1,136 research outputs found
Excitons and high-order optical transitions in individual carbon nanotubes
We examine the excitonic nature of high-lying optical transitions in
single-walled carbon nanotubes by means of Rayleigh scattering spectroscopy. A
careful analysis of the principal transitions of individual semiconducting and
metallic nanotubes reveals that in both cases the lineshape is consistent with
an excitonic model, but not one of free-carriers. For semiconducting species,
side-bands are observed at ~200 meV above the third and fourth optical
transitions. These features are ascribed to exciton-phonon bound states. Such
side-bands are not apparent for metallic nanotubes,as expected from the reduced
strength of excitonic interactions in these systems
Probing the Intrinsic Properties of Exfoliated Graphene: Raman Spectroscopy of Free-Standing Monolayers
The properties of pristine, free-standing graphene monolayers prepared by
mechanical exfoliation of graphite are investigated. The graphene monolayers,
suspended over open trenches, are examined by means of spatially resolved Raman
spectroscopy of the G-, D-, and 2D-phonon modes. The G-mode phonons exhibit
reduced energies (1580 cm-1) and increased widths (14 cm-1) compared to the
response of graphene monolayers supported on the SiO2 covered substrate. From
analysis of the G-mode Raman spectra, we deduce that the free-standing graphene
monolayers are essentially undoped, with an upper bound of 2x10^11 cm-2 for the
residual carrier concentration. On the supported regions, significantly higher
and spatially inhomogeneous doping is observed. The free-standing graphene
monolayers show little local disorder, based on the very weak Raman D-mode
response. The two-phonon 2D mode of the free-standing graphene monolayers is
downshifted in frequency compared to that of the supported region of the
samples and exhibits a narrowed, positively skewed line shape
Graphene Oxidation: Thickness Dependent Etching and Strong Chemical Doping
Patterned graphene shows substantial potential for applications in future
molecular-scale integrated electronics. Environmental effects are a critical
issue in a single layer material where every atom is on the surface. Especially
intriguing is the variety of rich chemical interactions shown by molecular
oxygen with aromatic molecules. We find that O2 etching kinetics vary strongly
with the number of graphene layers in the sample. Three-layer-thick samples
show etching similar to bulk natural graphite. Single-layer graphene reacts
faster and shows random etch pits in contrast to natural graphite where
nucleation occurs at point defects. In addition, basal plane oxygen species
strongly hole dope graphene, with a Fermi level shift of ~0.5 eV. These oxygen
species partially desorb in an Ar gas flow, or under irradiation by far UV
light, and readsorb again in an O2 atmosphere at room temperature. This
strongly doped graphene is very different than graphene oxide made by mineral
acid attack.Comment: 15 pages, 5 figure
Two wheeled lunar dumptruck
The design of a two wheel bulk material transport vehicle is described in detail. The design consists of a modified cylindrical bowl, two independently controlled direct drive motors, and two deformable wheels. The bowl has a carrying capacity of 2.8 m (100 ft) and is constructed of aluminum. The low speed, high HP motors are directly connected to the wheels, thus yielding only two moving parts. The wheels, specifically designed for lunar applications, utilize the chevron tread pattern for optimum traction. The vehicle is maneuvered by varying the relative angular velocities of the wheels. The bulk material being transported is unloaded by utilizing the motors to oscillate the bowl back and forth to a height at which dumping is achieved. The analytical models were tested using a scaled prototype of the lunar transport vehicle. The experimental data correlated well with theoretical predictions. Thus, the design established provides a feasible alternative for the handling of bulk material on the moon
LETTERS Reversible Oxidation Effect in Raman Scattering from Metallic Single-Wall Carbon Nanotubes
Raman scattering from individual single-wall carbon nanotube (SWNT) bundles was measured using confocal optical microscopy with 632 nm laser excitation. The Raman scattering from metallic SWNTs was found to depend sensitively on adsorbed oxidizing molecules. Tangential mode Raman lines of HNO 3 -treated SWNTs exhibited different line shapes from those of H 2 SO 4 /H 2 O 2 -treated SWNTs. However, the line shapes became identical after high power laser irradiation, which heats the bundle to ∼750 K based on measurement of the breathing mode Stokes to anti-Stokes Raman intensity ratio. Thermal annealing of both samples at 873 K caused the same change in Raman spectra as with laser irradiation, which is attributed to degassing of doping adsorbates. A mechanism of charge transfer between carbon nanotubes and adsorbate molecules is proposed to explain the large change in Raman scattering from metallic SWNTs upon chemical doping and degassing. Raman scattering from degassed SWNT bundles was found to show a linear dependence on excitation intensity, suggesting that Raman cross sections do not change with temperature in the range 300-750 K
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