Publications by authors named "Matthew D Watson"

Crystalline solids can become band insulators due to fully filled bands, or Mott insulators due to strong electronic correlations. While Mott insulators can theoretically occur in systems with an even number of electrons per unit cell, distinguishing them from band insulators experimentally has remained a longstanding challenge. In this work, we present a unique momentum-resolved signature of a dimerized Mott-insulating phase in the experimental spectral function of NbBr: the top of the highest occupied band along the out-of-plane direction k has a momentum-space separation Δk = 2π/d, whereas that of a band insulator is less than π/d, where d is the average interlayer spacing.

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Raman microscopy offers a unique combination of chemical and spatial resolution with structural sensitivity. This makes it an ideal tool for studies of protein structural changes in heterogenous samples such as protein liquid-liquid phase separation (LLPS) and amyloid formation. These processes are characterized by the spontaneous assembly of proteins to form either microscopic liquid droplets or insoluble filaments stabilized by β-sheets.

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Tunable quantum materials hold great potential for applications. Of special interest are materials in which small lattice strain induces giant electronic responses. The kagome compounds AVSb (A = K, Rb, Cs) provide a testbed for electronic tunable states.

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Interaction between electrons and phonons in solids is a key effect defining the physical properties of materials, such as electrical and thermal conductivity. In transition metal dichalcogenides (TMDCs), the electron-phonon coupling results in the formation of polarons, quasiparticles that manifest themselves as discrete features in the electronic spectral function. In this study, we report the formation of polarons at the alkali-dosed MoSe surface, where Rashba-like spin splitting of the conduction band states is caused by an inversion-symmetry breaking electric field.

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Doping of a Mott insulator gives rise to a wide variety of exotic emergent states, from high-temperature superconductivity to charge, spin, and orbital orders. The physics underpinning their evolution is, however, poorly understood. A major challenge is the chemical complexity associated with traditional routes to doping.

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Article Synopsis
  • * A photoemission and density-functional theory study was conducted on three compounds to explore how different intercalant elements affect their electronic structures at both the bulk and surface levels.
  • * Findings reveal that as the atomic number of the intercalant increases, there’s greater hybridization with NbS-derived conduction states, resulting in the formation of new electronic states at the Fermi level, which explains previously observed anomalous states and sheds light on tuning magnetic interactions.
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The magnetic skyrmions generated in a centrosymmetric crystal were recently first discovered in Gd_{2}PdSi_{3}. In light of this, we observe the electronic structure by angle-resolved photoemission spectroscopy and unveil its direct relationship with the magnetism in this compound. The Fermi surface and band dispersions are demonstrated to have a good agreement with the density functional theory calculations carried out with careful consideration of the crystal superstructure.

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Spin-orbit coupling in noncentrosymmetric crystals leads to spin-momentum locking - a directional relationship between an electron's spin angular momentum and its linear momentum. Isotropic orthogonal Rashba spin-momentum locking has been studied for decades, while its counterpart, isotropic parallel Weyl spin-momentum locking has remained elusive in experiments. Theory predicts that Weyl spin-momentum locking can only be realized in structurally chiral cubic crystals in the vicinity of Kramers-Weyl or multifold fermions.

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Closing the band gap of a semiconductor into a semimetallic state gives a powerful potential route to tune the electronic energy gains that drive collective phases like charge density waves (CDWs) and excitonic insulator states. We explore this approach for the controversial CDW material monolayer (ML) TiSe by engineering its narrow band gap to the semimetallic limit of ML-TiTe. Using molecular beam epitaxy, we demonstrate the growth of ML-TiTeSe alloys across the entire compositional range and unveil how the (2 × 2) CDW instability evolves through the normal state semiconductor-semimetal transition via angle-resolved photoemission spectroscopy.

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Engineering surfaces and interfaces of materials promises great potential in the field of heterostructures and quantum matter designers, with the opportunity to drive new many-body phases that are absent in the bulk compounds. Here, we focus on the magnetic Weyl kagome system CoSnS and show how for the terminations of different samples the Weyl points connect differently, still preserving the bulk-boundary correspondence. Scanning tunneling microscopy has suggested such a scenario indirectly, and here, we probe the Fermiology of CoSnS directly, by linking it to its real space surface distribution.

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The currently established electronic phase diagram of cuprates is based on a study of single- and double-layered compounds. These CuO planes, however, are directly contacted with dopant layers, thus inevitably disordered with an inhomogeneous electronic state. Here, we solve this issue by investigating a 6-layered BaCaCuO(F,O) with inner CuO layers, which are clean with the extremely low disorder, by angle-resolved photoemission spectroscopy (ARPES) and quantum oscillation measurements.

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Charge Density Waves (CDW) are commonly associated with the presence of near-Fermi level states which are separated from others, or "nested", by a wavector of q. Here we use Angle-Resolved Photo Emission Spectroscopy (ARPES) on the CDW material TaNiSe and identify a total absence of any plausible nesting of states at the primary CDW wavevector q. Nevertheless we observe spectral intensity on replicas of the hole-like valence bands, shifted by a wavevector of q, which appears with the CDW transition.

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Diverse emergent correlated electron phenomena have been observed in twisted-graphene layers. Many electronic structure predictions have been reported exploring this new field, but with few momentum-resolved electronic structure measurements to test them. We use angle-resolved photoemission spectroscopy to study the twist-dependent (1° < θ < 8°) band structure of twisted-bilayer, monolayer-on-bilayer, and double-bilayer graphene (tDBG).

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We report the evolution of the electronic structure at the surface of the layered perovskite Sr_{2}RuO_{4} under large in-plane uniaxial compression, leading to anisotropic B_{1g} strains of ϵ_{xx}-ϵ_{yy}=-0.9±0.1%.

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The integration of metallic contacts with two-dimensional (2D) semiconductors is routinely required for the fabrication of nanoscale devices. However, nanometer-scale variations in the 2D/metal interface can drastically alter the local optoelectronic properties. Here, we map local excitonic changes of the 2D semiconductor MoS in contact with Au.

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α-Synuclein (α-syn) is an intrinsically disordered protein involved in a group of diseases collectively termed synucleinopathies, characterized by the aggregation of α-syn to form insoluble, β-sheet-rich amyloid fibrils. Amyloid fibrils are thought to contribute to disease progression through cell-to-cell transmission, templating and propagating intracellular amyloid formation. Raman spectral imaging offers a direct characterization of protein secondary structure via the amide-I backbone vibration; however, specific detection of α-syn conformational changes against the background of other cellular components presents a challenge.

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: Measurements of the concentric hamstrings-quadriceps strength ratio (Hc:Qc) are almost exclusively recorded in the upright, seated position (hip flexion 80-100°) on an isokinetic dynamometer at angular velocities ranging from 30°/s to 360°/s. Further, there is a scarcity of data examining Hc:Qc ratio in females. : To compare the effects of hip-flexion position (0°, 45°, and 90°) and isokinetic velocity (60°/s, 180°/s, and 300°/s) on knee-extension and knee-flexion torques and the Hc:Qc ratio of females.

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Amyloid diseases are characterized by the aggregation of various proteins to form insoluble β-sheet-rich fibrils leading to cell death. Vibrational spectroscopies have emerged as attractive methods to study this process because of the rich structural information that can be extracted without large, perturbative probes. Importantly, specific vibrations such as the amide-I band directly report on secondary structure changes, which are key features of amyloid formation.

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Globally, people 65 years of age and older are the fastest growing segment of the population. Physiological manifestations of the aging process include undesirable changes in body composition, declines in cardiorespiratory fitness, and reductions in skeletal muscle size and function (i.e.

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Parkinson's disease is characterized by the intracellular accumulation of α-synuclein (α-syn) amyloid fibrils, which are insoluble, β-sheet-rich protein aggregates. Raman spectroscopy is a powerful technique that reports on intrinsic molecular vibrations such as the coupled vibrational modes of the polypeptide backbone, yielding secondary structural information. However, in order to apply this method in cells, spectroscopically unique frequencies are necessary to resolve proteins of interest from the cellular proteome.

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Article Synopsis
  • The study evaluated the reliability and validity of a new Isokinetic Knee Dynamometer against the Biodex System 4 for measuring knee extension and flexion.
  • Thirty-five healthy participants completed tests on both devices, with randomization in order and speed of testing.
  • Results showed the new dynamometer had strong reliability and valid measurements, suggesting it could be more practical and cost-effective for clinical use in assessing knee strength.
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An increasing number of human diseases has been shown to be linked to aggregation and amyloid formation by intrinsically disordered proteins (IDPs). Amylin, amyloid-β, and α-synuclein are, indeed, involved in type-II diabetes, Alzheimer's, and Parkinson's, respectively. Despite the correlation of the toxicity of these proteins at early aggregation stages with membrane damage, the molecular events underlying the process is quite complex to understand.

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Article Synopsis
  • The SSASP test shows a strong correlation with isokinetic shoulder flexion and elbow extension strength, suggesting it effectively measures upper-extremity strength.
  • There was a significant bias in the limb symmetry indices (LSI) for shoulder strength but not for elbow strength, indicating discrepancies in measuring symmetry between the two types of tests.
  • The findings highlight that while the SSASP test represents contributions from both shoulder and elbow, the variability in LSI results suggests that it may not consistently reflect true strength balance between the two.
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Objectives: To compare kinematic and ground reaction force (GRF) patterns between the dominant and non-dominant limbs in males and females conducting the closed kinetic chain upper extremity stability test (CKCUEST).

Design: Descriptive.

Setting: Biomechanics laboratory.

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