Velocity renormalization and carrier lifetime in graphene from the electron-phonon interaction

We present a first-principles investigation of the phonon-induced electron self-energy in graphene. The energy dependence of the self-energy reflects the peculiar linear band structure of graphene and deviates substantially from the usual metallic behavior. The effective band velocity of the Dirac fermions is found to be reduced by 4%-8%, depending on doping, by the interaction with lattice vibrations. Our results are consistent with the observed linear dependence of the electronic linewidth on the binding energy in photoemission spectra.     

Nitrogen atom energy distributions in a hollow-cathode planar sputtering magnetron

Energy distributions of nitrogen atoms (N) in a hollow-cathode planar sputtering magnetron were obtained by use of optical emission spectroscopy. A characteristic line, N I 8216.3 A, well separated from molecular nitrogen emission bands, was identified. Jansson's nonlinear spectral deconvolution method, refined by minimization of chi(2)(w), was used to obtain the optimal deconvolved spectra. These showed nitrogen atom energies from 1 eV to beyond 500 eV. Based on comparisons with VFTRIM computer code results, it is proposed that the energetic N's are generated from N+2 ions after these ions are accelerated through the sheath and dissociatively reflect from the cathode.     

Influence of place synchrony on detection of a sinusoid

A series of experiments was performed to study the ability of the ear to code the temporal envelope of a waveform as demonstrated by comodulation masking release (CMR). The stimulus for all experiments was composed of a tone-burst signal, a 100-Hz-wide masker band centered at the signal frequency, and a second 100-Hz-wide noise band of variable frequency, the cue band. The cue band had a temporal envelope which was either correlated with or independent of that of the masker. The signal was a 100-Hz tone burst for most experiments. For the monotic stimulus, the correlated cue band results in lowered signal detection thresholds over a range extending from around 2/3 oct below the signal frequency to 1/3 oct above that frequency. When measured dichotically, with the signal and masker band in one ear and the cue band in the opposite ear, that effective range is expanded but the detection threshold shifts are a bit smaller. The greatest CMR is observed when the stimulus is presented diotically. With regard to effects of level and frequency, our data show CMR increasing with increasing stimulus level for a cue band lower in frequency than the signal, but show little effect of level for a cue band higher in frequency. Similarly, CMR increases with increasing stimulus frequency when the cue band is lower in frequency, but shows little effect of frequency for a cue band higher in frequency.     

MRI contrast-dose relationship of manganese(III)tetra(4-sulfonatophenyl) porphyrin with human xenograft tumors in nude mice at 2.0 T

Previously we reported that Mn(III)tetra(4-sulfonatophenyl) porphyrin, MnTPPS₄, is a contrast agent which can effectively enhance tumor detection by MRI. By imaging 30 additional athymic nude mice bearing subcutaneous MCF-7 WT human breast carcinoma xenografts, we have extended dose-contrast relationships over a wide range of intraperitoneal (IP) doses ranging from 0.025 to 0.50 mmol/kg. The benefits of IP injection are higher possible doses on a volume basis and a reduction in toxicity versus IV administration. Full coronal cross-section images have been obtained on a 2-T spectrometer. Although individual tumor masses displayed different distribution patterns, reflective of their internal morphology, single doses of 0.10 mmol/kg or greater were necessary to produce a detectable effect. At a dose of 0.50 mmol/kg, marked enhancement was produced. Multiple small dosages administered over the course of several days before imaging did not produce increased enhancement. Preliminary results on the new porphyrin derivative, MnTPPS₃, indicate that the ratio of the toxic dose to the effective dose may be adjustable to render this class of agents clinically useful.