2,916 research outputs found
Andreev Reflection without Fermi surface alignment in High T-Topological heterostructures
We address the controversy over the proximity effect between topological
materials and high T superconductors. Junctions are produced between
BiSrCaCuO and materials with different Fermi
surfaces (BiTe \& graphite). Both cases reveal tunneling spectra
consistent with Andreev reflection. This is confirmed by magnetic field that
shifts features via the Doppler effect. This is modeled with a single parameter
that accounts for tunneling into a screening supercurrent. Thus the tunneling
involves Cooper pairs crossing the heterostructure, showing the Fermi surface
mis-match does not hinder the ability to form transparent interfaces, which is
accounted for by the extended Brillouin zone and different lattice symmetries
Evidence for a New Excitation at the Interface Between a High-Tc Superconductor and a Topological Insulator
High-temperature superconductors exhibit a wide variety of novel excitations.
If contacted with a topological insulator, the lifting of spin rotation
symmetry in the surface states can lead to the emergence of unconventional
superconductivity and novel particles. In pursuit of this possibility, we
fabricated high critical-temperature (Tc ~ 85 K) superconductor/topological
insulator (Bi2Sr2CaCu2O8+delta/Bi2Te2Se) junctions. Below 75 K, a zero-bias
conductance peak (ZBCP) emerges in the differential conductance spectra of this
junction. The magnitude of the ZBCP is suppressed at the same rate for magnetic
fields applied parallel or perpendicular to the junction. Furthermore, it can
still be observed and does not split up to at least 8.5 T. The temperature and
magnetic field dependence of the excitation we observe appears to fall outside
the known paradigms for a ZBCP
A Revised Design for Microarray Experiments to Account for Experimental Noise and Uncertainty of Probe Response
Background
Although microarrays are analysis tools in biomedical research, they are known to yield noisy output that usually requires experimental confirmation. To tackle this problem, many studies have developed rules for optimizing probe design and devised complex statistical tools to analyze the output. However, less emphasis has been placed on systematically identifying the noise component as part of the experimental procedure. One source of noise is the variance in probe binding, which can be assessed by replicating array probes. The second source is poor probe performance, which can be assessed by calibrating the array based on a dilution series of target molecules. Using model experiments for copy number variation and gene expression measurements, we investigate here a revised design for microarray experiments that addresses both of these sources of variance.
Results
Two custom arrays were used to evaluate the revised design: one based on 25 mer probes from an Affymetrix design and the other based on 60 mer probes from an Agilent design. To assess experimental variance in probe binding, all probes were replicated ten times. To assess probe performance, the probes were calibrated using a dilution series of target molecules and the signal response was fitted to an adsorption model. We found that significant variance of the signal could be controlled by averaging across probes and removing probes that are nonresponsive or poorly responsive in the calibration experiment. Taking this into account, one can obtain a more reliable signal with the added option of obtaining absolute rather than relative measurements.
Conclusion
The assessment of technical variance within the experiments, combined with the calibration of probes allows to remove poorly responding probes and yields more reliable signals for the remaining ones. Once an array is properly calibrated, absolute quantification of signals becomes straight forward, alleviating the need for normalization and reference hybridizations
Experimentally Engineering the Edge Termination of Graphene Nanoribbons
The edges of graphene nanoribbons (GNRs) have attracted much interest due to
their potentially strong influence on GNR electronic and magnetic properties.
Here we report the ability to engineer the microscopic edge termination of high
quality GNRs via hydrogen plasma etching. Using a combination of
high-resolution scanning tunneling microscopy and first-principles
calculations, we have determined the exact atomic structure of plasma-etched
GNR edges and established the chemical nature of terminating functional groups
for zigzag, armchair and chiral edge orientations. We find that the edges of
hydrogen-plasma-etched GNRs are generally flat, free of structural
reconstructions and are terminated by hydrogen atoms with no rehybridization of
the outermost carbon edge atoms. Both zigzag and chiral edges show the presence
of edge states.Comment: 16+9 pages, 3+4 figure
A Metabolomics Approach for Predicting OATP1B-Type Transporter-Mediated Drug-Drug Interaction Liabilities
In recent years, various endogenous compounds have been proposed as putative biomarkers for the hepatic uptake transporters OATP1B1 and OATP1B3 that have the potential to predict transporter-mediated drug-drug interactions (DDIs). However, these compounds have often been identified from top-down strategies and have not been fully utilized as a substitute for traditional DDI studies. In an attempt to eliminate observer bias in biomarker selection, we applied a bottom-up, untargeted metabolomics screening approach in mice and found that plasma levels of the conjugated bile acid chenodeoxycholate-24-glucuronide (CDCA-24G) are particularly sensitive to deletion of the orthologous murine transporter Oatp1b2 (31-fold increase vs. wild type) or the entire Oatp1a/1b(-/-)cluster (83-fold increased), whereas the humanized transgenic overexpression of hepatic OATP1B1 or OATP1B3 resulted in the partial restoration of transport function. Validation studies with the OATP1B1/OATP1B3 inhibitors rifampin and paclitaxel in vitro as well as in mice and human subjects confirmed that CDCA-24G is a sensitive and rapid response biomarker to dose-dependent transporter inhibition. Collectively, our study confirmed the ability of CDCA-24G to serve as a sensitive and selective endogenous biomarker of OATP1B-type transport function and suggests a template for the future development of biomarkers for other clinically important xenobiotic transporters.</p
Band gaps of primary metallic carbon nanotubes
Primary metallic, or small gap semiconducting nanotubes, are tubes with band
gaps that arise solely from breaking the bond symmetry due to the curvature. We
derive an analytic expression for these gaps by considering how a general
symmetry breaking opens a gap in nanotubes with a well defined chiral wrapping
vector. This approach provides a straightforward way to include all types of
symmetry breaking effects, resulting in a simple unified gap equation as a
function of chirality and deformations.Comment: Final published version. Four pages in revtex format including one
epsf-embedded figure. The latest version in PDF format is available from
http://fy.chalmers.se/~eggert/papers/nanodeform.pd
Gate-Controlled Ionization and Screening of Cobalt Adatoms on a Graphene Surface
We describe scanning tunneling spectroscopy (STS) measurements performed on
individual cobalt (Co) atoms deposited onto backgated graphene devices. We find
that Co adatoms on graphene can be ionized by either the application of a
global backgate voltage or by the application of a local electric field from a
scanning tunneling microscope (STM) tip. Large screening clouds are observed to
form around Co adatoms ionized in this way, and we observe that some intrinsic
graphene defects display a similar behavior. Our results provide new insight
into charged impurity scattering in graphene, as well as the possibility of
using graphene devices as chemical sensors.Comment: 19 pages, 4 figure
Direct observation of active material concentration gradients and crystallinity breakdown in LiFePO4 electrodes during charge/discharge cycling of lithium batteries
The phase changes that occur during discharge of an electrode comprised of LiFePO4, carbon, and PTFE binder have been studied in lithium half cells by using X-ray diffraction measurements in reflection geometry. Differences in the state of charge between the front and the back of LiFePO4 electrodes have been visualized. By modifying the X-ray incident angle the depth of penetration of the X-ray beam into the electrode was altered, allowing for the examination of any concentration gradients that were present within the electrode. At high rates of discharge the electrode side facing the current collector underwent limited lithium insertion while the electrode as a whole underwent greater than 50% of discharge. This behavior is consistent with depletion at high rate of the lithium content of the electrolyte contained in the electrode pores. Increases in the diffraction peak widths indicated a breakdown of crystallinity within the active material during cycling even during the relatively short duration of these experiments, which can also be linked to cycling at high rate
Effects of anharmonic strain on phase stability of epitaxial films and superlattices: applications to noble metals
Epitaxial strain energies of epitaxial films and bulk superlattices are
studied via first-principles total energy calculations using the local-density
approximation. Anharmonic effects due to large lattice mismatch, beyond the
reach of the harmonic elasticity theory, are found to be very important in
Cu/Au (lattice mismatch 12%), Cu/Ag (12%) and Ni/Au (15%). We find that
is the elastically soft direction for biaxial expansion of Cu and Ni, but it is
for large biaxial compression of Cu, Ag, and Au. The stability of
superlattices is discussed in terms of the coherency strain and interfacial
energies. We find that in phase-separating systems such as Cu-Ag the
superlattice formation energies decrease with superlattice period, and the
interfacial energy is positive. Superlattices are formed easiest on (001) and
hardest on (111) substrates. For ordering systems, such as Cu-Au and Ag-Au, the
formation energy of superlattices increases with period, and interfacial
energies are negative. These superlattices are formed easiest on (001) or (110)
and hardest on (111) substrates. For Ni-Au we find a hybrid behavior:
superlattices along and like in phase-separating systems, while for
they behave like in ordering systems. Finally, recent experimental
results on epitaxial stabilization of disordered Ni-Au and Cu-Ag alloys,
immiscible in the bulk form, are explained in terms of destabilization of the
phase separated state due to lattice mismatch between the substrate and
constituents.Comment: RevTeX galley format, 16 pages, includes 9 EPS figures, to appear in
Physical Review
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