51 research outputs found
Electron localization and possible phase separation in the absence of a charge density wave in single-phase 1T-VS
We report on a systematic study of the structural, magnetic and transport
properties of high-purity 1T-VS powder samples prepared under high
pressure. The results differ notably from those previously obtained by
de-intercalating Li from LiVS. First, no Charge Density Wave (CDW) is found
by transmission electron microscopy down to 94 K. Though, \textit{ab initio}
phonon calculations unveil a latent CDW instability driven by an acoustic
phonon softening at the wave vector (0.21,0.21,0)
previously reported in de-intercalated samples. A further indication of latent
lattice instability is given by an anomalous expansion of the V-S bond distance
at low temperature. Second, infrared optical absorption and electrical
resistivity measurements give evidence of non metallic properties, consistent
with the observation of no CDW phase. On the other hand, magnetic
susceptibility and NMR data suggest the coexistence of localized moments with
metallic carriers, in agreement with \textit{ab initio} band structure
calculations. This discrepancy is reconciled by a picture of electron
localization induced by disorder or electronic correlations leading to a phase
separation of metallic and non-metallic domains in the nm scale. We conclude
that 1T-VS is at the verge of a CDW transition and suggest that residual
electronic doping in Li de-intercalated samples stabilizes a uniform CDW phase
with metallic properties.Comment: 22 pages, 10 Figures. Full resolution pictures available at
http://journals.aps.org/prb/abstract/10.1103/PhysRevB.89.23512
Associations Between Anesthetic Variables and Functional Outcome in Dogs With Thoracolumbar Intervertebral Disk Extrusion Undergoing Decompressive Hemilaminectomy
A tale of two stories: astrocyte regulation of synaptic depression and facilitation
Short-term presynaptic plasticity designates variations of the amplitude of
synaptic information transfer whereby the amount of neurotransmitter released
upon presynaptic stimulation changes over seconds as a function of the neuronal
firing activity. While a consensus has emerged that changes of the synapse
strength are crucial to neuronal computations, their modes of expression in
vivo remain unclear. Recent experimental studies have reported that glial
cells, particularly astrocytes in the hippocampus, are able to modulate
short-term plasticity but the underlying mechanism is poorly understood. Here,
we investigate the characteristics of short-term plasticity modulation by
astrocytes using a biophysically realistic computational model. Mean-field
analysis of the model unravels that astrocytes may mediate counterintuitive
effects. Depending on the expressed presynaptic signaling pathways, astrocytes
may globally inhibit or potentiate the synapse: the amount of released
neurotransmitter in the presence of the astrocyte is transiently smaller or
larger than in its absence. But this global effect usually coexists with the
opposite local effect on paired pulses: with release-decreasing astrocytes most
paired pulses become facilitated, while paired-pulse depression becomes
prominent under release-increasing astrocytes. Moreover, we show that the
frequency of astrocytic intracellular Ca2+ oscillations controls the effects of
the astrocyte on short-term synaptic plasticity. Our model explains several
experimental observations yet unsolved, and uncovers astrocytic
gliotransmission as a possible transient switch between short-term paired-pulse
depression and facilitation. This possibility has deep implications on the
processing of neuronal spikes and resulting information transfer at synapses.Comment: 93 pages, manuscript+supplementary text, 10 main figures, 11
supplementary figures, 1 tabl
CMS physics technical design report : Addendum on high density QCD with heavy ions
Peer reviewe
Roles of glial cells in synapse development
Brain function relies on communication among neurons via highly specialized contacts, the synapses, and synaptic dysfunction lies at the heart of age-, disease-, and injury-induced defects of the nervous system. For these reasons, the formation—and repair—of synaptic connections is a major focus of neuroscience research. In this review, I summarize recent evidence that synapse development is not a cell-autonomous process and that its distinct phases depend on assistance from the so-called glial cells. The results supporting this view concern synapses in the central nervous system as well as neuromuscular junctions and originate from experimental models ranging from cell cultures to living flies, worms, and mice. Peeking at the future, I will highlight recent technical advances that are likely to revolutionize our views on synapse–glia interactions in the developing, adult and diseased brain
Low-Potential Sodium Insertion in a NASICON-Type Structure through the Ti(III)/Ti(II) Redox Couple
We report the direct
synthesis of powder Na<sub>3</sub>Ti<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> together with its low-potential electrochemical
performance and crystal structure elucidation for the reduced and
oxidized phases. First-principles calculations at the density functional
theory level have been performed to gain further insight into the
electrochemistry of Ti(IV)/Ti(III) and Ti(III)/Ti(II) redox couples
in these sodium superionic conductor (NASICON) compounds. Finally,
we have validated the concept of full-titanium-based sodium ion cells
through the assembly of symmetric cells involving Na<sub>3</sub>Ti<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> as both positive and negative
electrode materials operating at an average potential of 1.7 V
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