation of incident electrons and the emission of secondary electrons. Local inhomogeneity of charge distribution due to this electrical charging results in the nonuniform decomposition of PTFE molecular bonds. As electron fluence increases, surface morphology and surface roughness of the films are dramatically changed. An extremely rough surface with micrometer-sized pores is produced on the surface of PTFE films by electron irradiation at a fluence higher than 2.5 × 10(17) cm(-2).Because of high surface roughness, the irradiated PTFE films exhibit superhydrophobic property with a water contact angle (CA) greater than 150° at fluences ranging from 4 × 10(17) to 1 × 10(18) cm(-2). The surface morphology and corresponding water CA can be controlled by simply changing the electron fluence. This electron irradiation method can be applicable to the fabrication of superhydrophobic surfaces using other low-surface-energy materials including various fluoropolymers.

Poly(acrylic acid)-Grafted Fluoropolymer Films for Highly Sensitive Fluorescent Bioassays

In this study, a facile and effective method for the surface functionalization of inert fluoropolymer substrates using surface grafting was demonstrated for the preparation of a new platform for fluorescence-based bioassays. The surface of perfluorinated poly(ethylene-co-propylene) (FEP) films was functionalized using a 150 keV ion implantation, followed by the graft polymerization of acrylic acid, to generate a high density of carboxylic acid groups on the implanted surface. The resulting functionalized surface was investigated in terms of the surface density of carboxylic acid, wettability, chemical structure, surface morphology, and surface chemical composition. These results revealed that poly(acrylic acid) (PAA) was successfully grafted onto the implanted FEP surface and its relative amount depended on the fluence. To demonstrate the usefulness of this method for the fabrication of bioassays, the PAA-grafted FEP films were utilized for the immobilization of probe DNA for anthrax toxin, followed by hybridization with Cy3-labeled target DNA. Liver cancer-specific α-feto-protein (AFP) antigen was also immobilized on the PAA-grafted FEP films. Texas Red-labeled secondary antibody was reacted with AFP-specific primary antibody prebound to the AFP antigen using an immunoassay method. The results revealed that the fluorescence intensity clearly depended on the concentration of the target DNA hybridized to the probe DNA and the AFP antigen immobilized on the FEP films. The lowest detectable concentrations of the target DNA and the AFP antigen were 10 fg/mL and 10 pg/mL, respectively, with the FEP films prepared at a fluence of 3 × 10(14) ions/cm(2).

Efficient polymer solar cells with a solution-processed gold chloride as an anode interfacial modifier

The use of a solution-processed gold chloride (AuCl3) as an anode interfacial modifier was investigated for high-performance polymer solar cells (PSCs). Kelvin probe, 4-point probe, and X-ray photoelectron spectroscopy studies demonstrated that AuCl3 increases the indium-tin-oxide (ITO) work-function and decreases the ITO sheet resistance, because of Au nanoparticle formation and Cl adsorption by the AuCl3 treatment to induce a p-doping effect, thereby improving the built-in potential and interface resistance. As a result, the introduction of AuCl3 by simple solution processing remarkably improved cell-performances, indicating that AuCl3 is an efficient anode interfacial modifier for enhancing PSC-performance.

Patterning of biomolecules on a poly(ɛ-caprolactone) film surface functionalized by ion implantation

Biomolecule patterning is important due to its potential applications in biodevices, tissue engineering, and drug delivery. In this study, we developed a new method for a biomolecular patterning on poly(epsilon-caprolactone) (PCL) films based on ion implantation. Ion implantation on a PCL film surface resulted in the formation of carboxylic acid groups. The generated carboxylic acid groups were used for the covalent immobilization of amine-functionalized p-DNA, followed by hybridization with fluorescently tagged c-DNA. Biotin-amine was also covalently immobilized on the carboxylic acid generated PCL surfaces. Successful biotin-specific binding of streptavidin further confirmed the potential of this strategy for patterning of various biomolecules.

Simple and biocompatible micropatterning of multiple cell types on a polymer substrate by using ion implantation.

A noncytotoxic procedure for the spatial organization of multiple cell types remains as a major challenge in tissue engineering. In this study, a simple and biocompatible micropatterning method of multiple cell types on a polymer surface is developed by using ion implantation. The cell-resistant Pluronic surface can be converted into a cell-adhesive one by ion implantation. In addition, cells show different behaviors on the ion-implanted Pluronic surface. Thus this process enables the micropatterning of two different cell types on a polymer substrate. The micropatterns of the Pluronic were formed on a polystyrene surface. Primary cells adhered to the spaces of the bare polystyrene regions separated by the implanted Pluronic patterns. Secondary cells then adhered onto the implanted Pluronic patterns, resulting in micropatterns of two different cells on the polystyrene surface.

Photosensitive polymer brushes grafted onto PTFE film surface for micropatterning of proteins

Surface grafting of photosensitive polymer brushes on a flexible polymer surface was performed using Ar ion irradiation, which generated peroxides on the polymer surface upon exposure to air. These peroxides were utilized as initiators for graft polymerization of a photosensitive diazoketo-functionalized methacrylate monomer. Upon UV light exposure, the diazoketo group was converted into the carboxylic acid group which was used to covalently immobilize amine-functionalized biotin in a patterned fashion. Successful binding of streptavidin to the biotin-linked regions proved the potential of the platform for biomolecular patterning applications on commercial polymer substrates.

Eco-friendly and simple radiation-based preparation of graphene and its application to organic solar cells

We report the reduction of graphene oxide (GO) through an eco-friendly and simple radiation-based method and the practical application of the resulting radiation-reduced GO (RRGO) as a solution-processable hole-transporting layer (HTL) for organic solar cells. GO dispersed in N, N′-dimethylformamide (DMF) was irradiated by γ-rays at various absorbed doses. The analytical results revealed that GO in DMF was effectively reduced to RRGO by γ-ray irradiation-induced deoxygenation, and that the reduction degree was dependent on the absorbed dose. The electrical conductivity of RRGO increased up to 12.7xa0Sxa0cm−1 with an increase in the absorbed dose, whereas the work function decreased to 4.34xa0eV. An organic solar cell device with RRGO prepared at 50xa0kGy as an HTL exhibited the best performance, with a power conversion efficiency of 2.72%, which is a better cell efficiency than is possible in devices with conventional GO and solvothermally-reduced GO.