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Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte
Electrochemical metallization (ECM) cell kinetics are strongly determined by the electrolyte and can hardly be altered after the cell has been fabricated. Solid-state property tunable electrolytes in response to external stimuli are therefore desirable to introduce additional operational degree of f...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092410/ https://www.ncbi.nlm.nih.gov/pubmed/30108234 http://dx.doi.org/10.1038/s41598-018-29778-9 |
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author | Zhang, Ziyang Wang, Yaoyuan Wang, Guanghan Mu, Jiaming Ma, Mingyuan He, Yuhan Yang, Rongrong Li, Huanglong |
author_facet | Zhang, Ziyang Wang, Yaoyuan Wang, Guanghan Mu, Jiaming Ma, Mingyuan He, Yuhan Yang, Rongrong Li, Huanglong |
author_sort | Zhang, Ziyang |
collection | PubMed |
description | Electrochemical metallization (ECM) cell kinetics are strongly determined by the electrolyte and can hardly be altered after the cell has been fabricated. Solid-state property tunable electrolytes in response to external stimuli are therefore desirable to introduce additional operational degree of freedom to the ECM cells, enabling novel applications such as multistate memory and reconfigurable computation. In this work, we use Ge(2)Sb(2)Te(5)(GST) as the electrolyte material whose solid state is switched from the amorphous(a) to the crystalline(c) phase thermally. Electrical heating too is readily achievable. The resistive switching characteristics of the cells with different GST phases are examined. The magnitude of the high resistance, the SET voltage and the on/off ratio are found to be considerably affected by the solid phase of GST, whereas the magnitude of the low resistance is least affected. Moreover, a transition from volatile to nonvolatile SET switching is only observed for c-GST based cell under prolonged voltage sweep, but not for a-GST based cell. This work provides a springboard for more studies on the manipulation of the ECM cell kinetics by tunable electrolyte and the resulting unprecedented device functionalities. |
format | Online Article Text |
id | pubmed-6092410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60924102018-08-20 Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte Zhang, Ziyang Wang, Yaoyuan Wang, Guanghan Mu, Jiaming Ma, Mingyuan He, Yuhan Yang, Rongrong Li, Huanglong Sci Rep Article Electrochemical metallization (ECM) cell kinetics are strongly determined by the electrolyte and can hardly be altered after the cell has been fabricated. Solid-state property tunable electrolytes in response to external stimuli are therefore desirable to introduce additional operational degree of freedom to the ECM cells, enabling novel applications such as multistate memory and reconfigurable computation. In this work, we use Ge(2)Sb(2)Te(5)(GST) as the electrolyte material whose solid state is switched from the amorphous(a) to the crystalline(c) phase thermally. Electrical heating too is readily achievable. The resistive switching characteristics of the cells with different GST phases are examined. The magnitude of the high resistance, the SET voltage and the on/off ratio are found to be considerably affected by the solid phase of GST, whereas the magnitude of the low resistance is least affected. Moreover, a transition from volatile to nonvolatile SET switching is only observed for c-GST based cell under prolonged voltage sweep, but not for a-GST based cell. This work provides a springboard for more studies on the manipulation of the ECM cell kinetics by tunable electrolyte and the resulting unprecedented device functionalities. Nature Publishing Group UK 2018-08-14 /pmc/articles/PMC6092410/ /pubmed/30108234 http://dx.doi.org/10.1038/s41598-018-29778-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Ziyang Wang, Yaoyuan Wang, Guanghan Mu, Jiaming Ma, Mingyuan He, Yuhan Yang, Rongrong Li, Huanglong Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte |
title | Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte |
title_full | Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte |
title_fullStr | Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte |
title_full_unstemmed | Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte |
title_short | Electrochemical metallization cell with solid phase tunable Ge(2)Sb(2)Te(5) electrolyte |
title_sort | electrochemical metallization cell with solid phase tunable ge(2)sb(2)te(5) electrolyte |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092410/ https://www.ncbi.nlm.nih.gov/pubmed/30108234 http://dx.doi.org/10.1038/s41598-018-29778-9 |
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