Affiliation:
1. 1st Institute of Physics (IA) and JARA‐FIT RWTH Aachen University 52074 Aachen Germany
2. Peter Gruenberg Institute – Electronic Materials (PGI‐7) and JARA‐FIT Forschungszentrum Juelich GmbH 52425 Juelich Germany
3. 2nd Institute of Physics and JARA‐FIT RWTH Aachen University 52074 Aachen Germany
Abstract
AbstractResistive switching devices based on metal oxides are candidates for nonvolatile memory storage. They often rely on the valence change mechanism, the field‐induced movement of donor ions leading to nanoscale conductive paths in filamentary‐type devices. Devices usually consist of a transition metal oxide like Ta2O5 sandwiched between two metal electrodes. Critical parameters of the devices, such as cycle‐to‐cycle variability, Roff/Ron ratio, and endurance depend on the morphology and composition of the filaments. However, investigating filaments on the nanoscale is cumbersome, and commonly applied techniques such as conductive atomic force or transmission electron microscopy require delaminating the metal top electrode, inhibiting in operando investigations over many switching cycles. Here, the authors use infrared scattering‐type scanning near‐field optical microscopy (s‐SNOM) to investigate resistive switching in Ta2O5 films with a graphene top electrode in operando and reveal individual filaments on the device level. By selecting an appropriate illumination frequency, the authors can trace the evolution of filaments and the joule heating‐induced retraction of the top electrode until device failure. s‐SNOM promises a deeper understanding of resistive switching devices’ microscopic switching behavior and applies to a wide range of resistive switching oxides, such as HfO2, SrTiO3, and SiO2.
Funder
Deutsche Forschungsgemeinschaft
Cited by
1 articles.
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