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Phase change memory (PCM) is a high speed, high endurance, high density non-volatile memory technology that utilizes chalcogenide materials such as Ge 2 Sb 2 Te 5 (GST) that can be electrically cycled between highly resistive amorphous and low resistance crystalline phases. The resistance of the amorphous phase of PCM cells increase (drift) in time following a power law [1] , which increases the memory window in time but limits in the implementation of multi-bit-per-cell PCM. There has been a number of theories explaining the origin of drift [1] - [4] , mostly attributing it to structural relaxation, a thermally activated rearrangement of atoms in the amorphous structure [2] . Most of the studies on resistance drift are based on experiments at or above room temperature, where multiple processes may be occurring simultaneously. In this work, we melt-quenched amorphized GST line cells with widths ~120-140 nm, lengths ~390-500 nm, and thickness ~50nm ( Fig. 1 ) and monitored the current-voltage (I-V) characteristics using a parameter analyzer ( Fig. 2 ) in 85 K to 350 K range. We extracted the drift co-efficient from the slope of the resistance vs. time plots (using low-voltage measurements) and observed resistance drift in the 125 K -300 K temperature range ( Fig. 3 ). We found an approximately linear increase in drift coefficient as a function of temperature from ~ 0.07 at 125 K to ~ 0.11 at 200 K and approximately constant drift coefficients in the 200 K to 300 K range ( Fig. 3 inset). These results suggest that structural relaxations alone cannot account for resistance drift, additional mechanisms are contributing to this phenomenon [5] , [6] .
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Stopping Resistance Drift in Phase Change Memory Cells and Analysis of Charge Transport in Stable Amorphous Ge2Sb2Te5
We stabilize resistance of melt-quenched amorphous Ge2Sb2Te5 (a-GST) phase change memory (PCM) line cells by substantially accelerating resistance drift and bringing it to a stop within a few minutes with application of high electric field stresses. The acceleration of drift is clearly observable at electric fields > 26 MV/m at all temperatures (85 K - 300 K) and is independent of the current forced through the device, which is a strong function of temperature. The low-field (< 21 MV/m) I-V characteristics of the stabilized cells measured in 85 K - 300 K range fit well to a 2D thermally-activated hopping transport model, yielding hopping distances in the direction of the field and activation energies ranging from 2 nm and 0.2 eV at 85 K to 6 nm and 0.4 eV at 300 K. Hopping transport appears to be better aligned with the field direction at higher temperatures. The high-field current response to voltage is significantly stronger and displays a distinctly different characteristic: the differential resistances at different temperatures extrapolate to a single point (8.9x10-8 this http URL), comparable to the resistivity of copper at 60 K, at 65.6 +/- 0.4 MV/m. The physical mechanisms that give rise to the substantial increase in current in the high-field regime also accelerate resistance drift. We constructed field and temperature dependent conduction models based on the experimental results and integrated it with our electro-thermal finite element device simulation framework to analyze reset, set and read operations of PCM devices.
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- Award ID(s):
- 1711626
- PAR ID:
- 10431631
- Date Published:
- Journal Name:
- arXivorg
- ISSN:
- 2331-8422
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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