1,253 research outputs found
A study to determine the optimum design of a photographic film for the lunar surface hand-held camera Final report
Design, and processing of photographic film for lunar surface hand operated camer
Spin-Orbit Coupling in Iridium-Based 5d Compounds Probed by X-ray Absorption Spectroscopy
We have performed x-ray absorption spectroscopy (XAS) measurements on a
series of Ir-based 5d transition metal compounds, including Ir, IrCl3, IrO2,
Na2IrO3, Sr2IrO4, and Y2Ir2O7. By comparing the intensity of the "white-line"
features observed at the Ir L2 and L3 absorption edges, it is possible to
extract valuable information about the strength of the spin-orbit coupling in
these systems. We observe remarkably large, non-statistical branching ratios in
all Ir compounds studied, with little or no dependence on chemical composition,
crystal structure, or electronic state. This result confirms the presence of
strong spin-orbit coupling effects in novel iridates such as Sr2IrO4, Na2IrO3,
and Y2Ir2O7, and suggests that even simple Ir-based compounds such as IrO2 and
IrCl3 may warrant further study. In contrast, XAS measurements on Re-based 5d
compounds, such as Re, ReO2, ReO3, and Ba2FeReO6, reveal statistical branching
ratios and negligible spin-orbit coupling effects.Comment: 9 pages, 4 figure
Long slit spectroscopy of NH2 in comets Halley, Wilson, and Nishikawa-Takamizawa-Tago
Long-slit spectra of comets Halley, Wilson and Nishikawa-Takamizawa-Tago were obtained with the 3.9 meter Anglo-Australian Telescope. Spectra of comets Halley and Wilson were obtained with the IPCS at a spectral resolution of 0.5 A and a spatial resolution of 10(exp 3) km. Spectra of comets Wilson and Nishikawa-Takamizawa-Tago were obtained with a CCD at a spectral resolution of 1.5 A and a spatial resolution of approximately 3 x 10(exp 3) km. Surface brightness profiles for NH2 were extracted from the long-slit spectra of each comet. The observed surface brightness profiles extend along the slit to approximately 6 x 10(exp 4) km from the nucleus in both sunward and tailward directions. By comparing surface distribution calculated from an appropriate coma model with observed surface brightness distributions, the photodissociation timescale of the parent molecule of NH2 can be inferred. The observed NH2 surface brightness profiles in all three comets compares well with a surface brightness profile calculated using the vectorial model, an NH3 photodissociation timescale of 7 x 10(exp 3) seconds, and an NH2 photodissociation timescale of 34,000 seconds
Electronic properties of silica nanowires
Thin nanowires of silicon oxide were studied by pseudopotential density
functional electronic structure calculations using the generalized gradient
approximation. Infinite linear and zigzag Si-O chains were investigated. A wire
composed of three-dimensional periodically repeated Si4O8 units was also
optimized, but this structure was found to be of limited stability. The
geometry, electronic structure, and Hirshfeld charges of these silicon oxide
nanowires were computed. The results show that the Si-O chain is metallic,
whereas the zigzag chain and the Si4O8 nanowire are insulators
Magneto-elastic coupling and unconventional magnetic ordering in triangular multiferroic AgCrS2
The temperature evolution of the crystal and magnetic structures of
ferroelectric sulfide AgCrS2 have been investigated by means of neutron
scattering. AgCrS2 undergoes at TN = 41.6 K a first-order phase transition,
from a paramagnetic rhombohedral R3m to an antiferromagnetic monoclinic
structure with a polar Cm space group. In addition to being ferroelectric below
TN, the low temperature phase of AgCrS2 exhibits an unconventional collinear
magnetic structure that can be described as double ferromagnetic stripes
coupled antiferromagnetically, with the magnetic moment of Cr+3 oriented along
b within the anisotropic triangular plane. The magnetic couplings stabilizing
this structure are discussed using inelastic neutron scattering results.
Ferroelectricity below TN in AgCrS2 can possibly be explained in terms of
atomic displacements at the magneto-elastic induced structural distortion.
These results contrast with the behavior of the parent frustrated
antiferromagnet and spin-driven ferroelectric AgCrO2
Simulation of thermal conductivity and heat transport in solids
Using molecular dynamics (MD) with classical interaction potentials we
present calculations of thermal conductivity and heat transport in crystals and
glasses. Inducing shock waves and heat pulses into the systems we study the
spreading of energy and temperature over the configurations. Phonon decay is
investigated by exciting single modes in the structures and monitoring the time
evolution of the amplitude using MD in a microcanonical ensemble. As examples,
crystalline and amorphous modifications of Selenium and are
considered.Comment: Revtex, 8 pages, 11 postscript figures, accepted for publication in
PR
Ab initio studies of phonon softening and high pressure phase transitions of alpha-quartz SiO2
Density functional perturbation theory calculations of alpha-quartz using
extended norm conserving pseudopotentials have been used to study the elastic
properties and phonon dispersion relations along various high symmetry
directions as a function of bulk, uniaxial and non-hydrostatic pressure. The
computed equation of state, elastic constants and phonon frequencies are found
to be in good agreement with available experimental data. A zone boundary (1/3,
1/3, 0) K-point phonon mode becomes soft for pressures above P=32 GPa. Around
the same pressure, studies of the Born stability criteria reveal that the
structure is mechanically unstable. The phonon and elastic softening are
related to the high pressure phase transitions and amorphization of quartz and
these studies suggest that the mean transition pressure is lowered under
non-hydrostatic conditions. Application of uniaxial pressure, results in a
post-quartz crystalline monoclinic C2 structural transition in the vicinity of
the K-point instability. This structure, intermediate between quartz and
stishovite has two-thirds of the silicon atoms in octahedral coordination while
the remaining silicon atoms remain tetrahedrally coordinated. This novel
monoclinic C2 polymorph of silica, which is found to be metastable under
ambient conditions, is possibly one of the several competing dense forms of
silica containing octahedrally coordinated silicon. The possible role of high
pressure ferroelastic phases in causing pressure induced amorphization in
silica are discussed.Comment: 17 pages, 8 figs., 8 Table
Mechanism of Thermal Atomic Layer Etch of W Metal Using Sequential Oxidation and Chlorination:A First-Principles Study
Thermal atomic layer etch (ALE) of W metal can be achieved by sequential self-limiting oxidation and chlorination reactions at elevated temperatures. In this paper, we analyze the reaction mechanisms of W ALE using the first-principles simulation. We show that oxidizing agents such as O2, O3, and N2O can be used to produce a WOx surface layer in the first step of an ALE process with ozone being the most reactive. While the oxidation pulse on clean W is very exergonic, our study suggests that runaway oxidation of W is not thermodynamically favorable. In the second ALE pulse, WCl6 and Cl2 remove the oxidized surface W atoms by the formation of volatile tungsten oxychloride (WxOyClz) species. In this pulse, each adsorbed WCl6 molecule was found to remove one surface W atom with a moderate energy cost. Our calculations further show that the desorption of the additional etch products is endothermic by up to 4.7 eV. Our findings are consistent with the high temperatures needed to produce ALE in experiments. In total, our quantum chemical calculations have identified the lowest energy pathways for ALE of tungsten metal along with the most likely etch products, and these findings may help guide the development of improved etch reagents
Excitonic effects in the optical properties of SiC sheet and nanotubes
The quasiparticle band structure and optical properties of single-walled
zigzag and armchair SiC nanotubes (SiC-NTs) as well as single SiC sheet are
investigated by ab initio many-body calculations using the GW and the GW plus
Bethe-Salpeter equation (GW+BSE) approaches, respectively. Significant GW
quasiparticle corrections of more than 1.0 eV to the Kohn-Sham band gaps from
the local density approximation (LDA) calculations are found. The GW
self-energy corrections transform the SiC sheet from a indirect LDA band gap to
a direct band gap material. Furthermore, the quasiparticle band gaps of SiC-NTs
with different chiralities behave very differently as a function of tube
diameter, and this can be attributed to the difference in the curvature-induced
orbital rehybridization between the different chiral nanotubes. The calculated
optical absorption spectra are dominated by discrete exciton peaks due to
exciton states with large binding energy up to 2.0 eV in the SiC sheet and
SiC-NTs. The formation of strongly bound excitons is attributed to the enhanced
electron-hole interaction in these low dimensional systems. Remarkably, the
excited electron amplitude of the exciton wavefunction is found to peak on the
Si atoms near the hole position (which is on the C site) in the zigzag SiC-NTs,
indicating a charge transfer from an anion (hole) to its neighboring cations by
photoexcitation. In contrast, this pronounced peak structure disappear in the
exciton wavefunction in the armchair SiC-NTs. Furthermore, in the armchair
SiC-NTs, the bound exciton wavefunctions are more localized and also strongly
cylindrically asymmetric
Interface energies of (100)_{YSZ} and (111)_{YSZ} epitaxial islands on (0001)_{alpha-Al_2O_3} substrates from first principles
We present an ab initio study of the interface energies of cubic
yttria-stabilized zirconia (YSZ) epitaxial layers on a (0001)_{alpha-Al_2O_3}
substrate. The interfaces are modelled using a supercell geometry and the
calculations are carried out in the framework of density-functional theory
(DFT) and the local-density approximation (LDA) using the
projector-augmented-wave (PAW) pseudopotential approach. Our calculations
clearly demonstrate that the (111)_{YSZ} || (0001)_{alpha-Al_2O_3} interface
energy is lower than that of (100)_{YSZ} || (0001)_{alpha-Al_2O_3}. This result
is central to understanding the behaviour of YSZ thin solid film islanding on
(0001)_{alpha-Al_2O_3} substrates, either flat or in presence of defects.Comment: 25 pages, 5 figures, 10 tables, submitted to Physical Review
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