Issue 14, 2017

Insight into the role of oxygen in the phase-change material GeTe

Abstract

Oxygen is widely used to tune the performance of chalcogenide phase-change materials in the usage of phase-change random access memory (PCRAM), which is considered as the most promising next-generation non-volatile memory. However, the microscopic role of oxygen in the write–erase process, i.e., the reversible phase transition between crystalline and amorphous state of phase-change materials, remains unclear. Using oxygen doped GeTe as an example, this study unravels the role of oxygen at the atomic scale by means of ab initio total energy calculations and ab initio molecular dynamics simulations. Our main finding is that after the amorphization and the subsequent re-crystallization process simulated by ab initio molecular dynamics, oxygen will drag one Ge atom out of its lattice site and both atoms will stay in the interstitial region near the Te vacancy that was originally occupied by oxygen, forming a “dumbbell-like” defect (O–VTe–Ge), which is in sharp contrast to the results of ab initio total energy calculations at 0 K showing that the oxygen prefers to substitute Te in crystalline GeTe. This specific defect configuration leads to a slower crystallization speed and hence the improved data retention of oxygen doped GeTe. Moreover, we find that the local oxygen configuration will increase the effective mass of the carrier and thus increase the resistivity of GeTe. Our results unravel the microscopic mechanism of the oxygen-doping optimization of GeTe phase-change material, and the present reported mechanism can be applied to other oxygen doped ternary chalcogenide phase-change materials.

Graphical abstract: Insight into the role of oxygen in the phase-change material GeTe

Supplementary files

Article information

Article type
Paper
Submitted
10 Jan 2017
Accepted
13 Mar 2017
First published
14 Mar 2017

J. Mater. Chem. C, 2017,5, 3592-3599

Insight into the role of oxygen in the phase-change material GeTe

L. Zhu, Z. Li, J. Zhou, N. Miao and Z. Sun, J. Mater. Chem. C, 2017, 5, 3592 DOI: 10.1039/C7TC00127D

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