Quantifying redox-induced Schottky barrier variations in memristive devices via in operando spectromicroscopy with graphene electrodes

The continuing revolutionary success of mobile computing and smart devices calls for the development of novel, cost- and energy-efficient memories. Resistive switching is attractive because of, inter alia, increased switching speed and device density. On electrical stimulus, complex nanoscale redox...

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Veröffentlicht in:Nature communications 2016-08, Vol.7 (1), p.12398-12398, Article 12398
Hauptverfasser: Baeumer, Christoph, Schmitz, Christoph, Marchewka, Astrid, Mueller, David N., Valenta, Richard, Hackl, Johanna, Raab, Nicolas, Rogers, Steven P., Khan, M. Imtiaz, Nemsak, Slavomir, Shim, Moonsub, Menzel, Stephan, Schneider, Claus Michael, Waser, Rainer, Dittmann, Regina
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Sprache:eng
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Zusammenfassung:The continuing revolutionary success of mobile computing and smart devices calls for the development of novel, cost- and energy-efficient memories. Resistive switching is attractive because of, inter alia, increased switching speed and device density. On electrical stimulus, complex nanoscale redox processes are suspected to induce a resistance change in memristive devices. Quantitative information about these processes, which has been experimentally inaccessible so far, is essential for further advances. Here we use in operando spectromicroscopy to verify that redox reactions drive the resistance change. A remarkable agreement between experimental quantification of the redox state and device simulation reveals that changes in donor concentration by a factor of 2–3 at electrode-oxide interfaces cause a modulation of the effective Schottky barrier and lead to >2 orders of magnitude change in device resistance. These findings allow realistic device simulations, opening a route to less empirical and more predictive design of future memory cells. Resistive switching in metal oxides is related to the migration of donor defects. Here Baeumer et al. use in operando X-ray spectromicroscopy to quantify the doping locally and show that small local variations in the donor concentration result in large variations in the device resistance.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms12398