61 research outputs found
Origin of magnetic moments and presence of a resonating valence bond state in BaYIrO
While it was speculated that 5 systems would possess non-magnetic
~=~0 ground state due to strong Spin-Orbit Coupling (SOC), all such systems
have invariably shown presence of magnetic moments so far. A puzzling case is
that of BaYIrO, which in spite of having a perfectly cubic structure
with largely separated Ir () ions, has consistently shown presence
of weak magnetic moments. Moreover, we clearly show from Muon Spin Relaxation
(SR) measurements that a change in the magnetic environment of the
implanted muons in BaYIrO occurs as temperature is lowered below 10~K.
This observation becomes counterintuitive, as the estimated value of SOC
obtained by fitting the RIXS spectrum of BaYIrO with an atomic
model is found to be as high as 0.39~eV, meaning that the system within this
model is neither expected to possess moments nor exhibit temperature dependent
magnetic response. Therefore we argue that the atomic coupling
description is not sufficient to explain the ground state of such systems,
where despite having strong SOC, presence of hopping triggers delocalisation of
holes, resulting in spontaneous generation of magnetic moments. Our theoretical
calculations further indicate that these moments favour formation of
spin-orbital singlets in the case of BaYIrO, which is manifested in
SR experiments measured down to 60~mK.Comment: 20 Pages, 7 Figure
Correlation driven near-flat band Stoner excitations in a Kagome magnet
Among condensed matter systems, Mott insulators exhibit diverse properties
that emerge from electronic correlations. In itinerant metals, correlations are
usually weak, but can also be enhanced via geometrical confinement of
electrons, that manifest as `flat' dispersionless electronic bands. In the fast
developing field of topological materials, which includes Dirac and Weyl
semimetals, flat bands are one of the important components that can result in
unusual magnetic and transport behaviour. To date, characterisation of flat
bands and their magnetism is scarce, hindering the design of novel materials.
Here, we investigate the ferromagnetic Kagom\'{e} semimetal CoSnS
using resonant inelastic X-ray scattering. Remarkably, nearly non-dispersive
Stoner spin excitation peaks are observed, sharply contrasting with the
featureless Stoner continuum expected in conventional ferromagnetic metals. Our
band structure and dynamic spin susceptibility calculations, and thermal
evolution of the excitations, confirm the nearly non-dispersive Stoner
excitations as unique signatures of correlations and spin-polarized electronic
flat bands in CoSnS. These observations serve as a cornerstone for
further exploration of band-induced symmetry-breaking orders in topological
materials.Comment: 15 pages, 4 figures, and Supplementary Informatio
The nature of plasmon excitations in hole-doped cuprate superconductors
High Tc superconductors show a rich variety of phases associated with their
charge degrees of freedom. Valence charges can give rise to charge ordering or
acoustic plasmons in these layered cuprate superconductors. While charge
ordering has been observed for both hole- and electron-doped cuprates, acoustic
plasmons have only been found in electron-doped materials. Here, we use
resonant inelastic X-ray scattering (RIXS) to observe the presence of acoustic
plasmons in two families of hole-doped cuprate superconductors [La2-xSrxCuO4
(LSCO) and Bi2Sr1.6La0.4CuO6+d (Bi2201)], crucially completing the picture.
Interestingly, in contrast to the quasi-static charge ordering which manifests
at both Cu and O sites, the observed acoustic plasmons are predominantly
associated with the O sites, revealing a unique dichotomy in the behaviour of
valence charges in hole-doped cuprates.Comment: 11 pages, 7 figures + Supplementary Informatio
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Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.
Primary open angle glaucoma (POAG) is a complex disease with a major genetic contribution. Its prevalence varies greatly among ethnic groups, and is up to five times more frequent in black African populations compared to Europeans. So far, worldwide efforts to elucidate the genetic complexity of POAG in African populations has been limited. We conducted a genome-wide association study in 1113 POAG cases and 1826 controls from Tanzanian, South African and African American study samples. Apart from confirming evidence of association at TXNRD2 (rs16984299; OR[T] 1.20; P = 0.003), we found that a genetic risk score combining the effects of the 15 previously reported POAG loci was significantly associated with POAG in our samples (OR 1.56; 95% CI 1.26-1.93; P = 4.79 × 10-5). By genome-wide association testing we identified a novel candidate locus, rs141186647, harboring EXOC4 (OR[A] 0.48; P = 3.75 × 10-8), a gene transcribing a component of the exocyst complex involved in vesicle transport. The low frequency and high degree of genetic heterogeneity at this region hampered validation of this finding in predominantly West-African replication sets. Our results suggest that established genetic risk factors play a role in African POAG, however, they do not explain the higher disease load. The high heterogeneity within Africans remains a challenge to identify the genetic commonalities for POAG in this ethnicity, and demands studies of extremely large size
Evolution of spin excitations from bulk to monolayer FeSe
In ultrathin films of FeSe grown on SrTiO (FeSe/STO), the superconducting transition temperature T is increased by almost an order of magnitude, raising questions on the pairing mechanism. As in other superconductors, antiferromagnetic spin fluctuations have been proposed to mediate SC making it essential to study the evolution of the spin dynamics of FeSe from the bulk to the ultrathin limit. Here, we investigate the spin excitations in bulk and monolayer FeSe/STO using resonant inelastic x-ray scattering (RIXS) and quantum Monte Carlo (QMC) calculations. Despite the absence of long-range magnetic order, bulk FeSe displays dispersive magnetic excitations reminiscent of other Fe-pnictides. Conversely, the spin excitations in FeSe/STO are gapped, dispersionless, and significantly hardened relative to its bulk counterpart. By comparing our RIXS results with simulations of a bilayer Hubbard model, we connect the evolution of the spin excitations to the Fermiology of the two systems revealing a remarkable reconfiguration of spin excitations in FeSe/STO, essential to understand the role of spin fluctuations in the pairing mechanism
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Emmanuelle Souzeau, who contributed to analysis of data, was inadvertently omitted from the author list in the originally published version of this Article. This has now been corrected in both the PDF and HTML versions of the Article
Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Recently, the Haplotype Reference Consortium (HRC) released a large imputation panel that allows more accurate imputation of genetic variants. In this study, we compared a set of directly assayed common and rare variants from an exome array to imputed genotypes, that is, 1000 genomes project (1000GP) and HRC. We showed that imputation using the HRC panel improved the concordance between assayed and imputed genotypes at common, and especially, low-frequency variants. Furthermore, we performed a genome-wide association meta-analysis of vertical cup-disc ratio, a highly heritable endophenotype of glaucoma, in four cohorts using 1000GP and HRC imputations. We compared the results of the meta-analysis using 1000GP to the meta-analysis results using HRC. Overall, we found that using HRC imputation significantly improved P values (P = 3.07 × 10-61), particularly for suggestive variants. Both meta-analyses were performed in the same sample size, yet we found eight genome-wide significant loci in the HRC-based meta-analysis versus seven genome-wide significant loci in the 1000GP-based meta-analysis. This study provides supporting evidence of the new avenues for gene discovery and fine mapping that the HRC imputation panel offers
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide association meta-analysis of CCT and identify 19 novel regions. In addition to adding support for known connective tissue-related pathways, pathway analyses uncover previously unreported gene sets. Remarkably, >20% of the CCT-loci are near or within Mendelian disorder genes. These included FBN1, ADAMTS2 and TGFB2 which associate with connective tissue disorders (Marfan, Ehlers-Danlos and Loeys-Dietz syndromes), and the LUM-DCN-KERA gene complex involved in myopia, corneal dystrophies and cornea plana. Using index CCT-increasing variants, we find a significant inverse correlation in effect sizes between CCT and keratoconus (r =-0.62, P = 5.30 × 10-5) but not between CCT and primary open-angle glaucoma (r =-0.17, P = 0.2). Our findings provide evidence for shared genetic influences between CCT and keratoconus, and implicate candidate genes acting in collagen and extracellular matrix regulation
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