arXiv subjects

András Magyarkuti

Publications and source records attributed to András Magyarkuti.

4 recordsLinked to original sources

arXiv2025

Increasing the proximity induced spin-orbit coupling in bilayer graphene/WSe$_2$ heterostructures with pressure

Combining graphene with transition metal dichalcogenides (TMDs) leads to enhanced spin-orbit coupling (SOC) in the graphene. The induced SOC has a large effect on the low-energy part of the band structure leading to or stabilizing novel phases such as topological phases or superconductivity. Here, the pressure dependence of the SOC strength is investigated in bilayer graphene/WSe$_2$ heterostructures. We performed magnetoconductance studies, such as weak localization, quantum Hall, and Shubnikov-de Haas oscillation measurements to extract the different SOC terms which determine the low-energy band structure of BLG. We find the proximity-induced SOC strengths increased by more than 50\% as a result of applying 2\,GPa hydrostatic pressure. Our studies highlight the opportunity to increase the SOC coupling strength with pressure, which can be important for correlated phases or spin qubits in BLG/WSe$_2$ heterostructures.

cond-mat.mes-hall↗

arXiv2023

Configuration-specific insight to single-molecule conductance and noise data revealed by principal component projection method

We explore the merits of neural network boosted, principal-component-projection-based, unsupervised data classification in single-molecule break junction measurements, demonstrating that this method identifies highly relevant trace classes according to the well-defined and well-visualized internal correlations of the dataset. To this end, we investigate single-molecule structures exhibiting double molecular configurations, exploring the role of the leading principal components in the identification of alternative junction evolution trajectories. We show how the proper principal component projections can be applied to separately analyze the high or low-conductance molecular configurations, which we exploit in $1/f$-type noise measurements on bipyridine molecules. This approach untangles the unclear noise evolution of the entire dataset, identifying the coupling of the aromatic ring to the electrodes through the $π$ orbitals in two distinct conductance regions, and its subsequent uncoupling as these configurations are stretched.

cond-mat.mes-hall↗

arXiv2021

1/f noise spectroscopy and noise tailoring of nanoelectronic devices

In this paper, we review the 1/f-type noise properties of nanoelectronic devices focusing on three demonstrative platforms: resistive switching memories, graphene nanogaps and single-molecule nanowires. The functionality of such ultrasmall devices is confined to an extremely small volume, where bulk considerations on the noise loose their validity: the relative contribution of a fluctuator heavily depends on its distance from the device bottleneck, and the noise characteristics are sensitive to the nanometer-scale device geometry and the details of the mostly non-classical transport mechanism. All these are reflected by a highly system-specific dependence of the noise properties on the active device volume (and the related device resitance), the frequency, or the applied voltage. Accordingly, 1/f-type noise measurements serve as a rich fingerprint of the relevant transport and noise-generating mechanisms in the studied nanoelectronic systems. Finally, we demonstrate that not only the fundamental understanding and the targeted noise suppression is fueled by the 1/f-type noise analysis, but novel probabilistic computing hardware platforms heavily seek well tailorable nanoelectric noise sources.

cond-mat.mes-hall↗

arXiv2020

Voltage-controlled binary conductance switching in gold-4,4'-bipyridine-gold single-molecule nanowires

We investigate gold-4,4'-bipyridine-gold single-molecule junctions with the mechanically controllable break junction technique at cryogenic temperature ($T=4.2\,\text{K}$). We observe bistable probabilistic conductance switching between the two molecular binding configurations, influenced both by the mechanical actuation, and the applied voltage. We demonstrate that the relative dominance of the two conductance states is tunable by the electrode displacement, whereas the voltage manipulation induces an exponential speedup of both switching times. The detailed investigation of the voltage-tunable switching rates provides an insight into the possible switching mechanisms.

cond-mat.mes-hall↗