Locking Tetrahedral Ge Coordination Enables Stable Multilevel Phase-Change Memory
As data-intensive technologies continue to scale, phase-change random access memory (PCRAM) has emerged as a leading contender for next-generation nonvolatile memory. However, its practical deployment remains hindered by limited storage density and resistance drift. Herein, we report a superlattice-like structure comprising [GeTe(24 nm)/Ge(2 nm)/Ge<sub>2</sub>Sb<sub>2</sub>Te<sub>5</sub>(24 nm)]<sub>1</sub>, where the incorporation of an ultrathin Ge buffer layer promotes the formation of tetrahedral Ge units, effectively suppressing the tetrahedral-to-octahedral ("umbrella-flip") coordination transition in Ge<sub>2</sub>Sb<sub>2</sub>Te<sub>5</sub>, while simultaneously stabilizing the structural evolution of the intermediate-resistance state to ensure reliable multilevel storage. This structural stabilization facilitates a well-defined sequential crystallization pathway, evolving from the amorphous state through an intermediate face-centered cubic (FCC) phase, and finally transitioning into a stable hexagonal (HEX) configuration. These findings highlight the potential of Ge-buffered superlattice-like structures as a robust platform for high-density multilevel memory applications.
Authors
- Ruirui Liu (ORCID: https://orcid.org/0000-0003-3720-347X)
- Huafeng Zhang (ORCID: https://orcid.org/0000-0003-2400-5941)
- Jiwei Zhai
- Yukun Chen
- Sannian Song
- Zhitang Song
- Xiao Zhou
- Dexu Feng
- Ke Liu
- Liu Liu
Institutions
- Tongji University (CN)
- Shanghai Jiao Tong University (CN)
- Chinese Academy of Sciences (CN)
- Metal Matrix Cast Composites (United States) (US)
- Shanghai Institute of Microsystem and Information Technology (CN)
- Shanghai Research Institute of Materials (CN)
- Shanghai Institute of Technology (CN)
Publication Details
- Journal
- ACS Applied Materials & Interfaces
- Published
- 2026-01-13
- DOI
- https://doi.org/10.1021/acsami.5c18011
- Primary Topic
- Phase-change materials and chalcogenides
- Type
- article
- Field-Weighted Citation Impact
- 0.00