Electrical nanopatterning of TiO2 single crystal surfaces in situ via local resistance and potential switching
Source abstract
Abstract
The resistive switching effect in transition metal oxides allows for a dedicated manipulation of the oxide resistance via electrical stimuli. Here, we perform local-conductivity atomic force microscopy simultaneously with the Kelvin probe force microscopy under ultra-high vacuum conditions using the very same tip investigating the very same sample area to monitor the surface conductivity and surface potential of thermally reduced TiO2 single crystals. We show that the resistance of confined surface areas can be switched by applying a voltage of several volts to the tip during scanning in the contact mode. By conducting in situ oxidation experiments, we present that this surface switching is related to a local redox reaction, which can be controlled electrically allowing for surface nanopatterning and illustrates the capability of transition metal oxides for multilevel resistive switching being a prerequisite for neuromorphic computing. We discuss that the features of the electrically engraved nanopattern can be scaled down to a lower boundary at several tens of nanometers. The observed limit around 25 nm is determined by the presence of intrinsic local variations in electrical surface properties appearing as a common phenomenon of slightly reduced metal oxide surfaces.
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Research context
OpenAlex topics: Advanced Memory and Neural Computing · Neuroscience and Neural Engineering · Ferroelectric and Negative Capacitance Devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Forschungszentrum Jülich GmbH, Peter Grünberg Institute (PGI-7), JARA-FIT 1 , 52425 Jülich, Germany
M. Smoluchowski Institute of Physics, Jagiellonian University 2 , 30-348 Krakow, Poland
Department of Solid State Physics, University of Lodz 3 , 90-236 Lodz, Poland
A. Chełkowski Institute of Physics, University of Silesia 4 , 40-007 Katowice, Poland
Funding
Deutsche Forschungsgemeinschaft · Narodowe Centrum Nauki
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