AVS 60th International Symposium and Exhibition
    Electronic Materials and Processing Wednesday Sessions
       Session EM+PS-WeM

Paper EM+PS-WeM4
The Effect of High-Pressured N2 Annealing in NiOx based Resistive Random Access Memory

Wednesday, October 30, 2013, 9:00 am, Room 102 A

Session: Oxides and Dielectrics for Novel Devices and Ultra-dense Memory II
Presenter: D.H. Yoon, Yonsei University, Republic of Korea
Authors: D.H. Yoon, Yonsei University, Republic of Korea
Y.J. Tak, Yonsei University, Republic of Korea
J. Jung, Yonsei University, Republic of Korea
S.J. Kim, Yonsei University, Republic of Korea
H.J. Kim, Yonsei University, Republic of Korea
Correspondent: Click to Email

High pressure annealing (HPA) is known as an effective way to control the fundamentals of oxide system through the modification of stoichiometry, thermal decomposition, and compression.[1] Here, we report the effect of N2 HPA on NiOx based resistive random access memory (RRAM) device in terms of applied pressures in NiOx system. In this research, the annealing temperature was fixed at 350 oC while the applied pressures were varied to 1, 20, and 50 atm. Pt was commonly used as bottom and top layer of metal-insulator-metal structure. As the N2 pressure increased, the on- and off- resistance ratio was decreased from ~105 to ~104. However, the operation voltages (reset and set voltage) were reduced followed by increment of N2 pressure. Specifically, the 50 atm HPA sample shows the lowest reset voltage of 0.95 V and set voltage of 2.12 V. This result implies that enhanced grain size was induced by the N2 pressure as the grain boundaries are preference sites for conduction filament formation.[2] Furthermore, notable increment of non-lattice oxide component was confirmed which may cause the reduced driving voltages by x-ray photoelectron spectroscopy. These findings can enhance the understanding of low-power driving RRAM for next generation memory device.

References:

[1] Y. S. Rim, W. H. Jeong, D. L. Kim, H. S. Lim, K. M. Kim and H. J. Kim, J. Mater. Chem. 22, 12491 (2012).

[2] S. Kim, D. Lee, J. Park, S. Jung, W. Lee, J. Shin, G. Choi, and H. Hwang, Nanotech. 23, 325702 (2012).