810 research outputs found
Integrated Optics: a Report on the 2nd OSA Topical Meeting
This report surveys the papers presented at the 2nd OSA Topical Meeting on Integrated Optics, which was held 21–24 January 1974 in New Orleans, La
Electron-electron interaction effects on optical excitations in semiconducting single-walled carbon nanotubes
We report correlated-electron calculations of optically excited states in ten
semiconducting single-walled carbon nanotubes with a wide range of diameters.
Optical excitation occurs to excitons whose binding energies decrease with the
increasing nanotube diameter, and are smaller than the binding energy of an
isolated strand of poly-(paraphenylene vinylene). The ratio of the energy of
the second optical exciton polarized along the nanotube axis to that of the
lowest exciton is smaller than the value predicted within single-particle
theory. The experimentally observed weak photoluminescence is an intrinsic
feature of semiconducting nanotubes, and is consequence of dipole-forbidden
excitons occurring below the optical exciton.Comment: 5 pages, 3 figures, To appear in PR
Evidence for Excimer Photoexcitations in an Ordered {\pi}-Conjugated Polymer Film
We report pressure-dependent transient picosecond and continuous-wave
photomodulation studies of disordered and ordered films of
2-methoxy-5-(2-ethylhexyloxy) poly(para-phenylenevinylene). Photoinduced
absorption (PA) bands in the disordered film exhibit very weak pressure
dependence and are assigned to intrachain excitons and polarons. In contrast,
the ordered film exhibits two additional transient PA bands in the midinfrared
that blueshift dramatically with pressure. Based on high-order configuration
interaction calculations we ascribe the PA bands in the ordered film to
excimers. Our work brings insight to the exciton binding energy in ordered
films versus disordered films and solutions. The reduced exciton binding energy
in ordered films is due to new energy states appearing below the continuum band
threshold of the single strand.Comment: 5.5 pages, 5 figure
Phantom evaluation of a cardiac SPECT/VCT system that uses a common set of solid-state detectors for both emission and transmission scans
We developed a cardiac SPECT system (X-ACT) with low dose volume CT transmission-based attenuation correction (AC). Three solid-state detectors are configured to form a triple-head system for emission scans and reconfigured to form a 69-cm field-of-view detector arc for transmission scans. A near mono-energetic transmission line source is produced from the collimated fluorescence x-ray emitted from a lead target when the target is illuminated by a narrow polychromatic x-ray beam from an x-ray tube. Transmission scans can be completed in 1 min with insignificant patient dose (deep dose equivalent <5 μSv).
We used phantom studies to evaluate (1) the accuracy of the reconstructed attenuation maps, (2) the effect of AC on image uniformity, and (3) the effect of AC on defect contrast (DC). The phantoms we used included an ACR phantom, an anthropomorphic phantom with a uniform cardiac insert, and an anthropomorphic phantom with two defects in the cardiac insert.
The reconstructed attenuation coefficient of water at 140 keV was .150 ± .003/cm in the uniform region of the ACR phantom, .151 ± .003/cm and .151 ± .002/cm in the liver and cardiac regions of the anthropomorphic phantom. The ACR phantom images with AC showed correction of the bowing effect due to attenuation in the images without AC (NC). The 17-segment scores of the images of the uniform cardiac insert were 78.3 ± 6.5 before and 87.9 ± 3.3 after AC (average ± standard deviation). The inferior-to-anterior wall ratio and the septal-to-lateral wall ratio were .99 and 1.16 before and 1.02 and 1.00 after AC. The DC of the two defects was .528 and .156 before and .628 and .173 after AC.
The X-ACT system generated accurate attenuation maps with 1-minute transmission scans. AC improved image quality and uniformity over NC
The prevalence of depressive symptoms among older patients with hypertension in rural China
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/139900/1/gps4628.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/139900/2/gps4628_am.pd
Mott-Peierls Transition in the extended Peierls-Hubbard model
The one-dimensional extended Peierls-Hubbard model is studied at several band
fillings using the density matrix renormalization group method. Results show
that the ground state evolves from a Mott-Peierls insulator with a correlation
gap at half-filling to a soliton lattice with a small band gap away from
half-filling. It is also confirmed that the ground state of the Peierls-Hubbard
model undergoes a transition to a metallic state at finite doping. These
results show that electronic correlations effects should be taken into account
in theoretical studies of doped polyacetylene. They also show that a
Mott-Peierls theory could explain the insulator-metal transition observed in
this material.Comment: 4 pages with 3 embedded eps figure
Localization Properties of Electronic States in Polaron Model of poly(dG)-poly(dC) and poly(dA)-poly(dT) DNA polymers
We numerically investigate localization properties of electronic states in a
static model of poly(dG)-poly(dC) and poly(dA)-poly(dT) DNA polymers with
realistic parameters obtained by quantum-chemical calculation. The randomness
in the on-site energies caused by the electron-phonon coupling are completely
correlated to the off-diagonal parts. In the single electron model, the effect
of the hydrogen-bond stretchings, the twist angles between the base pairs and
the finite system size effects on the energy dependence of the localization
length and on the Lyapunov exponent are given. The localization length is
reduced by the influence of the fluctuations in the hydrogen bond stretchings.
It is also shown that the helical twist angle affects the localization length
in the poly(dG)-poly(dC) DNA polymer more strongly than in the
poly(dA)-poly(dT) one. Furthermore, we show resonance structures in the energy
dependence of the localization length when the system size is relatively small.Comment: 6 pages, 6 figure
Polarons with a twist
We consider a polaron model where molecular \emph{rotations} are important.
Here, the usual hopping between neighboring sites is affected directly by the
electron-phonon interaction via a {\em twist-dependent} hopping amplitude. This
model may be of relevance for electronic transport in complex molecules and
polymers with torsional degrees of freedom, such as DNA, as well as in
molecular electronics experiments where molecular twist motion is significant.
We use a tight-binding representation and find that very different polaronic
properties are already exhibited by a two-site model -- these are due to the
nonlinearity of the restoring force of the twist excitations, and of the
electron-phonon interaction in the model. In the adiabatic regime, where
electrons move in a {\em low}-frequency field of twisting-phonons, the
effective splitting of the energy levels increases with coupling strength. The
bandwidth in a long chain shows a power-law suppression with coupling, unlike
the typical exponential dependence due to linear phonons.Comment: revtex4 source and one eps figur
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