Taesung Kim

Low‐Temperature Synthesis of Large‐Scale Molybdenum Disulfide Thin Films Directly on a Plastic Substrate Using Plasma‐Enhanced Chemical Vapor Deposition

By plasma-enhanced chemical vapor deposition, a molybdenum disulfide (MoS2 ) thin film is synthesized directly on a wafer-scale plastic substrate at below 300 °C. The carrier mobility of the films is 3.74 cm(2) V(-1) s(-1) . Also, humidity is successfully detected with MoS2 -based sensors fabricated on the flexible substrate, which reveals its potential for flexible sensing devices.

Fiber optic sensors for temperature monitoring during thermal treatments: An overview

During recent decades, minimally invasive thermal treatments (i.e., Radiofrequency ablation, Laser ablation, Microwave ablation, High Intensity Focused Ultrasound ablation, and Cryo-ablation) have gained widespread recognition in the field of tumor removal. These techniques induce a localized temperature increase or decrease to remove the tumor while the surrounding healthy tissue remains intact. An accurate measurement of tissue temperature may be particularly beneficial to improve treatment outcomes, because it can be used as a clear end-point to achieve complete tumor ablation and minimize recurrence. Among the several thermometric techniques used in this field, fiber optic sensors (FOSs) have several attractive features: high flexibility and small size of both sensor and cabling, allowing insertion of FOSs within deep-seated tissue; metrological characteristics, such as accuracy (better than 1 °C), sensitivity (e.g., 10 pm·°C−1 for Fiber Bragg Gratings), and frequency response (hundreds of kHz), are adequate for this application; immunity to electromagnetic interference allows the use of FOSs during Magnetic Resonance- or Computed Tomography-guided thermal procedures. In this review the current status of the most used FOSs for temperature monitoring during thermal procedure (e.g., fiber Bragg Grating sensors; fluoroptic sensors) is presented, with emphasis placed on their working principles and metrological characteristics. The essential physics of the common ablation techniques are included to explain the advantages of using FOSs during these procedures.

Reduction of metal contact resistance of graphene devices via CO2 cluster cleaning

We report on a cleaning technique using CO2 clusters for large-scale mono-layer graphene fabricated via chemical vapor deposition (CVD) and its application to reduce contact resistance of the CVD graphene device. We found that polymeric residues, i.e., polymethyl methacrylate and photoresist which are generated during transfer and patterning of graphene, can be effectively removed via rapid shrinkage, induced by thermal energy transfer to low temperature CO2 clusters. By applying the CO2 clusters to the cleaning of the interface between metal and graphene, the metal contact resistance of the fabricated graphene field effect transistor was lowered to 26.6% of pristine graphene. The contact resistance shows the best result at an optimized CO2 cluster cleaning condition with a flow rate of 20u2009l/min, and the resistance was further lowered to 270 Ω μm when a gate bias of −40u2009V was applied. We expect that the proposed CO2 cluster cleaning to be a very promising technique for future device application using 2-di...

Construction and characterization of Cu2+, Ni2+, Zn2+, and Co2+ modified-DNA crystals

We studied the physical characteristics of modified-DNA (M-DNA) double crossover crystals fabricated via substrate-assisted growth with various concentrations of four different divalent metallic ions, Cu(2+), Ni(2+), Zn(2+), and Co(2+). Atomic force microscopy (AFM) was used to test the stability of the M-DNA crystals with different metal ion concentrations. The AFM images show that M-DNA crystals formed without deformation at up to the critical concentrations of 6 mM of [Cu(2+)], 1.5 mM of [Ni(2+)], 1 mM of [Zn(2+)], and 1 mM of [Co(2+)]. Above these critical concentrations, the M-DNA crystals exhibited deformed, amorphous structures. Raman spectroscopy was then used to identify the preference of the metal ion coordinate sites. The intensities of the Raman bands gradually decreased as the concentration of the metal ions increased, and when the metal ion concentrations increased beyond the critical values, the Raman band of the amorphous M-DNA was significantly suppressed. The metal ions had a preferential binding order in the DNA molecules with G-C and A-T base pairs followed by the phosphate backbone. A two-probe station was used to measure the electrical current-voltage properties of the crystals which indicated that the maximum currents of the M-DNA complexes could be achieved at around the critical concentration of each ion. We expect that the functionalized ion-doped M-DNA crystals will allow for efficient devices and sensors to be fabricated in the near future.

Chemical and Physical Characteristics of Doxorubicin Hydrochloride Drug-Doped Salmon DNA Thin Films

Double-stranded salmon DNA (SDNA) was doped with doxorubicin hydrochloride drug molecules (DOX) to determine the binding between DOX and SDNA, and DOX optimum doping concentration in SDNA. SDNA thin films were prepared with various concentrations of DOX by drop-casting on oxygen plasma treated glass and quartz substrates. Fourier transform infrared (FTIR) spectroscopy was employed to investigate the binding sites for DOX in SDNA, and electrical and photoluminescence (PL) analyses were used to determine the optimum doping concentration of DOX. The FTIR spectra showed that up to a concentration of 30u2009μM of DOX, there was a tendency for binding with a periodic orientation via intercalation between nucleosides. The current and PL intensity increased as the DOX concentration increased up to 30u2009μM, and then as the concentration of DOX further increased, we observed a decrease in current as well as PL quenching. Finally, the optical band gap and second band onset of the transmittance spectra were analyzed to further verify the DOX binding and optimum doping concentration into SDNA thin films as a function of the DOX concentration.

Low-temperature growth of layered molybdenum disulphide with controlled clusters

Layered molybdenum disulphide was grown at a low-temperature of 350u2009°C using chemical vapour deposition by elaborately controlling the cluster size. The molybdenum disulphide grown under various sulphur-reaction-gas to molybdenum-precursor partial-pressure ratios were examined. Using spectroscopy and microscopy, the effect of the cluster size on the layered growth was investigated in terms of the morphology, grain size, and impurity incorporation. Triangular single-crystal domains were grown at an optimized sulphur-reaction-gas to molybdenum-precursor partial-pressure ratio. Furthermore, it is proved that the nucleation sites on the silicon-dioxide substrate were related with the grain size. A polycrystalline monolayer with the 100-nm grain size was grown on a nucleation site confined substrate by high-vacuum annealing. In addition, a field-effect transistor was fabricated with a MoS2 monolayer and exhibited a mobility and on/off ratio of 0.15u2009cm2 V−1 s−1 and 105, respectively.

Combining protein-shelled platinum nanoparticles with graphene to build a bionanohybrid capacitor.

The electronic properties of biomolecules and their hybrids with inorganic materials can be utilized for the fabrication of nanoelectronic devices. Here, we report the charge transport behavior of protein-shelled inorganic nanoparticles combined with graphene and demonstrate their possible application as a bionanohybrid capacitor. The conductivity of PepA, a bacterial aminopeptidase used as a protein shell (PS), and the platinum nanoparticles (PtNPs) encapsulated by PepA was measured using a field effect transistor (FET) and a graphene-based FET (GFET). Furthermore, we confirmed that the electronic properties of PepA-PtNPs were controlled by varying the size of the PtNPs. The use of two poly(methyl methacrylate) (PMMA)-coated graphene layers separated by PepA-PtNPs enabled us to build a bionanohybrid capacitor with tunable properties. The combination of bioinorganic nanohybrids with graphene is regarded as the cornerstone for developing flexible and biocompatible bionanoelectronic devices that can be integrated into bioelectric circuits for biomedical purposes.

A Conductive Copolymer Based on Graphene Oxide and Poly (amidoxime-pyrrole) for Adsorption of Uranium (VI)

A novel conducting copolymer based on amidoxime groups, polypyrrole and graphene oxide was synthesized by in situ copolymerization by usin g two monomers. The monomer, amidoxime-pyrrole, was synthesized by amidoximation of 1-(2-cyanoethyl) pyrrole. The other monomer, GO-pyrrole, was prepared via esterification between –COOH of GO and –NH2 of 1-(3-aminopropyl) pyrrole. The conductive ability of the copolymer was based on conductive π-conjugated system of polypyrrole backbone. The copolymer was able to be used as an effective sorption material for the preconcentration and recovery of uranium. The maximum of adsorption capacity for uranyl ion is as high as 149.57mg/g.

Conditioning of graphene surface by CO2 cluster jet

The reduction of resistance and surface roughness obtained by CO2 cluster jet were up to 81% and 42.3% compared with pristine graphene. The shifts in Raman spectra also implied chemical doping and “mono-layerization”. Thus, CO2 cluster jet has the potential for planarization, cleaning and flattening of the graphene.

LIGHT-SENSITIVE SILICON NANOWIRE ARRAY FIELD EFFECT TRANSISTOR FOR GLUCOSE DETECTION

We report on the sensitive detection of glucose using silicon nanowire array field-effect-transistor (SiNW-FET) upon illumination. The uniformly distributed and size-controlled SiNWs were fabricated by top-down approach. The fabricated SiNW-FET device was evaluated for detection of glucose in the range of 100–900 mg/dL. The SiNW-FET shows enhanced sensitivity of 0.988 ± 0.030 nA (mg/dl)-1 upon illumination at 480 nm light as compared to without illumination as 0.486 ± 0.014 nA (mg/dL)-1. The presented SiNW-FET device is fast, stable and sensitive to light as well as to bio analyte, and hence can be utilized as sensitive biological sensing platform.