68 research outputs found
Visualizing the emergence of the pseudogap state and the evolution to superconductivity in a lightly hole-doped Mott insulator
Superconductivity emerges from the cuprate antiferromagnetic Mott state with
hole doping. The resulting electronic structure is not understood, although
changes in the state of oxygen atoms appear paramount. Hole doping first
destroys the Mott state yielding a weak insulator where electrons localize only
at low temperatures without a full energy gap. At higher doping, the
'pseudogap', a weakly conducting state with an anisotropic energy gap and
intra-unit-cell breaking of 90\degree-rotational (C4v) symmetry appears.
However, a direct visualization of the emergence of these phenomena with
increasing hole density has never been achieved. Here we report atomic-scale
imaging of electronic structure evolution from the weak-insulator through the
emergence of the pseudogap to the superconducting state in Ca2-xNaxCuO2Cl2. The
spectral signature of the pseudogap emerges at lowest doping from a weakly
insulating but C4v-symmetric matrix exhibiting a distinct spectral shape. At
slightly higher hole-density, nanoscale regions exhibiting pseudogap spectra
and 180\degree-rotational (C2v) symmetry form unidirectional clusters within
the C4v-symmetric matrix. Thus, hole-doping proceeds by the appearance of
nanoscale clusters of localized holes within which the broken-symmetry
pseudogap state is stabilized. A fundamentally two-component electronic
structure11 then exists in Ca2-xNaxCuO2Cl2 until the C2v-symmetric clusters
touch at higher doping, and the long-range superconductivity appears.Comment: See the Nature Physics website for the published version available at
http://dx.doi.org/10.1038/Nphys232
A momentum-dependent perspective on quasiparticle interference in Bi_{2}Sr_{2}CaCu_{2}O_{8+\delta}
Angle Resolved Photoemission Spectroscopy (ARPES) probes the momentum-space
electronic structure of materials, and provides invaluable information about
the high-temperature superconducting cuprates. Likewise, the cuprate
real-space, inhomogeneous electronic structure is elucidated by Scanning
Tunneling Spectroscopy (STS). Recently, STS has exploited quasiparticle
interference (QPI) - wave-like electrons scattering off impurities to produce
periodic interference patterns - to infer properties of the QP in
momentum-space. Surprisingly, some interference peaks in
Bi_{2}Sr_{2}CaCu_{2}O_{8+\delta} (Bi-2212) are absent beyond the
antiferromagnetic (AF) zone boundary, implying the dominance of particular
scattering process. Here, we show that ARPES sees no evidence of quasiparticle
(QP) extinction: QP-like peaks are measured everywhere on the Fermi surface,
evolving smoothly across the AF zone boundary. This apparent contradiction
stems from different natures of single-particle (ARPES) and two-particle (STS)
processes underlying these probes. Using a simple model, we demonstrate
extinction of QPI without implying the loss of QP beyond the AF zone boundary
Electron-Spin Excitation Coupling in an Electron Doped Copper Oxide Superconductor
High-temperature (high-Tc) superconductivity in the copper oxides arises from
electron or hole doping of their antiferromagnetic (AF) insulating parent
compounds. The evolution of the AF phase with doping and its spatial
coexistence with superconductivity are governed by the nature of charge and
spin correlations and provide clues to the mechanism of high-Tc
superconductivity. Here we use a combined neutron scattering and scanning
tunneling spectroscopy (STS) to study the Tc evolution of electron-doped
superconducting Pr0.88LaCe0.12CuO4-delta obtained through the oxygen annealing
process. We find that spin excitations detected by neutron scattering have two
distinct modes that evolve with Tc in a remarkably similar fashion to the
electron tunneling modes in STS. These results demonstrate that
antiferromagnetism and superconductivity compete locally and coexist spatially
on nanometer length scales, and the dominant electron-boson coupling at low
energies originates from the electron-spin excitations.Comment: 30 pages, 12 figures, supplementary information include
Universality of pseudogap and emergent order in lightly doped Mott insulators
It is widely believed that high-temperature superconductivity in the cuprates
emerges from doped Mott insulators. The physics of the parent state seems
deceivingly simple: The hopping of the electrons from site to site is
prohibited because their on-site Coulomb repulsion U is larger than the kinetic
energy gain t. When doping these materials by inserting a small percentage of
extra carriers, the electrons become mobile but the strong correlations from
the Mott state are thought to survive; inhomogeneous electronic order, a
mysterious pseudogap and, eventually, superconductivity appear. How the
insertion of dopant atoms drives this evolution is not known, nor whether these
phenomena are mere distractions specific to hole-doped cuprates or represent
the genuine physics of doped Mott insulators. Here, we visualize the evolution
of the electronic states of (Sr1-xLax)2IrO4, which is an effective spin-1/2
Mott insulator like the cuprates, but is chemically radically different. Using
spectroscopic-imaging STM, we find that for doping concentration of x=5%, an
inhomogeneous, phase separated state emerges, with the nucleation of pseudogap
puddles around clusters of dopant atoms. Within these puddles, we observe the
same glassy electronic order that is so iconic for the underdoped cuprates.
Further, we illuminate the genesis of this state using the unique possibility
to localize dopant atoms on topographs in these samples. At low doping, we find
evidence for much deeper trapping of carriers compared to the cuprates. This
leads to fully gapped spectra with the chemical potential at mid-gap, which
abruptly collapse at a threshold of around 4%. Our results clarify the melting
of the Mott state, and establish phase separation and electronic order as
generic features of doped Mott insulators.Comment: This version contains the supplementary information and small updates
on figures and tex
Pseudomonas aeruginosa PAO1 Preferentially Grows as Aggregates in Liquid Batch Cultures and Disperses upon Starvation
In both natural and artificial environments, bacteria predominantly grow in biofilms, and bacteria often disperse from biofilms as freely suspended single-cells. In the present study, the formation and dispersal of planktonic cellular aggregates, or ‘suspended biofilms’, by Pseudomonas aeruginosa in liquid batch cultures were closely examined, and compared to biofilm formation on a matrix of polyester (PE) fibers as solid surface in batch cultures. Plankton samples were analyzed by laser-diffraction particle-size scanning (LDA) and microscopy of aggregates. Interestingly, LDA indicated that up to 90% of the total planktonic biomass consisted of cellular aggregates in the size range of 10–400 µm in diameter during the growth phase, as opposed to individual cells. In cultures with PE surfaces, P. aeruginosa preferred to grow in biofilms, as opposed to planktonicly. However, upon carbon, nitrogen or oxygen limitation, the planktonic aggregates and PE-attached biofilms dispersed into single cells, resulting in an increase in optical density (OD) independent of cellular growth. During growth, planktonic aggregates and PE-attached biofilms contained densely packed viable cells and extracellular DNA (eDNA), and starvation resulted in a loss of viable cells, and an increase in dead cells and eDNA. Furthermore, a release of metabolites and infective bacteriophage into the culture supernatant, and a marked decrease in intracellular concentration of the second messenger cyclic di-GMP, was observed in dispersing cultures. Thus, what traditionally has been described as planktonic, individual cell cultures of P. aeruginosa, are in fact suspended biofilms, and such aggregates have behaviors and responses (e.g. dispersal) similar to surface associated biofilms. In addition, we suggest that this planktonic biofilm model system can provide the basis for a detailed analysis of the synchronized biofilm life cycle of P. aeruginosa
How Cooper pairs vanish approaching the Mott insulator in Bi2Sr2CaCu2O8+d
The antiferromagnetic ground state of copper oxide Mott insulators is
achieved by localizing an electron at each copper atom in real space (r-space).
Removing a small fraction of these electrons (hole doping) transforms this
system into a superconducting fluid of delocalized Cooper pairs in momentum
space (k-space). During this transformation, two distinctive classes of
electronic excitations appear. At high energies, the enigmatic 'pseudogap'
excitations are found, whereas, at lower energies, Bogoliubov quasi-particles
-- the excitations resulting from the breaking of Cooper pairs -- should exist.
To explore this transformation, and to identify the two excitation types, we
have imaged the electronic structure of Bi2Sr2CaCu2O8+d in r-space and k-space
simultaneously. We find that although the low energy excitations are indeed
Bogoliubov quasi-particles, they occupy only a restricted region of k-space
that shrinks rapidly with diminishing hole density. Concomitantly, spectral
weight is transferred to higher energy r-space states that lack the
characteristics of excitations from delocalized Cooper pairs. Instead, these
states break translational and rotational symmetries locally at the atomic
scale in an energy independent fashion. We demonstrate that these unusual
r-space excitations are, in fact, the pseudogap states. Thus, as the Mott
insulating state is approached by decreasing the hole density, the delocalized
Cooper pairs vanish from k-space, to be replaced by locally translational- and
rotational-symmetry-breaking pseudogap states in r-space.Comment: This is author's version. See the Nature website for the published
versio
Microbial Activities and Dissolved Organic Matter Dynamics in Oil-Contaminated Surface Seawater from the Deepwater Horizon Oil Spill Site
The Deepwater Horizon oil spill triggered a complex cascade of microbial responses that reshaped the dynamics of heterotrophic carbon degradation and the turnover of dissolved organic carbon (DOC) in oil contaminated waters. Our results from 21-day laboratory incubations in rotating glass bottles (roller bottles) demonstrate that microbial dynamics and carbon flux in oil-contaminated surface water sampled near the spill site two weeks after the onset of the blowout were greatly affected by activities of microbes associated with macroscopic oil aggregates. Roller bottles with oil-amended water showed rapid formation of oil aggregates that were similar in size and appearance compared to oil aggregates observed in surface waters near the spill site. Oil aggregates that formed in roller bottles were densely colonized by heterotrophic bacteria, exhibiting high rates of enzymatic activity (lipase hydrolysis) indicative of oil degradation. Ambient waters surrounding aggregates also showed enhanced microbial activities not directly associated with primary oil-degradation (β-glucosidase; peptidase), as well as a twofold increase in DOC. Concurrent changes in fluorescence properties of colored dissolved organic matter (CDOM) suggest an increase in oil-derived, aromatic hydrocarbons in the DOC pool. Thus our data indicate that oil aggregates mediate, by two distinct mechanisms, the transfer of hydrocarbons to the deep sea: a microbially-derived flux of oil-derived DOC from sinking oil aggregates into the ambient water column, and rapid sedimentation of the oil aggregates themselves, serving as vehicles for oily particulate matter as well as oil aggregate-associated microbial communities
Intra-unit-cell electronic nematicity of the high-Tc copper-oxide pseudogap states
In the high-transition-temperature (high-Tc) superconductors the pseudogap
phase becomes predominant when the density of doped holes is reduced1. Within
this phase it has been unclear which electronic symmetries (if any) are broken,
what the identity of any associated order parameter might be, and which
microscopic electronic degrees of freedom are active. Here we report the
determination of a quantitative order parameter representing intra-unit-cell
nematicity: the breaking of rotational symmetry by the electronic structure
within CuO2 unit cell. We analyze spectroscopic-imaging scanning tunneling
microscope images of the intra-unit-cell states in underdoped
Bi2Sr2CaCu2O8+{\delta} and, using two independent evaluation techniques, find
evidence for electronic nematicity of the states close to the pseudogap energy.
Moreover, we demonstrate directly that these phenomena arise from electronic
differences at the two oxygen sites within each unit cell. If the
characteristics of the pseudogap seen here and by other techniques all have the
same microscopic origin, this phase involves weak magnetic states at the O
sites that break 90o -rotational symmetry within every CuO2 unit cell.Comment: See the Nature website for the published version. High-resolution
version of figures, supplementary information and supplementary movies are
available at http://eunahkim.ccmr.cornell.edu/KimGroup/highlights.htm
Seasonal variations in the nitrogen isotopic composition of settling particles at station K2 in the western subarctic North Pacific
Intensive observations using hydrographical cruises and moored sediment trap deployments during 2010 and 2012 at station K2 in the North Pacific western subarctic gyre (WSG) revealed seasonal changes in δ15N of both suspended and settling particles. Suspended particles (SUS) were collected from depths between the surface and 200 m; settling particles by drifting traps (DST; 100-200 m) and moored traps (MST; 200 and 500 m). All particles showed higher δ15N values in winter and lower in summer, contrary to the expected by isotopic fractionation during phytoplankton nitrate consumption. We suggest that these observed isotopic patterns are due to ammonium consumption via light-controlled nitrification, which could induce variations in δ15N(SUS) of 0.4-3.1 ‰ in the euphotic zone (EZ). The δ15N(SUS) signature was reflected by δ15 N(DST) despite modifications during biogenic transformation from suspended particles in the EZ. δ15 N enrichment (average: 3.6 ‰) and the increase in C:N ratio (by 1.6) in settling particles suggests year-round contributions of metabolites from herbivorous zooplankton as well as TEPs produced by diatoms. Accordingly, seasonal δ15 N(DST) variations of 2.4-7.0 ‰ showed a significant correlation with primary productivity (PP) at K2. By applying the observed δ15 N(DST) vs. PP regression to δ15 N(MST) of 1.9-8.0 ‰, we constructed the first annual time-series of PP changes in the WSG. Moreover, the monthly export ratio at 500 m was calculated using both estimated PP and measured organic carbon fluxes. Results suggest a 1.6 to 1.8 times more efficient transport of photosynthetically-fixed carbon to the intermediate layers occurs in summer/autumn rather than winter/spring
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