Characterization of temperature-dependent carrier transport in disordered indium-tin-oxide/poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)/polyfluorene/Ca/Al polymer structures

The temperature-dependent electrical characteristics of polyfluorene-based polymer structures over a temperature range from 200 to 300 K are systematically investigated in this study. Initially, using the definitions of the Berthelot-type model, it is found that the sample exhibits a higher Berthelot-type temperature T_B with high driving voltage, indicating that carrier transport in a disordered system manifests Berthelot-type behaviors. The ideal current density-voltage curve for the polymer structures given the carrier transmit mechanism is further elucidated by taking into account the ohmic conduction, trap charge limited current, and Mott and Gurney model of space charge limited current. The proposed procedure is simple and can be used to characterize the material with reasonable accuracy. We also study the density of the traps H_t, and the characteristic energy of the distribution E_t to better understand the carrier-transport process in organic materials and structures.     

Fabrication of monolayer of polymer/nanospheres hybrid at a water-air interface

A new type of polymer-assisted self-assembly of nanospheres at a water-air interface was uncovered. By adding merely 1-3 ppm of polyethylene oxide in the water, the polystyrene nanospheres, applicable to diameters ranging from 100 nm to 1 μm, were found to gradually move closer to each other and eventually form a close-packed structure confirmed from its diffraction pattern. As it turns out, polyethylene oxides are adsorbed onto the surface of polystyrene nanospheres, giving rise to the effective screening of coulomb repulsive force between nanospheres followed by the onset of polymer-bridging effect as demonstrated from the strong suppression of Brownian motion. The resulting monolayer of close-packed polymer/nanospheres hybrid at the water-air interface with area size more than 1 cm(2) are robust and can be transferred to a substrate of any kind without serious breaking due to surface tension tearing. Our finding may provide a further extension to the scope of nanosphere lithography technique.     

Electronic and optical properties of monolayer and bilayer graphene

The electronic and optical properties of monolayer and bilayer graphene are investigated to verify the effects of interlayer interactions and external magnetic field. Monolayer graphene exhibits linear bands in the low-energy region. Then the interlayer interactions in bilayers change these bands into two pairs of parabolic bands, where the lower pair is slightly overlapped and the occupied states are asymmetric with respect to the unoccupied ones. The characteristics of zero-field electronic structures are directly reflected in the Landau levels. In monolayer and bilayer graphene, these levels can be classified into one and two groups, respectively. With respect to the optical transitions between the Landau levels, bilayer graphene possesses much richer spectral features in comparison with monolayers, such as four kinds of absorption channels and double-peaked absorption lines. The explicit wave functions can further elucidate the frequency-dependent absorption rates and the complex optical selection rules. These numerical calculations would be useful in identifying the optical measurements on graphene layers.     

Spray pyrolysis deposition of polycrystalline magnesia films and their use as buffer layers in Bi(Pb)-Sr-Ca-Cu-O/MgO/Al2O3 (or glass ceramics) structures

The deposition of MgO films on Al₂O₃ and glass ceramic substrates by spray pyrolysis of a water-ethanol magnesium nitrate precursor solution has been studied. Dense polycrystalline films have been obtained by repeated pyrolysis at 300–350 °C followed by annealing of the deposit in air at 970 °C. It has been established that the finest grains obtained under these experimental conditions correspond to the films deposited on glass ceramic substrates. It has been shown that the MgO films can be useful buffer layers preventing the interaction between the above substrates and the BiSr-Ca-Cu-O films deposited on them by spray pyrolysis of nitrates.     

Deposition of polymer bilayer configuration by pulsed laser ablation and its use for study of polymer-polymer interface

Thin films of polyphenylene sulphide (PPS) and polyethylene (PE) polymers have been deposited in a bilayer configuration using pulsed excimer laser ablation. Such bilayer specimens have been annealed at different temperatures, up to a maximum of 120°C, and for different time intervals, up to a maximum of 110 min, to investigate the evolution of the interface. By employing the technique of spectroscopic ellipsometry, the nature and the degree of thermally induced polymeric transport across the interface are brought out.     

Dielectric/metal/dielectric structures using copper as metal and MoO3 as dielectric for use as transparent electrode

Transparent conductive oxide/metal/oxide, where the oxide is MoO₃ and the metal is Cu, is realized and characterized. The films are deposited by simple joule effect. It is shown that relatively thick Cu films are necessary for achieving conductive structures, what implies a weak transmission of the light. Such large thicknesses are necessary because Cu diffuses strongly into the MoO₃ films. We show that the Cu diffusion can be strongly limited by sandwiching the Cu layer between two Al ultra-thin films (1.4 nm). The best structures are glass/MoO₃ (20 nm)/Al (1.4 nm)/Cu (18 nm)/Al (1.4 nm)/MoO₃ (35 nm). They exhibit a transmission of 70% at 590 nm and a resistivity of 5.0 · 10^− 4 Ω cm. A first attempt shows that such structures can be used as anode in organic photovoltaic cells.     

Characterization of interface states at Au/SnO2/n-Si (MOS) structures

The purpose of this paper is to characterize the interface states in Au/SnO₂/n-Si (MOS) structures. The characteristic parameters of the interface states are derived from capacitance-voltage (C-V) and conductance-voltage (G/ω-V) measurements as a function of frequency. The C-V and G/ω-V measurements have been carried out in the frequency range of 1 kHz to 1 MHz at room temperature. At each frequency, the measured capacitance and conductance decrease with increasing frequency due to a continuous distribution of the interface states. The frequency dispersion in capacitance and conductance can be interpreted in terms of the interface state density (N_ss) and series resistance (R_s). Especially at low frequencies, the interface states can follow the ac signal and yield an excess capacitance. Due to a continuous density distribution of interface states, the C and G/ω values decrease in depletion region with increasing frequencies. At high frequencies, the effect of series resistance on the capacitance is found appreciable due to the interface state capacitance decreasing with increasing frequency. Experimental results show that the locations of interface states between SnO₂/Si and series resistance have a significant effect on electrical characteristics of MOS structures.     

The chemical reactivity of graphite fluoride in conjunction with its use as a solid lubricant

Interpretation of differential scanning calorimetry (DSC) results suggest that on heating tin/graphite fluoride, cadmium/graphite fluoride and indium/graphite fluoride mixtures to 773 K, chemical reactions occur. Examination of the reaction products from these reactions by X-ray photoelectron spectroscopy (XPS) clearly shows the presence of metallic fluorides. These fluorides are also formed on evaporation of tin, cadmium and indium onto the clean polymer surface. Graphite fluoride flims rubbed on stainless steel, nickel and aluminium counterfaces also form metal fluorides at the interface suggesting a different interpretation of the mode of failure of the lubricant film of this material.     

Synthesis of Ag(2) S-Ag nanoprisms and their use as DNA hybridization probes

A simple synthetic route to prepare Ag(2) S-Ag nanoprisms consists of the facile addition of Na(2) S to a solution of triangular Ag nanoprisms. The resulting Ag(2) S-Ag nanoparticles are more stable in solution than the original Ag nanoprisms, and two surface plasmon resonance (SPR) bands of the original Ag nanoprisms still remain. In addition, the SPR bands of the Ag(2) S-Ag nanoprisms are tunable over a wide range. The Ag(2) S-Ag nanoprisms can be directly bioconjugated via well-established stable Ag(2) S surface chemistry with readily available sulfur coupling agents. The nanoprisms are used in the hybridization of functionalized oligonucleotides, and show promise as probes for future biosensing applications.     

Patterned monolayer/polymer films for analysis of dilute or salt-contaminated protein samples by MALDI-MS

This paper describes a surface science/mass spectrometry effort to develop and characterize a patterned gold surface that serves as a MALDI sample platform capable of concentrating and purifying proteins. Using microcontact printing, small (200-microm diameter) hydrophilic spots of bare gold or chemically anchored poly(acrylic acid) (PAA) are patterned at 5-mm intervals in a hydrophobic field consisting of a self-assembled monolayer of hexadecanethiol. Building on recent innovations by others, the small hydrophilic spots concentrate the sample to achieve good reproducibility and high sensitivity in the MALDI signal. One of the key features in this work is the combination of the high density of carboxylate groups in PAA with a small spot size to afford both concentration and purification of proteins via ionic interactions. This translates into detection limits for salt-contaminated proteins that are 20-100 times lower (low femtomole) than those reported for previous polymer- or monolayer-modified MALDI probes (using proteins in the 3-15-kDa range). Reflectance FT-IR spectroscopy and ellipsometry were used to determine the amount of protein adsorbed to a PAA-modified sample plate as a function of pH and salt concentration. Amide absorbances in IR spectra correlate well with MALDI-MS signals measured after addition of 2,5-dihydroxybenzoic acid as a matrix.     

Characterization of tin(II) sulfide defects/vacancies and correlation with their photocurrent

The presence of defects/vacancies in nanomaterials influences the electronic structure of materials, and thus, it is necessary to study the correlation between the optoelectronic properties of a nanomaterial and its defects/vacancies. Herein, we report a facile solvothermal route to synthesize three-dimensional (3D) SnS nanostructures formed by {131} faceted nanosheet assembly. The 3D SnS nanostructures were calcined at temperatures of 350, 400, and 450 °C and used as counter electrodes, before their photocurrent properties were investigated. First principle computation revealed the photocurrent properties depend on the defect/vacancy concentration within the samples. It is very interesting that characterization with positron annihilation spectrometry confirmed that the density of defects/vacancies increased with the calcination temperature, and a maximum photocurrent was realized after treatment at 400 °C. Further, the defect/vacancy density decreased when the calcination temperature reached 450 °C as the higher calcination temperature enlarged the mesopores and densified the pore walls, which led to a lower photocurrent value at 450 °C than at 400 °C.

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Characterization of perylene diimide dye self-assemblies and their use as templates for the synthesis of hybrid and supermicroporous nanotubules

The self-organizing structures formed by a water-soluble perylene diimide dye (PDI) have been studied by several experimental techniques as potential templates for the preparation of hybrid nanomaterials. The dye forms chromonic-nematic and hexagonal liquid crystals in water. The aggregates in liquid crystals consist of one-molecule-wide stacks. From the changes in the solution proton NMR chemical shifts with concentration, it appears that adjacent molecules are twisted. There is significant broadening of the aromatic resonances at higher concentrations, arising from nonmotionally averaged dipole-dipole coupling between adjacent aromatic hydrogens. This is attributed to slow overall rotation of the aggregates in solution, suggesting that they grow up to several tens of nanometers. Dye aggregates serve as templates for the formation of silica tubules (1-5 μm length, average diameter ≈300 nm), with aligned and very thin (1-2 nm) dye nanostripes embedded in the walls. The silica tubes precipitated from solution are formed by the cooperative interaction between PDI and silica species during the sol-gel reaction. Upon calcination, silica nanotubules with supermicroporous walls are obtained. In comparison with conventional surfactant systems, the use of π-π stacked chromonic aggregates brings new possibilities for the templated fabrication of pores with sizes below the mesoporous range. Materials could find applications in photovoltaics as well as in shape selective catalysis and adsorption.