316 research outputs found
Carrier and polarization dynamics in monolayer MoS2
In monolayer MoS2 optical transitions across the direct bandgap are governed
by chiral selection rules, allowing optical valley initialization. In time
resolved photoluminescence (PL) experiments we find that both the polarization
and emission dynamics do not change from 4K to 300K within our time resolution.
We measure a high polarization and show that under pulsed excitation the
emission polarization significantly decreases with increasing laser power. We
find a fast exciton emission decay time on the order of 4ps. The absence of a
clear PL polarization decay within our time resolution suggests that the
initially injected polarization dominates the steady state PL polarization. The
observed decrease of the initial polarization with increasing pump photon
energy hints at a possible ultrafast intervalley relaxation beyond the
experimental ps time resolution. By compensating the temperature induced change
in bandgap energy with the excitation laser energy an emission polarization of
40% is recovered at 300K, close to the maximum emission polarization for this
sample at 4K.Comment: 7 pages, 7 figures including supplementary materia
Robust optical emission polarization in MoS2 monolayers through selective valley excitation
We report polarization resolved photoluminescence from monolayer MoS2, a
two-dimensional, non-centrosymmetric crystal with direct energy gaps at two
different valleys in momentum space. The inherent chiral optical selectivity
allows exciting one of these valleys and close to 90% polarized emission at 4K
is observed with 40% polarization remaining at 300K. The high polarization
degree of the emission remains unchanged in transverse magnetic fields up to 9T
indicating robust, selective valley excitation.Comment: 5 pages, 3 figure
Gamma oscillations in V1 are correlated with GABA(A) receptor density: A multi-modal MEG and Flumazenil-PET study.
High-frequency oscillations in the gamma-band reflect rhythmic synchronization of spike timing in active neural networks. The modulation of gamma oscillations is a widely established mechanism in a variety of neurobiological processes, yet its neurochemical basis is not fully understood. Modeling, in-vitro and in-vivo animal studies suggest that gamma oscillation properties depend on GABAergic inhibition. In humans, search for evidence linking total GABA concentration to gamma oscillations has led to promising -but also to partly diverging- observations. Here, we provide the first evidence of a direct relationship between the density of GABA(A) receptors and gamma oscillatory gamma responses in human primary visual cortex (V1). By combining Flumazenil-PET (to measure resting-levels of GABA(A) receptor density) and MEG (to measure visually-induced gamma oscillations), we found that GABA(A) receptor densities correlated positively with the frequency and negatively with amplitude of visually-induced gamma oscillations in V1. Our findings demonstrate that gamma-band response profiles of primary visual cortex across healthy individuals are shaped by GABA(A)-receptor-mediated inhibitory neurotransmission. These results bridge the gap with in-vitro and animal studies and may have future clinical implications given that altered GABAergic function, including dysregulation of GABA(A) receptors, has been related to psychiatric disorders including schizophrenia and depression
11 nm hard X-ray focus from a large-aperture multilayer Laue lens
The focusing performance of a multilayer Laue lens (MLL) with 43.4 ÎŒm aperture, 4 nm finest zone width and 4.2 mm focal length at 12 keV was characterized with X-rays using ptychography method. The reconstructed probe shows a full-width-at-half-maximum (FWHM) peak size of 11.2 nm. The obtained X-ray wavefront shows excellent agreement with the dynamical calculations, exhibiting aberrations less than 0.3 wave period, which ensures the MLL capable of producing a diffraction-limited focus while offering a sufficient working distance. This achievement opens up opportunities of incorporating a variety of in-situ experiments into ultra high-resolution X-ray microscopy studies
Kak's three-stage protocol of secure quantum communication revisited: Hitherto unknown strengths and weaknesses of the protocol
Kak's three-stage protocol for quantum key distribution is revisited with
special focus on its hitherto unknown strengths and weaknesses. It is shown
that this protocol can be used for secure direct quantum communication.
Further, the implementability of this protocol in the realistic situation is
analyzed by considering various Markovian noise models. It is found that the
Kak's protocol and its variants in their original form can be implemented only
in a restricted class of noisy channels, where the protocols can be transformed
to corresponding protocols based on logical qubits in decoherence free
subspace. Specifically, it is observed that Kak's protocol can be implemented
in the presence of collective rotation and collective dephasing noise, but
cannot be implemented in its original form in the presence of other types of
noise, like amplitude damping and phase damping noise. Further, the performance
of the protocol in the noisy environment is quantified by computing average
fidelity under various noise models, and subsequently a set of preferred states
for secure communication in noisy environment have also been identified.Comment: Kak's protocol is not suitable for quantum cryptography in presence
of nois
14. Ăvaluation de la mastectomie avec reconstruction mammaire immĂ©diate par lambeau de grand dorsal, aprĂšs chimiothĂ©rapie et radiothĂ©rapie nĂ©oadjuvante
Multimodality hard-x-ray imaging of a chromosome with nanoscale spatial resolution
We developed a scanning hard x-ray microscope using a new class of x-ray nano-focusing optic called a multilayer Laue lens and imaged a chromosome with nanoscale spatial resolution. The combination of the hard x-ray's superior penetration power, high sensitivity to elemental composition, high spatial-resolution and quantitative analysis creates a unique tool with capabilities that other microscopy techniques cannot provide. Using this microscope, we simultaneously obtained absorption-, phase-, and fluorescence-contrast images of Pt-stained human chromosome samples. The high spatial-resolution of the microscope and its multi-modality imaging capabilities enabled us to observe the internal ultra-structures of a thick chromosome without sectioning it
Bacterial Genome Partitioning: N-Terminal Domain of IncC Protein Encoded by Broad-Host-Range Plasmid RK2 Modulates Oligomerisation and DNA Binding
ParAWalker ATPases form part of the machinery that promotes better-thanrandom segregation of bacterial genomes. ParA proteins normally occur in one of two forms, differing by their N-terminal domain (NTD) of approximately 100 aa, which is generally associated with site-specific DNA binding. Unusually, and for as yet unknown reasons, parA (incC) of IncP-1 plasmids is translated from alternative start codons producing two
forms, IncC1 (364 aa) and IncC2 (259 aa), whose ratio varies between hosts.IncC2 could be detected as an oligomeric form containing dimers, tetramers
and octamers, but the N-terminal extension present in IncC1 favours nucleotide-stimulated dimerisation as well as high-affinity and ATPdependent non-specific DNA binding. The IncC1 NTD does not dimerise or bind DNA alone, but it does bind IncC2 in the presence of nucleotides. Mixing IncC1 and IncC2 improved polymerisation and DNA binding. Thus,the NTD may modulate the polymerisation interface, facilitating polymerisation/
depolymerisation and DNA binding, to promote the cycle that
drives partitioning
Inverse Modeling for MEG/EEG data
We provide an overview of the state-of-the-art for mathematical methods that
are used to reconstruct brain activity from neurophysiological data. After a
brief introduction on the mathematics of the forward problem, we discuss
standard and recently proposed regularization methods, as well as Monte Carlo
techniques for Bayesian inference. We classify the inverse methods based on the
underlying source model, and discuss advantages and disadvantages. Finally we
describe an application to the pre-surgical evaluation of epileptic patients.Comment: 15 pages, 1 figur
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