Multiwalled carbon nanotubes mass-produced by dc arc discharge in He–H2 gas mixture

Uniform cathode deposits (longer than 15 mm), containing multiwalled carbon nanotubes (MWNTs) inside, were produced by dc arc discharge evaporation with a computer-controlled feeder of a pure-carbon electrode without a metal catalyst in a He–H₂ gas mixture. The purification of MWNTs was carried out to remove amorphous carbon and carbon nanoparticles. High-resolution transmission electron microscopy observations and Raman scattering studies show that the MWNTs possess a high crystallinity and a mean outermost diameter of ∼ ∼10 nm. It has been confirmed that the current density in the electron field emission from a purified MWNT mat can reach 77.92 mA/cm², indicating that the purified MWNTs are a promising candidate electron source in a super high-luminance light-source tube or a miniature X-ray source.     

WIDE RANGE DETECTOR USING PARABOLIC CYLINDRICAL MIRROR FOR THz APPLICATIONS

A new, wide-band, high-speed and high-sensitivity THz detector has been developed. The prototype detector consists of a parabolic cylindrical mirror, a long wire antenna and a Schottky barrier diode. Direct detection measurements have shown a stable sensitivity of 150 ± 50 V/W for 1–2 THz without any adjustments. The long wire antenna was fixed at the focus of parabolic cylindrical mirror then it has been realized less operation steps, easy coupling to the external THz signals and a dramatic enhancement in the practicality of this system. The optically polished mirror and frosted surface one showed comparable sensitivities, thus easy polishing and less cost mirror fabrication can be applied for this system. The radiation pattern showed a maximum radiation angle of approximately 23° with its dominant main lobe, which was attributed to the wire antenna character and confirmed good agreements with classical antenna theory.     

Synthesis of Al–Cr decagonal quasicrystal nanoparticles and their temperature of phase transformation to stable crystal phase

The synthesis of Al–Cr single quasicrystal (QC) nanoparticles of the decagonal phase was achieved by introducing an advanced gas flow evaporation method. By obtaining successive electron diffraction patterns for single-QC nanoparticles, the phase transformation temperature of a single-QC nanoparticle was determined to be 700 °C. It was also determined that part of the QC nanoparticle decomposed into hex-Al₈Cr₅ and Al during the phase transformation. Since the grain growth did not occur during the phase transformation in the present experiment, the inherent phase transformation temperature could be measured.     

Simultaneous observation of CO isotopomer absorption by broadband difference-frequency generation using a direct-bonded quasi-phase-matched LiNbO3 waveguide

Rovibration absorption lines both of 12CO and 13CO are observed simultaneously with the output of a 2 microm broadband difference frequency generated in a direct-bonded quasi-phase-matched LiNbO3 waveguide, which is a 50 mm device with a single quasi-phase-matching period that is operated at a constant temperature. The wavelength conversion efficiency and the difference-frequency generation bandwidth reach 100%/W and 100 nm, respectively. The idler output bandwidth in the 2 microm region is obtained by group-velocity matching or phase-mismatch minimization when a 0.94 microm pump laser diode and a 1.55 microm tunable signal source are used.     

Strong resonance enhancement of a single harmonic generated in the extreme ultraviolet range

We report the demonstration of strong resonance enhancement of a single high-order harmonic in the extreme ultraviolet (XUV) region generated from the interaction of a femtosecond pulse with low-ionized In ablation. A strong 13th harmonic (61.2 nm) of Ti:sapphire laser radiation with output intensity almost two orders of magnitude higher than neighboring harmonics was observed in these studies. The high conversion efficiency of the 13th harmonic (8 x 10(-5)) is attributed to multiple collisions of electron trajectories with the origin due to multiphoton resonance with the In ion.     

Quarkonia at Finite T: An Approach Based On QCD Sum Rules and the Maximum Entropy Method

Quarkonium spectral functions at finite temperature are studied, making use of a recently developed method of analyzing QCD sum rules by the maximum entropy method. This approach enables us to directly obtain the spectral function from the sum rules, without having to introduce any specific assumption about its functional form. QCD sum rules for heavy quarkonia incorporate finite temperature effects in form of changing values of the various gluonic condensates that appear in the operator product expansion. These changes depend on the energy density and pressure at finite temperature, which we extract from quenched lattice QCD calculations. As a result, it is found that the charmonium ground states of both S-wave and P-wave channels dissolve into the continuum already at temperatures around or slightly above the critical temperature T _c , while the bottomonium states are less influenced by temperature effects, surviving up to about 2.5 T _c or higher for S-wave and about 2.0 T _c for P-wave states.     

Controlling the orientation of polar molecules with combined electrostatic and pulsed,nonresonant laser fields

We demonstrate that molecules with a moderate permanent dipole moment can be oriented with combined electrostatic and pulsed, nonresonant laser fields. We use OCS molecules as a sample. The degree of orientation can be increased by increasing the magnitude of electrostatic field and the peak intensity of the laser field or by decreasing the rotational temperature of the molecules.     

Sliding acceleration of water droplets on a surface coated with fluoroalkylsilane and octadecyltrimethoxysilane

Both fluoroalkylsilane (FAS) and octadecyltrimethoxysilane (ODS) were coated on oxidized silicon wafers using soaking and CVD method. Smooth coatings with Ra values of less than 1 nm were attained. The slope of the sliding acceleration against the inverse of the droplet mass showed an inflection point. That point shifted to the direction of smaller droplets with decreasing FAS ratio to ODS. The water droplets’ length was increased when the sliding velocity was increased. Fluoroalkylsilane addition to ODS increases the interaction between water and the hydrophobic surface. Results showed that the sliding acceleration of a water droplet depends strongly on the surface ratio of these silanes.     

Dynamic hydrophobicity of water droplets on the line-patterned hydrophobic surfaces

Static and dynamic hydrophobicities of water droplet on a patterned surface prepared using fluoroalkylsilanes with different molecular chain lengths were investigated. Contact angles on the patterned surfaces well agreed with values predicted using Cassie’s theory. On the same line width ratio, total retention force was governed by the fluoroalkylsilane with slow-sliding acceleration. The total retention force decreased with the decreasing width ratio of silane with slow-sliding acceleration on the surface. These results imply that the sliding acceleration of water droplets on a hydrophobic surface depends both on chemical composition and patterning structure.     

The chemisorption of pentacene on Si(0 0 1)-2 × 1

Adsorption structures of the pentacene (C₂₂H₁₄) molecule on the clean Si(0 0 1)-2 × 1 surface were investigated by scanning tunneling microscopy (STM) in conjunction with density functional theory calculations and STM image simulations. The pentacene molecules were found to adsorb on four major sites and four minor sites. The adsorption structures of the pentacene molecules at the four major sites were determined by comparison between the experimental and the simulated STM images. Three out of the four theoretically identified adsorption structures are different from the previously proposed adsorption structures. They involve six to eight Si-C covalent chemical bonds. The adsorption energies of the major four structures are calculated to be in the range 67-128 kcal/mol. It was also found that the pentacene molecule hardly hopped on the surface when applying pulse bias voltages on the molecule, but was mostly decomposed.