Abstract
The valence change model describes the resistive switching in metal oxide-based devices as due to electroreduction of the oxide and subsequent electromigration of oxygen vacancies. Here, we present cross-sectional X-ray energy-dispersive spectroscopy elemental maps of Ta, O, N, and Ti in electroformed TiN/TaO2.0/TiN structures. O, N, and Ti were exchanged between the anode and the functional oxide in devices formed at high power (∼1 mW), but the exchange was below the detection limit at low power (<0.5 mW). All structures exhibit a similar Ta-enriched and O-depleted filament formed by the elemental segregation in the functional oxide by the temperature gradient. The elemental interchange is interpreted as due to Fick's diffusion caused by high temperatures in the gap of the filament and is not an essential part of electroformation.
Original language | English |
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Pages (from-to) | 27378-27385 |
Number of pages | 8 |
Journal | ACS Applied Materials and Interfaces |
Volume | 12 |
Issue number | 24 |
DOIs | |
State | Published - Jun 17 2020 |
Funding
This work was supported in part by NSF Grant DMR-1905648 and the Data Storage Systems Center at Carnegie Mellon University. The authors acknowledge the use of the Materials Characterization Facility at Carnegie Mellon University supported by grant MCF-677785 and the electron microscopy facilities at Oak Ridge National Laboratory’s Center for Nanophase Materials Sciences, which is a U.S. Department of Energy, Office of Science User Facility.
Funders | Funder number |
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National Science Foundation | DMR-1905648, 1905648 |
U.S. Department of Energy | |
Office of Science | |
Carnegie Mellon University | MCF-677785 |
Keywords
- electroformation
- electroreduction
- interdiffusion
- resistive switching devices
- valence change model