journal article·2011-09-01Open access

Redox-controlled memristive switching in the junctions employing Ti reactive electrodes

Haitao Li, Yidong Xia, Hanni Xu, Lifei Liu, Xuefei Li, Zhenjie Tang, Xiangzhong Chen, Aidong Li, Jiang Yin, Zhiguo Liu

AIP Advances· Volume 1· Issue 3

Abstract

We have proposed a kind of memristive device based on the junctions employing Ti as the reactive electrodes. The role of electrically-derived redox of Ti in such memristive switching is shown. The structural and chemical evidence of the electrically-derived oxidation is presented by TEM and XPS experiment, respectively. Due to the redox of the top electrode Ti and the consequent drift of oxygen vacancies, the device shows two distinct resistance states under a sweeping voltage loading. ON state is controlled by tunneling process, while OFF state is controlled by Schottky emission conductive mechanism. The failure behaviors of such memristive junctions are also discussed. In the light of the redox principle, we demonstrate that the devices could be recovered by loading a long electrical reduction treatment.
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Research context

OpenAlex topics: Advanced Memory and Neural Computing · Neuroscience and Neural Engineering · Photoreceptor and optogenetics research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Nanjing University 1 Department of Materials Science and Engineering, , Nanjing 210093, China

Nanjing University 2 National Laboratory of Solid State Microstructures, , Nanjing 210093, China

Nanjing University 3 Department of Polymer Science & Engineering, School of Chemistry & Chemical Engineering, , Nanjing 210093, China

Funding

National Natural Science Foundation of China

References (32)

Show source-provided references
1. 1997
2. Phys. Rev. Lett. · 1997 · 79 · 374410.1103/PhysRevLett.79.3744 ↗
3. Phys. Rev. Lett. · 1998 · 80 · 294110.1103/PhysRevLett.80.2941 ↗
4. Magn. Mater. · 1995 · 139 · L23110.1016/0304-8853(95)90001-2 ↗
5. Materials Today · 2006 · 9 · 3610.1016/S1369-7021(06)71693-5 ↗
6. Nature · 2008 · 453 · 8010.1038/nature06932 ↗
7. Nature Nanotechnology · 2008 · 3 · 42910.1038/nnano.2008.160 ↗
8. IEEE Trans. Circuit Theory · 1971 · 18 · 50710.1109/TCT.1971.1083337 ↗
9. Proc. IEEE · 1976 · 64 · 20910.1109/PROC.1976.10092 ↗
10. Proc. IEEE · 2009 · 97 · 171710.1109/JPROC.2009.2021077 ↗
11. Nano Lett. · 2010 · 10 · 129710.1021/nl904092h ↗
12. Adv. Mater. · 2010 · 22 · 183110.1002/adma.200903680 ↗
13. Appl. Phys. Lett. · 2010 · 97 · 01290210.1063/1.3462067 ↗
14. Adv, Mater. · 2010 · 22 · 403410.1002/adma.201000663 ↗
15. Adv. Mater. · 2009 · 21 · 263210.1002/adma.200900375 ↗
16. Nature · 2005 · 433 · 4710.1038/nature03190 ↗
17. IEEE Trans. Nanotechnol. · 2005 · 4 · 33110.1109/TNANO.2005.846936 ↗
18. Appl. Phys. Lett. · 2009 · 94 · 16211210.1063/1.3123251 ↗
19. J. Appl. Phys. · 2001 · 89 · 524310.1063/1.1361065 ↗
20. Nature Nanotechnology · 2010 · 5 · 14810.1038/nnano.2009.456 ↗
21. Adv. Mater. · 2010 · 22 · 357310.1002/adma.201000186 ↗
22. J. Vac. Sci. Technol. B · 2011 · 29 · 01AD0210.1116/1.3536524 ↗
23. Nano Lett. · 2009 · 9 · 147610.1021/nl803387q ↗
24. Adv. Mater. · 2008 · 20 · 115410.1002/adma.200702024 ↗
25. Appl. Phys. Lett. · 2010 · 96 · 18290410.1063/1.3425671 ↗
26. Nanotechnology · 2009 · 20 · 215209
27. Electrochem. Solid-State Lett. · 2009 · 12 · G3110.1149/1.3122742 ↗
28. J. The Electrochem. Soc. · 2007 · 154 · G18910.1149/1.2750450 ↗
29. Appl. Phys. Lett. · 2011 · 98 · 09350310.1063/1.3560257 ↗
30. 2000
31. Appl. Phys. Lett. · 2010 · 96 · 19211310.1063/1.3428365 ↗
32. 2007