900 research outputs found
Effects of electron-phonon interactions on the electron tunneling spectrum of PbS quantum dots
We present a tunnel spectroscopy study of single PbS Quantum Dots (QDs) as
function of temperature and gate voltage. Three distinct signatures of strong
electron-phonon coupling are observed in the Electron Tunneling Spectrum (ETS)
of these QDs. In the shell-filling regime, the degeneracy of the
electronic levels is lifted by the Coulomb interactions and allows the
observation of phonon sub-bands that result from the emission of optical
phonons. At low bias, a gap is observed in the ETS that cannot be closed with
the gate voltage, which is a distinguishing feature of the Franck-Condon (FC)
blockade. From the data, a Huang-Rhys factor in the range is
obtained. Finally, in the shell tunneling regime, the optical phonons appear in
the inelastic ETS .Comment: 5 pages, 5 figure
Autocorrelation analysis for the unbiased determination of power-law exponents in single-quantum-dot blinking
We present an unbiased and robust analysis method for power-law blinking
statistics in the photoluminescence of single nano-emitters, allowing us to
extract both the bright- and dark-state power-law exponents from the emitters'
intensity autocorrelation functions. As opposed to the widely-used threshold
method, our technique therefore does not require discriminating the emission
levels of bright and dark states in the experimental intensity timetraces. We
rely on the simultaneous recording of 450 emission timetraces of single
CdSe/CdS core/shell quantum dots at a frame rate of 250 Hz with single photon
sensitivity. Under these conditions, our approach can determine ON and OFF
power-law exponents with a precision of 3% from a comparison to numerical
simulations, even for shot-noise-dominated emission signals with an average
intensity below 1 photon per frame and per quantum dot. These capabilities pave
the way for the unbiased, threshold-free determination of blinking power-law
exponents at the micro-second timescale
Effect of short range order on electronic and magnetic properties of disordered Co based alloys
We here study electronic structure and magnetic properties of disordered CoPd
and CoPt alloys using Augmented Space Recursion technique coupled with the
tight-binding linearized muffin tin orbital (TB-LMTO) method. Effect of short
range ordering present in disordered phase of alloys on electronic and magnetic
properties has been discussed. We present results for magnetic moments, Curie
temperatures and electronic band energies with varying degrees of short range
order for different concentrations of Co and try to understand and compare the
magnetic properties and ordering phenomena in these systems.Comment: 15 pages,17 postscript figures,uses own style file
Topological correlations and asymptotic freedom in cellular aggregates
In random cellular systems, both observation and maximum entropy inference
give a specific form to the topological pair correlation: it is bi-affine in
the cells number of edges with coefficients depending on the distance between
the two cells of the pair. Assuming this form for the pair correlations, we
make explicit the conditions of statistical independence at large distance.
When, on average, the defects do not contribute, the layer population and the
enclosed topological charge both increase polynomially with distance. In
dimension 2, the exponent of the leading terms depend on sum rules satisfied,
or not, by the maximum entropy coefficients.Comment: Available online at http://www.sciencedirect.co
Addressing the exciton fine structure in colloidal nanocrystals: the case of CdSe nanoplatelets
We study the band-edge exciton fine structure and in particular its
bright-dark splitting in colloidal semiconductor nanocrystals by four different
optical methods based on fluorescence line narrowing and time-resolved
measurements at various temperatures down to 2 K. We demonstrate that all these
methods provide consistent splitting values and discuss their advances and
limitations. Colloidal CdSe nanoplatelets with thicknesses of 3, 4 and 5
monolayers are chosen for experimental demonstrations. The bright-dark
splitting of excitons varies from 3.2 to 6.0 meV and is inversely proportional
to the nanoplatelet thickness. Good agreement between experimental and
theoretically calculated size dependence of the bright-dark exciton slitting is
achieved. The recombination rates of the bright and dark excitons and the
bright to dark relaxation rate are measured by time-resolved techniques
PEG Branched Polymer for Functionalization of Nanomaterials with Ultralong Blood Circulation
Nanomaterials have been actively pursued for biological and medical
applications in recent years. Here, we report the synthesis of several new
poly(ethylene glycol) grafted branched-polymers for functionalization of
various nanomaterials including carbon nanotubes, gold nanoparticles (NP) and
gold nanorods (NRs), affording high aqueous solubility and stability for these
materials. We synthesize different surfactant polymers based upon
poly-(g-glutamic acid) (gPGA) and poly(maleic anhydride-alt-1-octadecene)
(PMHC18). We use the abundant free carboxylic acid groups of gPGA for attaching
lipophilic species such as pyrene or phospholipid, which bind to nanomaterials
via robust physisorption. Additionally, the remaining carboxylic acids on gPGA
or the amine-reactive anhydrides of PMHC18 are then PEGylated, providing
extended hydrophilic groups, affording polymeric amphiphiles. We show that
single-walled carbon nanotubes (SWNTs), Au NPs and NRs functionalized by the
polymers exhibit high stability in aqueous solutions at different pHs, at
elevated temperatures and in serum. Morever, the polymer-coated SWNTs exhibit
remarkably long blood circulation (t1/2 22.1 h) upon intravenous injection into
mice, far exceeding the previous record of 5.4 h. The ultra-long blood
circulation time suggests greatly delayed clearance of nanomaterials by the
reticuloendothelial system (RES) of mice, a highly desired property for in vivo
applications of nanomaterials, including imaging and drug delivery
Quasi-stationary regime of a branching random walk in presence of an absorbing wall
A branching random walk in presence of an absorbing wall moving at a constant
velocity undergoes a phase transition as the velocity of the wall
varies. Below the critical velocity , the population has a non-zero
survival probability and when the population survives its size grows
exponentially. We investigate the histories of the population conditioned on
having a single survivor at some final time . We study the quasi-stationary
regime for when is large. To do so, one can construct a modified
stochastic process which is equivalent to the original process conditioned on
having a single survivor at final time . We then use this construction to
show that the properties of the quasi-stationary regime are universal when
. We also solve exactly a simple version of the problem, the
exponential model, for which the study of the quasi-stationary regime can be
reduced to the analysis of a single one-dimensional map.Comment: 2 figures, minor corrections, one reference adde
Крещение Крыма
Цель статьи - определить место и значение фестивной культуры в условиях социальных трансформаций
Integrins as therapeutic targets: lessons and opportunities.
The integrins are a large family of cell adhesion molecules that are essential for the regulation of cell growth and function. The identification of key roles for integrins in a diverse range of diseases, including cancer, infection, thrombosis and autoimmune disorders, has revealed their substantial potential as therapeutic targets. However, so far, pharmacological inhibitors for only three integrins have received marketing approval. This article discusses the structure and function of integrins, their roles in disease and the chequered history of the approved integrin antagonists. Recent advances in the understanding of integrin function, ligand interaction and signalling pathways suggest novel strategies for inhibiting integrin function that could help harness their full potential as therapeutic targets
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