157 research outputs found
Calculation of the effect of random superfluid density on the temperature dependence of the penetration depth
Microscopic variations in composition or structure can lead to nanoscale
inhomogeneity in superconducting properties such as the magnetic penetration
depth, but measurements of these properties are usually made on longer length
scales. We solve a generalized London equation with a non-uniform penetration
depth, lambda(r), obtaining an approximate solution for the disorder-averaged
Meissner effect. We find that the effective penetration depth is different from
the average penetration depth and is sensitive to the details of the disorder.
These results indicate the need for caution when interpreting measurements of
the penetration depth and its temperature dependence in systems which may be
inhomogeneous
Limits on Superconductivity-Related Magnetization in SrRuO and PrOsSb from Scanning SQUID Microscopy
We present scanning SQUID microscopy data on the superconductors Sr2RuO4 (Tc
= 1.5 K) and PrOsSb (Tc = 1.8 K). In both of these materials,
superconductivity-related time-reversal symmetry-breaking fields have been
observed by muon spin rotation; our aim was to visualize the structure of these
fields. However in neither SrRuO nor PrOsSb do we observe
spontaneous superconductivity-related magnetization. In SrRuO, many
experimental results have been interpreted on the basis of a
superconducting order parameter. This order parameter is expected to give
spontaneous magnetic induction at sample edges and order parameter domain
walls. Supposing large domains, our data restrict domain wall and edge fields
to no more than ~0.1% and ~0.2% of the expected magnitude, respectively.
Alternatively, if the magnetization is of the expected order, the typical
domain size is limited to ~30 nm for random domains, or ~500 nm for periodic
domains.Comment: 8 pages, 7 figures. Submitted to Phys. Rev.
Evidence for Nodal Superconductivity in LaFePO from Scanning SQUID Susceptometry
We measure changes in the penetration depth of the
K superconductor LaFePO. In the process scanning SQUID susceptometry is
demonstrated as a technique for accurately measuring {\it local}
temperature-dependent changes in , making it ideal for studying early
or difficult-to-grow materials. of LaFePO is found to vary linearly
with temperature from 0.36 to 2 K, with a slope of 14315 \AA/K,
suggesting line nodes in the superconducting order parameter. The linear
dependence up to is similar to the cuprate superconductors,
indicating well-developed nodes.Comment: 4 pages, 5 figure
Local measurement of the superfluid density in the pnictide superconductor Ba(FeCo)As across the superconducting dome
We measure the penetration depth in
Ba(FeCo)As using local techniques that do not average
over the sample. The superfluid density
has three main features. First, falls sharply on the underdoped
side of the dome. Second, is flat at low at optimal
doping, indicating fully gapped superconductivity, but varies more strongly in
underdoped and overdoped samples, consistent with either a power law or a small
second gap. Third, varies steeply near for optimal and
underdoping. These observations are consistent with an interplay between
magnetic and superconducting phases
Local measurement of the penetration depth in the pnictide superconductor Ba(FeCo)As
We use magnetic force microscopy (MFM) and scanning SQUID susceptometry to
measure the local superfluid density in
Ba(FeCo)As single crystals from 0.4 K to the critical
temperature K. We observe that the penetration depth
varies about ten times more slowly with temperature than previously published,
with a dependence that can be well described by a clean two-band fully gapped
model. We demonstrate that MFM can measure the important and hard-to-determine
absolute value of , as well as obtain its temperature dependence and
spatial homogeneity. We find to be uniform despite the highly
disordered vortex pinning
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Scanning SQUID microscopy on polycrystalline SmFeAsO_{0.85} and NdFeAsO_{0.94}F_{0.06}
The order parameter of the recently-discovered ferric arsenide family of superconductors remains uncertain. Some early experiments on polycrystalline samples suggested line nodes in the order parameter, however later experiments on single crystals have strongly supported fully-gapped superconductivity. An absence of nodes does not rule out unconventional order: {pi} phase shifts between the separate Fermi sheets and time-reversal symmetry-breaking components in the order parameter remain possibilities. One test for unconventional order is scanning magnetic microscopy on well-coupled polycrystalline samples: d- or p-wave order would result in orbital frustration, leading to spontaneous currents and magnetization in the superconducting state. We have performed scanning SQUID microscopy on SmFeAsO{sub 0.85} and NdFeAsO{sub 0.94}F{sub 0.06}, and in neither material do we find spontaneous orbital currents, ruling out p- or d-wave order
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Limits on the Superconducting Order Parameter in NdFeAsO_{1-x}F_y from Scanning SQUID Microscopy
Identifying the symmetry of the superconducting order parameter in the recently-discovered ferrooxypnictide family of superconductors, RFeAsO{sub 1-x}F{sub y}, where R is a rare earth, is a high priority. Many of the proposed order parameters have internal {pi} phase shifts, like the d-wave order found in the cuprates, which would result in direction-dependent phase shifts in tunneling. In dense polycrystalline samples, these phase shifts in turn would result in spontaneous orbital currents and magnetization in the superconducting state. We perform scanning SQUID microscopy on a dense polycrystalline sample of NdFeAsO{sub 0.94}F{sub 0.06} with T{sub c} = 48K and find no such spontaneous currents, ruling out many of the proposed order parameters
Transcriptional responses to glucose in Saccharomyces cerevisiae strains lacking a functional protein kinase A
Background The pattern of gene transcripts in the yeast Saccharomyces cerevisiae is strongly affected by the presence of glucose. An increased activity of protein kinase A (PKA), triggered by a rise in the intracellular concentration of cAMP, can account for many of the effects of glucose on transcription. In S. cerevisiae three genes, TPK1, TPK2, and TPK3, encode catalytic subunits of PKA. The lack of viability of tpk1 tpk2 tpk3 triple mutants may be suppressed by mutations such as yak1 or msn2/msn4. To investigate the requirement for PKA in glucose control of gene expression, we have compared the effects of glucose on global transcription in a wild-type strain and in two strains devoid of PKA activity, tpk1 tpk2 tpk3 yak1 and tpk1 tpk2 tpk3 msn2 msn4. Results We have identified different classes of genes that can be induced -or repressed- by glucose in the absence of PKA. Representative examples are genes required for glucose utilization and genes involved in the metabolism of other carbon sources, respectively. Among the genes responding to glucose in strains devoid of PKA some are also controlled by a redundant signalling pathway involving PKA activation, while others are not affected when PKA is activated through an increase in cAMP concentration. On the other hand, among genes that do not respond to glucose in the absence of PKA, some give a full response to increased cAMP levels, even in the absence of glucose, while others appear to require the cooperation of different signalling pathways. We show also that, for a number of genes controlled by glucose through a PKA-dependent pathway, the changes in mRNA levels are transient. We found that, in cells grown in gluconeogenic conditions, expression of a small number of genes, mainly connected with the response to stress, is reduced in the strains lacking PKA. Conclusions In S. cerevisiae, the transcriptional responses to glucose are triggered by a variety of pathways, alone or in combination, in which PKA is often involved. Redundant signalling pathways confer a greater robustness to the response to glucose, while cooperative pathways provide a greater flexibility.BT/BiotechnologyApplied Science
In Support of a Patient-Driven Initiative and Petition to Lower the High Price of Cancer Drugs
Comment in
Lowering the High Cost of Cancer Drugs--III. [Mayo Clin Proc. 2016]
Lowering the High Cost of Cancer Drugs--I. [Mayo Clin Proc. 2016]
Lowering the High Cost of Cancer Drugs--IV. [Mayo Clin Proc. 2016]
In Reply--Lowering the High Cost of Cancer Drugs. [Mayo Clin Proc. 2016]
US oncologists call for government regulation to curb drug price rises. [BMJ. 2015
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