Soonjoo Seo

Ambipolar rubrene thin film transistors

We report ambipolar field-effect transistors fabricated from rubrene thin films on SiO2∕Si substrates. The mobilities of both holes and electrons were extremely low, ranging from 2.2×10−6to8.0×10−6cm2∕Vs, due to disorder in the films. Rubrene forms three-dimensional circular islands even at extremely low coverages and x-ray diffraction observations suggest that the film is amorphous. The formation of the conducting channel of the transistor follows the geometric percolation of rubrene islands.

Channel formation in single-monolayer pentacene thin film transistors

The geometrical arrangement of single-molecule-high islands and the contact between them have large roles in determining the electrical properties of field effect transistors (FETs) based on monolayer-scale pentacene thin films. As the pentacene coverage increases through the submonolayer regime there is a percolation transition where islands come into contact and a simultaneous rapid onset of current. At coverages just above the percolation threshold, the electrical properties vary with geometrical changes in the contacts between the pentacene islands. At higher coverages, the FET mobility is much lower than the mobility measured by the van der Pauw method because of high contact resistances in monolayer-scale pentacene film devices. An increase in the van der Pauw mobility of holes as a function of pentacene coverage shows that second layer islands take part in charge transport.

Orientation of pentacene molecules on SiO2: From a monolayer to the bulk

Near edge x-ray absorption fine structure (NEXAFS) spectroscopy is used to study the orientation of pentacene molecules within thin films on SiO2 for thicknesses ranging from monolayers to the bulk (150 nm). The spectra exhibit a strong polarization dependence of the pi* orbitals for all films, which indicates that the pentacene molecules are highly oriented. At all film thicknesses the orientation varies with the rate at which pentacene molecules are deposited, with faster rates favoring a thin film phase with different tilt angles and slower rates leading to a more bulklike orientation. Our NEXAFS results extend previous structural observations to the monolayer regime and to lower deposition rates. The NEXAFS results match crystallographic data if a finite distribution of the molecular orientations is included. Damage to the molecules by hot electrons from soft x-ray irradiation eliminates the splitting between nonequivalent pi* orbitals, indicating a breakup of the pentacene molecule.

Advanced nanoporous TiO2 photocatalysts by hydrogen plasma for efficient solar-light photocatalytic application

We report an effect involving hydrogen (H2)-plasma-treated nanoporous TiO2(H-TiO2) photocatalysts that improve photocatalytic performance under solar-light illumination. H-TiO2 photocatalysts were prepared by application of hydrogen plasma of assynthesized TiO2(a-TiO2) without annealing process. Compared with the a-TiO2, the H-TiO2 exhibited high anatase/brookite bicrystallinity and a porous structure. Our study demonstrated that H2 plasma is a simple strategy to fabricate H-TiO2 covering a large surface area that offers many active sites for the extension of the adsorption spectra from ultraviolet (UV) to visible range. Notably, the H-TiO2 showed strong ·OH free-radical generation on the TiO2 surface under both UV- and visible-light irradiation with a large responsive surface area, which enhanced photocatalytic efficiency. Under solar-light irradiation, the optimized H-TiO2 120(H2-plasma treatment time: 120 min) photocatalysts showed unprecedentedly excellent removal capability for phenol (Ph), reactive black 5(RB 5), rhodamine B (Rho B) and methylene blue (MB) — approximately four-times higher than those of the other photocatalysts (a-TiO2 and P25) — resulting in complete purification of the water. Such well-purified water (>90%) can utilize culturing of cervical cancer cells (HeLa), breast cancer cells (MCF-7), and keratinocyte cells (HaCaT) while showing minimal cytotoxicity. Significantly, H-TiO2 photocatalysts can be mass-produced and easily processed at room temperature. We believe this novel method can find important environmental and biomedical applications.

Triangular Black Phosphorus Atomic Layers by Liquid Exfoliation

Few-layer black phosphorus (BP) is the most promising material among the two-dimensional materials due to its layered structure and the excellent semiconductor properties. Currently, thin BP atomic layers are obtained mostly by mechanical exfoliation of bulk BP, which limits applications in thin-film based electronics due to a scaling process. Here we report highly crystalline few-layer black phosphorus thin films produced by liquid exfoliation. We demonstrate that the liquid-exfoliated BP forms a triangular crystalline structure on SiO2/Si (001) and amorphous carbon. The highly crystalline BP layers are faceted with a preferred orientation of the (010) plane on the sharp edge, which is an energetically most favorable facet according to the density functional theory calculations. Our results can be useful in understanding the triangular BP structure for large-area applications in electronic devices using two-dimensional materials. The sensitivity and selectivity of liquid-exfoliated BP to gas vapor demonstrate great potential for practical applications as sensors.

Molecular structure of extended defects in monolayer-scale pentacene thin films

The growth of pentacene thin films for applications in thin-film transistors and other organic electronic devices results in a variety of extended structural defects including dislocations, grain boundaries, and stacking faults. We have used scanning tunneling microscopy (STM) to probe the molecular-scale structure of grain boundaries and stacking faults in a pentacene thin film on a Si (001) surface modified with styrene. Styrene/Si (001) substrates produce pentacene films that are structurally similar to those grown on insulating substrates, but which are sufficiently smooth and conductive for STM studies. STM images show two types of grain boundaries: in-plane high-angle tilt grain boundaries at the junctions between pentacene islands, and twist boundaries between molecular layers. Segments of the tilt grain boundaries are faceted along low-energy crystallographic directions. Stacking faults are found in the plane of individual pentacene grains. Two rows of molecules near the stacking fault are shifted...

Efficient harvesting of wet blue-green microalgal biomass by two-aminoclay [AC]-mixture systems

Blue-green microalgal blooms have been caused concerns about environmental problems and human-health dangers. For removal of such cyanobacteria, many mechanical and chemical treatments have been trialled. Among various technologies, the flocculation-based harvesting (precipitation) method can be an alternative if the problem of the low yield of recovered biomass at low concentrations of cyanobacteria is solved. In the present study, it was utilized mixtures of magnesium aminoclay [MgAC] and cerium aminoclay [CeAC] with different particle sizes to harvest cyanobacteria feedstocks with ∼100% efficiency within 1h by ten-fold lower loading of ACs compared with single treatments of [MgAC] or [CeAC]. This success was owed to the compact networks of the different-sized-ACs mixture for efficient bridging between microalgal cells. In order to determine the usage potential of biomass harvested with AC, the mass was heat treated under the reduction condition. This system is expected to be profitably utilizable in adsorbents and catalysts.

Molecular-scale structural distortion near vacancies in pentacene

Molecular vacancies form in both of the crystallographic basis sites of thin pentacene crystals. Features in scanning tunneling microscopy images of these crystals correspond to the exposed terminal atoms of molecules. The (001) and (001¯) surfaces of pentacene are distinguishable, which allows for the identification of the absolute orientation of crystals and for the unambiguous assignment of the position of molecules relative to each vacancy. For vacancies in each molecular basis site of the pentacene (001) surface, the image feature associated with one molecular nearest neighbor is displaced by significantly more than other molecules.

Molecular-Scale Structure of Pentacene Interfaces with Si (111)

The morphology and crystal structure of the first few molecular layers of organic semiconductor thin films at organic-inorganic interfaces are important from both electronic and structural perspectives. The first upright layer of pentacene on Si (111) forms on top of a disordered layer of strongly bonded pentacene molecules in a structure similar to the pentacene monolayers formed on insulators. We describe a high-resolution structural study of this crystalline phase of pentacene using low-temperature scanning tunneling microscopy (STM). The arrangement of molecules in these layers observed with STM agrees the results of with structural studies using scattering techniques. The imaging conditions and sample preparation techniques necessary to achieve molecular resolution can be adapted to subsequent STM and scanning tunneling spectroscopy experiments probing individual structural defects including vacancies, dislocations and grain boundaries within and between islands.