arXiv subjects

Hermann Osterhage

Publications and source records attributed to Hermann Osterhage.

4 recordsLinked to original sources

arXiv2026

A miniature evaporator for in-operando deposition of isolated atoms in a low-temperature scanning tunneling microscope

Depositing dilute atomic ensembles onto cold samples is challenging in low-temperature scanning tunneling microscopes (STM) because radiation shields and restricted internal geometries often preclude a direct deposition path, particularly in instruments designed for millikelvin operation. We present a compact, milliwatt-range evaporation source fabricated from a commercial miniature incandescent lamp and integrated directly into a millikelvin STM head. The exposed tungsten filament is coated with a micrometre-thick Fe film and positioned about 1 cm from the sample. We deposit isolated Fe atoms onto MgO/Ag(100) while operating the microscope near 5 K. Evaporation increases the STM-body temperature by only about 2 K, and the same nanoscopic surface region can be readily scanned after deposition with a lateral displacement of less than 5 nm. Differential-conductance spectra displaying symmetric inelastic steps near $\pm$14 mV identify the deposited atoms on MgO as Fe. From STM images, we estimate a local deposition flux of $1.5\times10^{-5}~\mathrm{nm^{-2}\,s^{-1}}$, corresponding to a nominal evaporator lifetime of ~150 h. The fixed evaporator enables repeated low-flux deposition without a room-temperature line of sight, the need for movable radiation shields, or mechanical evaporator access after cooldown, while preserving access to the same atomic-scale surface region before and after deposition.

cond-mat.mes-hall↗

arXiv2026

Spin-orbit coupling by design in quantum state engineering of atomically defined quantum dots

Tuning spin-orbit coupling is essential in controlling both spin and charge in confined semiconductor nanostructures, yet it is rarely a truly controllable parameter. Here, we show control over the spin-orbit Hamiltonian in quantum dots and the resulting quantum states by tailoring the confinement potential with atomic-scale precision. Using scanning tunnelling microscopy and spectroscopy, we pattern individual Cs ions into designer quantum dot structures on the surface of indium antimonide, in which electrons from a two-dimensional electron gas are confined with chosen in-plane electric-field gradients. We then quantify the atomic level structure, both spatially resolving the orbital character of the electronic states and their magnetic-field evolution. We demonstrate that the level structure, including the induced zero-field splitting, can be tailored by the designed geometry of the local electric fields. These effects can be described using a Hamiltonian that allows consistent treatment of the confinement-induced spin-orbit coupling beyond the conventional Bychkov-Rashba description. This Hamiltonian is derived from a multiband k.p model and takes the energy dependence of the relevant physical parameters into account. Such precise control of spin-orbit coupling in semiconductor quantum dots is relevant to quantum and spintronic technologies.

cond-mat.mes-hall↗

arXiv2024

Quantifying the quantum nature of high spin YSR excitations in transverse magnetic field

Excitations of individual and coupled spins on superconductors provide a platform to study quantum spin impurity models as well as a pathway toward realizing topological quantum computing. Here, we characterize, using ultra-low temperature scanning tunneling microscopy/spectroscopy, the Yu-Shiba-Rusinov (YSR) states of individual manganese phthalocyanine molecules with high spin character on the surface of an ultra-thin lead film in variable transverse magnetic field. We observe two types of YSR excitations, depending on the adsorption geometry of the molecule. Using a zero-bandwidth model, we detail the role of the magnetic anisotropy, spin-spin exchange, and Kondo exchange. We illustrate that one molecular type can be treated as an individual spin akin to an isolated spin on the metal center, whereas the other molecular type invokes a coupled spin system represented by a spin on the center and the ligand. Using the field-dependent evolution of the YSR excitations and comparisons to modeling, we describe the quantum phase of each of the molecules. These results provide an insight into the quantum nature of YSR excitations in magnetic field, and a platform to study spin impurity models on superconductors in magnetic field.

cond-mat.supr-con↗

arXiv2023

Stochastic syncing in sinusoidally driven atomic orbital memory

Stochastically fluctuating multi-well systems as physical implementations of energy-based machine learning models promise a route towards neuromorphic hardware. Understanding the response of multi-well systems to dynamic input signals is crucial in this regard. Here, we investigate the stochastic response of binary orbital memory states derived from individual Fe and Co atoms on a black phosphorus surface to sinusoidal input voltages. Using scanning tunneling microscopy, we quantify the state residence times for DC and AC voltage drive with various input frequencies. We find that Fe and Co atoms both exhibit features of synchronization to the AC input, but only Fe atoms demonstrate a significant frequency-dependent change in the time-averaged state occupations. By modeling the underlying stochastic process, we show that the frequency response of the system is directly related to the DC voltage dependence of the state asymmetry. This relation provides a tunable way to induce population changes in stochastic systems and lays the foundation for understanding the response of multi-well systems to dynamical input signals.

cond-mat.mes-hall↗