arXiv subjects

D. Wegner

Publications and source records attributed to D. Wegner.

7 recordsLinked to original sources

arXiv2024

Dynamic heterogeneity in the self-induced spin glass state of elemental neodymium

Spin glasses are magnetic materials exhibiting numerous magnetization patterns, that randomly vary both in real space and in time. To date, it is still not well understood what the nature of these spatiotemporal dynamics is, namely if they are completely random or if there are links between given time and length scales. Here we show the ubiquitous behavior of dynamic heterogeneity in the self-induced spin glass state of elemental neodymium. We used spin-polarized scanning tunneling microscopy in combination with atomistic spin dynamics simulations to image the locally ordered magnetic patterns in the glass state, and tracked the induced spatiotemporal dynamics in response to external perturbations. We observed that the real space magnetization exhibited a coexistence of slow and fast dynamics reminiscent of dynamic heterogeneity in structural glasses. Furthermore, we found that zero-field cooling imprints a specific set of metastable periodicities into the spin glass, which evolved during aging and could be thermally reinitialized. These results demonstrate the importance of local length scales for the understanding of aging dynamics in spin glasses and provide a link to the more general picture of true glasses.

cond-mat.mtrl-sci↗

arXiv2022

Quantum simulator to emulate lower dimensional molecular structure

Bottom-up quantum simulators have been developed to quantify the role of various interactions, dimensionality, and structure in creating electronic states of matter. Here, we demonstrated a solid-state quantum simulator emulating molecular orbitals, based solely on positioning individual cesium atoms on an indium antimonide surface. Using scanning tunneling microscopy and spectroscopy, combined with ab initio calculations, we showed that artificial atoms could be made from localized states created from patterned cesium rings. These artificial atoms served as building blocks to realize artificial molecular structures with different orbital symmetries. These corresponding molecular orbitals allowed us to simulate 2D structures reminiscent of well known organic molecules. This platform could further be used to monitor the interplay between atomic structures and the resulting molecular orbital landscape with sub-molecular precision.

cond-mat.mes-hall↗

arXiv2019

p-band engineering in artificial electronic lattices

Artificial electronic lattices, created atom by atom in a scanning tunneling microscope, have emerged as a highly tunable platform to realize and characterize the lowest-energy bands of novel lattice geometries. Here, we show that artificial electronic lattices can be tailored to exhibit higher-energy bands. We study p-like bands in four-fold and three-fold rotationally symmetric lattices. In addition, we show how an anisotropic design can be used to lift the degeneracy between p_x- and p_y-like bands. The experimental measurements are corroborated by muffin-tin and tight-binding calculations. The approach to engineer higher-energy electronic bands in artificial quantum systems introduced here enables the realization of complex band structures from the bottom up.

cond-mat.mes-hall↗

arXiv2007

Effects of impurities on Tamm-like lanthanide-metal surface states

The effects of isolated residual-gas adsorbates on the local electronic structure of the Dy(0001) surface were spatially mapped by scanning tunneling microscopy and spectroscopy at 12 K. Less than 15 A away from an adsorbate, a strong reduction of the intensity and a significant increase of the width of the majority component of the surface state due to impurity scattering were observed, with essentially no change of the minority component; this reflects a high lateral localization of the Tamm-like surface state. Furthermore, an adsorbate-induced state was found that behaves metastable.

cond-mat.mtrl-sci↗

arXiv2005

Surface-electronic structure of La(0001) and Lu(0001)

Most spectroscopic methods for studying the electronic structure of metal surfaces have the disadvantage that either only occupied or only unoccupied states can be probed, and the signal is cut at the Fermi edge. This leads to significant uncertainties, when states are very close to the Fermi level. By performing low-temperature scanning tunneling spectroscopy and ab initio calculations, we study the surface-electronic structure of La(0001) and Lu(0001), and demonstrate that in this way detailed information on the surface-electronic structure very close to the Fermi energy can be derived with high accuracy.

cond-mat.mtrl-sci↗

arXiv2005

Lifetime Widths of Surface States on Magnetic Lanthanide Metals

Low-temperature scanning tunneling spectroscopy is used to study electronic structure and dynamics of d-like surface states of trivalent lanthanide metals from La to Lu. The magnetic exchange splitting of these states is found to scale with the 4f spin multiplied by an effective exchange-coupling constant that increases with 4f occupancy in an approximately linear way. The dynamics of the surfaces states, as revealed by the lifetime width, is dominated by electron-phonon scattering in the occupied region and by electron-magnon scattering in the unoccupied region, respectively.

cond-mat.other↗

arXiv2005

Electronic Structure and Dynamics of Quantum-Well States in thin Yb-Metal Films

Quantum-well states above the Fermi energy in thin Yb(111)-metal films deposited on a W(110) single crystal were studied by low-temperature scanning tunneling spectroscopy. These states are laterally highly localized and give rise to sharp peaks in the tunneling spectra. A quantitative analysis of the spectra yields the bulk-band dispersion in Gamma - L direction as well as quasi-particle lifetimes. The quadratic energy dependence of the lifetimes is in quantitative agreement with Fermi-liquid theory.

cond-mat.other↗