86 research outputs found
Unconventional aspects of electronic transport in delafossite oxides
The electronic transport properties of the delafossite oxides ABO are
usually understood in terms of two well separated entities, namely, the
triangular A and (BO) layers. Here we review several cases among
this extensive family of materials where the transport depends on the
interlayer coupling and displays unconventional properties. We review the doped
thermoelectrics based on CuRhO and CuCrO, which show a high-temperature
recovery of Fermi-liquid transport exponents, as well as the highly anisotropic
metals PdCoO, PtCoO and PdCrO where the sheer simplicity of the
Fermi surface leads to unconventional transport. We present some of the
theoretical tools that have been used to investigate these transport properties
and review what can and cannot be learned from the extensive set of electronic
structure calculations that have been performed.Comment: 35 pages, 19 figure
Large anisotropic thermal conductivity of intrinsically two-dimensional metallic oxide PdCoO
The highly conductive layered metallic oxide \pdcoo{} is a near-perfect
analogue to an alkali metal in two dimensions. It is distinguished from other
two-dimensional electron systems where the Fermi surface does not reach the
Brillouin zone boundary by a high planar electron density exceeding
cm. The simple single-band quasi-2D electronic structure results in
strongly anisotropic transport properties and limits the effectiveness of
electron-phonon scattering. Measurements on single crystals in the temperature
range from 10-300K show that the thermal conductivity is much more weakly
anisotropic than the electrical resistivity, as a result of significant phonon
heat transport. The in-plane thermoelectric power is linear in temperature at
300\,K and displays a purity-dependent peak around 50K. Given the extreme
simplicity of the band-structure, it is possible to identify this peak with
phonon drag driven by normal electron-phonon scattering processes.Comment: 3 figure
Mg substitution in CuCrO2 delafossite compounds
A detailed investigation of the series CuCr(1-x)MgxO2 (x = 0.0 - 0.05) has
been performed by making high-temperature resistivity and thermopower
measurements, and by performing a theoretical analysis of the latter.
Microstructure characterization has been carried out as well. Upon Mg2+ for
Cr3+ substitution, a concomitant decrease in the electrical resistivity and
thermopower values is found, up to x ~ 0.02 - 0.03, indicating a low solubility
limit of Mg in the structure. This result is corroborated by scanning electron
microscopy observations, showing the presence of MgCr2O4 spinels as soon as x =
0.005. The thermopower is discussed in the temperature-independent correlation
functions ratio approximation as based on the Kubo formalism, and the
dependence of the effective charge carrier density on the nominal Mg
substitution rate is addressed. This leads to a solubility limit of 1.1% Mg in
the delafossite, confirmed by energy dispersive X-ray spectroscopy analysis.Comment: 6 pages, 5 figure
Dual electronic states in thermoelectric cobalt oxide
We investigate the low temperature magnetic field dependence of the
resistivity in the thermoelectric misfit cobalt oxide [Bi1.7Ca2O4]0.59CoO2 from
60 K down to 3 K. The scaling of the negative magnetoresistance demonstrates a
spin dependent transport mechanism due to a strong Hund's coupling. The
inferred microscopic description implies dual electronic states which explain
the coexistence between localized and itinerant electrons both contributing to
the thermopower. By shedding a new light on the electronic states which lead to
a high thermopower, this result likely provides a new potential way to optimize
the thermoelectric properties
Resistance to Mucosal Lysozyme Compensates for the Fitness Deficit of Peptidoglycan Modifications by Streptococcus pneumoniae
The abundance of lysozyme on mucosal surfaces suggests that successful colonizers must be able to evade its antimicrobial effects. Lysozyme has a muramidase activity that hydrolyzes bacterial peptidoglycan and a non-muramidase activity attributable to its function as a cationic antimicrobial peptide. Two enzymes (PgdA, a N-acetylglucosamine deacetylase, and Adr, an O-acetyl transferase) that modify different sites on the peptidoglycan of Streptococcus pneumoniae have been implicated in its resistance to lysozyme in vitro. Here we show that the antimicrobial effect of human lysozyme is due to its muramidase activity and that both peptidoglycan modifications are required for full resistance by pneumococci. To examine the contribution of lysozyme and peptidoglycan modifications during colonization of the upper respiratory tract, competition experiments were performed with wild-type and pgdAadr mutant pneumococci in lysozyme M-sufficient (LysM+/+) and -deficient (LysM−/−) mice. The wild-type strain out-competed the double mutant in LysM+/+, but not LysM−/− mice, indicating the importance of resistance to the muramidase activity of lysozyme during mucosal colonization. In contrast, strains containing single mutations in either pgdA or adr prevailed over the wild-type strain in both LysM+/+ and LysM−/− mice. Our findings demonstrate that individual peptidoglycan modifications diminish fitness during colonization. The competitive advantage of wild-type pneumococci in LysM+/+ but not LysM−/− mice suggests that the combination of peptidoglycan modifications reduces overall fitness, but that this is outweighed by the benefits of resistance to the peptidoglycan degrading activity of lysozyme
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