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Atomically thin molybdenum disulfide (MoS2) films were synthesized on a SiO2/Si substrate by metal-organic chemical vapor deposition (MOCVD). Raman spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy studies reveal the double-atomic-layer structure and the surface element composition of the MOCVD-grown MoS2 films. The photoluminescence measurement demonstrates a strong emission peak with a bandgap of 685.1 nm, attributed to highly efficient radiative transition at the double atomic layer. The contact resistance between the doubleatomic-layer MoS2 film and metal electrode was measured using the transmission-line modeling method. A Ti/Au electrode forms an ohmic contact with the double-atomic-layer MOCVD-grown MoS2 film, exhibiting a resistivity of 100 kΩ. The field-effect transistor based on the double-atomiclayer MoS2 film exhibits an electron mobility of 1.3×10−4 cm2/V·s and an on/off ratio of 6.5×102 at room temperature.

An amphiphillic fullerene pentaphenol derivative, C60(4-HOC6H4)5H, in an aprotic solvent N-methyl-2-pyrrolidone (NMP), spontaneously self-assembles to a hitherto unknown cheese stick-like (CS) structure. This fascinating structure is observed only for C60(4-HOC6H4)5H and only in dry NMP solvent. The reason for such unique self-assembly behavior is ascribed to solvating power typical of NMP. The CS structure is observed in a narrow concentration range of the solution. This indicates that there exists between the solute and the solvent an optimal interaction condition for CS to remain stable.

A series of Co (5-30 wt%) based SiC supported catalysts were prepared by impregnation method and investigated for FTS reaction. The FTS reaction was carried out in a fixed bed reactor system with the H2/CO molar ratio of 2, reaction temperature of 230 degrees C and reaction pressure of 20 bar for 120 h. All catalysts were characterized by N2 physisorption, XRD, TPR, SEM and TEM techniques. It was found that 15 wt% Co/SiC catalyst showed better catalytic performance with high selectivity of C(5+) hydrocarbons than the other catalysts. The results, suggest that the catalytic performance of the catalysts depends on average pore size of support and surface density of cobalt, metal and support interactions.

Poly(vinyl pyrrolidone) (PVP)-stabilized silver nanoparticles (NPs) were used as a new nanocomposite resist for electron beam lithography. A nanocomposite resist prepared by reducing silver nitrate in an alcoholic PVP solution was patterned by using a scanning electron microscope equipped with a nanometer pattern generation system. Well-defined negative tone patterns with a good sensitivity of 200 microC/cm2 and a contrast of 2.83 were obtained using the prepared nanocomposite resist. In addition, the changes in the morphology and structure of the resist patterns with a thermal treatment temperature were investigated by a FE-SEM with an EDX. The results revealed that the patterns of Ag NPs were formed through sintering the formed resist patterns at above 300 degrees C.

The effect of solvent compositions on the micellization behaviors of amphiphilic poly(n-hexyl isocyanate)-b-poly(2-vinylpyridine)-b-poly(n-hexyl isocyanate) (PHIC-b-P2VP-b-PHIC) rod-coil-rod triblock copolymer was studied. In absolute methanol the block copolymer formed hollow spherical micelles. These micelles transformed into giant-tubes by simply changing the solvent composition. With 20% THF in CH3OH hollow spheres got interconnected and formed species that are precursors of the giant tubes. When the composition of THF reached 50–70%, long giant tubes are formed. Further increasing THF content in the mixed solvent, fragmentation of the wall of the tubes was observed. In absolute THF, which is the common solvent for both the blocks, the usual phase separation occurred. TEM image of the giant tubes stained with iodine showed that the core of the tubes is made from PHIC rod block.

The polystyrene-poly(arylene ether sulfone)-polystyrene (PS-PAES-PS) coil-semirod-coil triblock copolymer was synthesized by the condensation reaction of PS-COCl and H2N-PAES-NH2 telechelic polymers. The reaction was facile characterized by high yields with a perfect control over the block lengths. Following a known reaction protocol it was possible to selectively sulfonate the PS block of the triblock copolymer that led to the sulfonated copolymer sPS-PAES-sPS. Studies on its proton conductivity and methanol permeability were carried out to evaluate its use as the proton exchange membrane in direct methanol fuel cells. Proton conductivity of the membranes was increased depending on the sulfonic acid group content in the sulfonated polymer. The membranes exhibited good dimensional and thermal stability, and low methanol permeability compared to Nafion 117.