152 research outputs found
Orbital Selective Pressure-Driven Metal-Insulator Transition in FeO from Dynamical Mean-Field Theory
In this Letter we report the first LDA+DMFT (method combining Local Density
Approximation with Dynamical Mean-Field Theory) results of magnetic and
spectral properties calculation for paramagnetic phases of FeO at ambient and
high pressures (HP). At ambient pressure (AP) calculation gave FeO as a Mott
insulator with Fe 3-shell in high-spin state. Calculated spectral functions
are in a good agreement with experimental PES and IPES data. Experimentally
observed metal-insulator transition at high pressure is successfully reproduced
in calculations. In contrast to MnO and FeO ( configuration) where
metal-insulator transition is accompanied by high-spin to low-spin transition,
in FeO ( configuration) average value of magnetic moment
is nearly the same in the insulating phase at AP and
metallic phase at HP in agreement with X-Ray spectroscopy data (Phys. Rev.
Lett. {\bf83}, 4101 (1999)). The metal-insulator transition is orbital
selective with only orbitals demonstrating spectral function typical
for strongly correlated metal (well pronounced Hubbard bands and narrow
quasiparticle peak) while states remain insulating.Comment: 4 pages, 4 figure
Metal-ligand interplay in strongly-correlated oxides: a parametrized phase diagram for pressure induced spin transitions
We investigate the magnetic properties of archetypal transition-metal oxides
MnO, FeO, CoO and NiO under very high pressure by x-ray emission spectroscopy
at the K\beta line. We observe a strong modification of the magnetism in the
megabar range in all the samples except NiO. The results are analyzed within a
multiplet approach including charge-transfer effects. The pressure dependence
of the emission line is well accounted for by changes of the ligand field
acting on the d electrons and allows us to extract parameters like local
d-hybridization strength, O-2p bandwidth and ionic crystal field across the
magnetic transition. This approach allows a first-hand insight into the
mechanism of the pressure induced spin transition.Comment: 5 pages, 3 figure
Single ion implantation for single donor devices using Geiger mode detectors
Electronic devices that are designed to use the properties of single atoms
such as donors or defects have become a reality with recent demonstrations of
donor spectroscopy, single photon emission sources, and magnetic imaging using
defect centers in diamond. Improving single ion detector sensitivity is linked
to improving control over the straggle of the ion as well as providing more
flexibility in lay-out integration with the active region of the single donor
device construction zone by allowing ion sensing at potentially greater
distances. Using a remotely located passively gated single ion Geiger mode
avalanche diode (SIGMA) detector we have demonstrated 100% detection efficiency
at a distance of >75 um from the center of the collecting junction. This
detection efficiency is achieved with sensitivity to ~600 or fewer
electron-hole pairs produced by the implanted ion. Ion detectors with this
sensitivity and integrated with a thin dielectric, for example 5 nm gate oxide,
using low energy Sb implantation would have an end of range straggle of <2.5
nm. Significant reduction in false count probability is achieved by modifying
the ion beam set-up to allow for cryogenic operation of the SIGMA detector.
Using a detection window of 230 ns at 1 Hz, the probability of a false count
was measured as 1E-1 and 1E-4 for operation temperatures of 300K and 77K,
respectively. Low temperature operation and reduced false, dark, counts are
critical to achieving high confidence in single ion arrival. For the device
performance in this work, the confidence is calculated as a probability of >98%
for counting one and only one ion for a false count probability of 1E-4 at an
average ion number per gated window of 0.015.Comment: 10 pages, 5 figures, submitted to Nanotechnolog
Inelastic X-ray Scattering by Electronic Excitations in Solids at High Pressure
Investigating electronic structure and excitations under extreme conditions
gives access to a rich variety of phenomena. High pressure typically induces
behavior such as magnetic collapse and the insulator-metal transition in 3d
transition metals compounds, valence fluctuations or Kondo-like characteristics
in -electron systems, and coordination and bonding changes in molecular
solids and glasses. This article reviews research concerning electronic
excitations in materials under extreme conditions using inelastic x-ray
scattering (IXS). IXS is a spectroscopic probe of choice for this study because
of its chemical and orbital selectivity and the richness of information it
provides. Being an all-photon technique, IXS has a penetration depth compatible
with high pressure requirements. Electronic transitions under pressure in 3d
transition metals compounds and -electron systems, most of them strongly
correlated, are reviewed. Implications for geophysics are mentioned. Since the
incident X-ray energy can easily be tuned to absorption edges, resonant IXS,
often employed, is discussed at length. Finally studies involving local
structure changes and electronic transitions under pressure in materials
containing light elements are briefly reviewed.Comment: submitted to Rev. Mod. Phy
Experimental and theoretical evidence for pressure-induced metallization in FeO with the rock-salt type structure
Electrical conductivity of FeO was measured up to 141 GPa and 2480 K in a
laserheated diamond-anvil cell. The results show that rock-salt (B1) type
structured FeO metallizes at around 70 GPa and 1900 K without any structural
phase transition. We computed fully self-consistently the electronic structure
and the electrical conductivity of B1 FeO as a function of pressure and
temperature, and found that although insulating as expected at ambient
condition, B1 FeO metallizes at high temperatures, consistent with experiments.
The observed metallization is related to spin crossover
Premature Osteoblast Clustering by Enamel Matrix Proteins Induces Osteoblast Differentiation through Up-Regulation of Connexin 43 and N-Cadherin
In recent years, enamel matrix derivative (EMD) has garnered much interest in the dental field for its apparent bioactivity that stimulates regeneration of periodontal tissues including periodontal ligament, cementum and alveolar bone. Despite its widespread use, the underlying cellular mechanisms remain unclear and an understanding of its biological interactions could identify new strategies for tissue engineering. Previous in vitro research has demonstrated that EMD promotes premature osteoblast clustering at early time points. The aim of the present study was to evaluate the influence of cell clustering on vital osteoblast cell-cell communication and adhesion molecules, connexin 43 (cx43) and N-cadherin (N-cad) as assessed by immunofluorescence imaging, real-time PCR and Western blot analysis. In addition, differentiation markers of osteoblasts were quantified using alkaline phosphatase, osteocalcin and von Kossa staining. EMD significantly increased the expression of connexin 43 and N-cadherin at early time points ranging from 2 to 5 days. Protein expression was localized to cell membranes when compared to control groups. Alkaline phosphatase activity was also significantly increased on EMD-coated samples at 3, 5 and 7 days post seeding. Interestingly, higher activity was localized to cell cluster regions. There was a 3 fold increase in osteocalcin and bone sialoprotein mRNA levels for osteoblasts cultured on EMD-coated culture dishes. Moreover, EMD significantly increased extracellular mineral deposition in cell clusters as assessed through von Kossa staining at 5, 7, 10 and 14 days post seeding. We conclude that EMD up-regulates the expression of vital osteoblast cell-cell communication and adhesion molecules, which enhances the differentiation and mineralization activity of osteoblasts. These findings provide further support for the clinical evidence that EMD increases the speed and quality of new bone formation in vivo
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