Publications by authors named "Klara Volckaert"

The dispersion of topological surface bands in MnBiTe-based magnetic topological insulator heterostructures is strongly affected by band hybridization and is spatially inhomogeneous due to varying surface layer terminations on microscopic length scales. Here, we apply micro-focused angle-resolved photoemission spectroscopy with tunable photon energy from 18 to 30 eV to distinguish bulk valence and conduction bands from surface bands on the three surface terminations of MnBiTe. We observe a strong enhancement of photoemission intensity from the topological surface bands at the Bi Oabsorption edge, which is exploited to visualize a gapless Dirac cone on the MnBiTe-terminated surface and varying degrees of hybridization effects in the surface bands on the two distinct BiTe-terminated surfaces.

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Angle-resolved photoemission spectroscopy (ARPES) with spatial resolution is emerging as a powerful investigative tool for the study of operational mesoscale devices and quantum materials. Here, we introduce AU-SGM4, an extreme ultraviolet beamline based at the ASTRID2 synchrotron, which is designed around an achromatic elliptical capillary optic that focuses the synchrotron light down to a lateral beam spot size of 4 μm. The beamline offers a low photon energy range of 12-150 eV, ideal for probing detailed energy- and momentum-resolved electronic structures of materials.

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Modification of the electronic structure of quantum matter by ad atom deposition allows for directed fundamental design of electronic and magnetic properties. This concept is utilized in the present study in order to tune the surface electronic structure of magnetic topological insulators based on MnBi Te . The topological bands of these systems are typically strongly electron-doped and hybridized with a manifold of surface states that place the salient topological states out of reach of electron transport and practical applications.

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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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Heterostructures composed of the intrinsic magnetic topological insulator MnBiTe and its nonmagnetic counterpart BiTe host distinct surface electronic band structures depending on the stacking order and exposed termination. Here, we probe the ultrafast dynamical response of MnBiTe and MnBiTe following near-infrared optical excitation using time- and angle-resolved photoemission spectroscopy and disentangle surface from bulk dynamics based on density functional theory slab calculations of the surface-projected electronic structure. We gain access to the out-of-equilibrium charge carrier populations of both MnBiTe and BiTe surface terminations of MnBiTe, revealing an instantaneous occupation of states associated with the BiTe surface layer followed by carrier extraction into the adjacent MnBiTe layers with a laser fluence-tunable delay of up to 350 fs.

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The bulk band structure of the topological insulator SbTe is investigated by angle-resolved photoemission spectroscopy. Of particular interest is the dispersion of the uppermost valence band with respect to the topological surface state Dirac point. The valence band maximum has been calculated to be either near the Brillouin zone centre or in a low-symmetry position in the - azimuthal direction.

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To pinpoint the electronic and structural mechanisms that affect intrinsic and extrinsic performance limits of 2D material devices, it is of critical importance to resolve the electronic properties on the mesoscopic length scale of such devices under operating conditions. Herein, angle-resolved photoemission spectroscopy with nanoscale spatial resolution (nanoARPES) is used to map the quasiparticle electronic structure of a twisted bilayer graphene device. The dispersion and linewidth of the Dirac cones associated with top and bottom graphene layers are determined as a function of spatial position on the device under both static and operating conditions.

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The transition-metal dichalcogenide VSe exhibits an increased charge density wave transition temperature and an emerging insulating phase when thinned to a single layer. Here, we investigate the interplay of electronic and lattice degrees of freedom that underpin these phases in single-layer VSe using ultrafast pump-probe photoemission spectroscopy. In the insulating state, we observe a light-induced closure of the energy gap, which we disentangle from the ensuing hot carrier dynamics by fitting a model spectral function to the time-dependent photoemission intensity.

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The presence of an electrical transport current in a material is one of the simplest and most important realizations of nonequilibrium physics. The current density breaks the crystalline symmetry and can give rise to dramatic phenomena, such as sliding charge density waves, insulator-to-metal transitions, or gap openings in topologically protected states. Almost nothing is known about how a current influences the electron spectral function, which characterizes most of the solid's electronic, optical, and chemical properties.

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The possibility of triggering correlated phenomena by placing a singularity of the density of states near the Fermi energy remains an intriguing avenue toward engineering the properties of quantum materials. Twisted bilayer graphene is a key material in this regard because the superlattice produced by the rotated graphene layers introduces a van Hove singularity and flat bands near the Fermi energy that cause the emergence of numerous correlated phases, including superconductivity. Direct demonstration of electrostatic control of the superlattice bands over a wide energy range has, so far, been critically missing.

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Electronic screening can have direct consequences for structural arrangements on the nanoscale, such as on the periodic ordering of adatoms on a surface. So far, such ordering phenomena have been explained in terms of isotropic screening of free electronlike systems. Here, we directly illustrate the structural consequences of anisotropic screening, making use of a highly anisotropic two-dimensional electron gas (2DEG) near the surface of black phosphorous.

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Reliable methods to individually track large numbers of cells in real time are urgently needed to advance our understanding of important biological processes like cancer metastasis, neuronal network development and wound healing. It has recently been suggested to introduce microscopic whispering gallery mode lasers into the cytoplasm of cells and to use their characteristic, size-dependent emission spectrum as optical barcode but so far there is no evidence that this approach is generally applicable. Here, we describe a method that drastically improves intracellular delivery of resonators for several cell types, including mitotic and non-phagocytic cells.

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