Advanced interfacial phase change material: Structurally confined and interfacially extended superlatticeopen access
- Authors
- Lim, Hyeonwook; Kim, Youngsam; Jo, Kyu-Jin; Seok Choi; Lee, Chang Woo; Kim, Dasol; Kwon, Gihyeon; Kwon, Hoedon; Hwang, Soobin; Jeong, Kwangsik; Choi, Byung-Joon; Yang, Cheol-Woong; Sim, Eunji; Cho, Mann-Ho
- Issue Date
- Sep-2023
- Publisher
- Elsevier B.V.
- Keywords
- Doping; Interfacial phase change materials; Neuromorphic; Superlattice; vdW layer
- Citation
- Materials Today, v.68, pp 62 - 73
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Materials Today
- Volume
- 68
- Start Page
- 62
- End Page
- 73
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/21035
- DOI
- 10.1016/j.mattod.2023.07.025
- ISSN
- 1369-7021
1873-4103
- Abstract
- Interfacial Phase Change Memory (iPCM) retrench unnecessary power consumption due to wasted heat generated during phase change by reducing unnecessary entropic loss. In this study, an advanced iPCM (GeTe/Ti-Sb2Te3 Superlattice) is synthesized by doping Ti into Sb2Te3. Structural analysis and density functional theory (DFT) calculations confirm that bonding distortion and structurally well-confined layers contribute to improve phase change properties in iPCM. Ti-Sb2Te3 acts as an effective thermal barrier to localize the generated heat inside active region, which leads to reduction of switching energy. Since Ge-Te bonds adjacent to short and strong Ti-Te bonds are more elongated than the bonds near Sb-Te, it is easier for Ge atoms to break the bond with Te due to strengthened Peierls distortions (Rlong/Rshort) during phase change process. Properties of advanced iPCM (cycling endurance, write speed/energy) exceed previous records. Moreover, well-confined multi-level states are obtained with advanced iPCM, showing potential as a neuromorphic memory. Our work paves the way for designing superlattice based PCM by controlling confinement layers. © 2023 Elsevier Ltd
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Collections - College of Natural Science > Division of Physics & Semiconductor Science > 1. Journal Articles

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