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Electrochemical metallization cell with anion supplying active electrode
Electrochemical metallization (ECM) memories are among the various emerging non-volatile memory technologies, contending to replace DRAM and Flash and enabling novel neuromorphic computing applications. Typically, the operation of ECM cell is based on the electrochemical redox reactions of the catio...
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/PMC6105648/ https://www.ncbi.nlm.nih.gov/pubmed/30135453 http://dx.doi.org/10.1038/s41598-018-30746-6 |
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author | Zhang, Ziyang Wang, Yaoyuan Luo, Yan He, Yuhan Ma, Mingyuan Yang, Rongrong Li, Huanglong |
author_facet | Zhang, Ziyang Wang, Yaoyuan Luo, Yan He, Yuhan Ma, Mingyuan Yang, Rongrong Li, Huanglong |
author_sort | Zhang, Ziyang |
collection | PubMed |
description | Electrochemical metallization (ECM) memories are among the various emerging non-volatile memory technologies, contending to replace DRAM and Flash and enabling novel neuromorphic computing applications. Typically, the operation of ECM cell is based on the electrochemical redox reactions of the cation supplying active electrode (e.g., Ag, Cu). Although extensively investigated, the possibility of utilizing new materials for the active electrode remains largely undiscussed. In this paper, an ECM cell with a Te active electrode is fabricated. It is found that the SET operation of the device occurs under negative voltage on the active electrode, which is opposite to that of the device with Ag electrode, indicating that the Te electrode supplies Te(2−) anions by electrochemical reduction. The influence of the electrolyte material on the switching properties is also found to be more significant for devices with Te electrodes. For Pt/GeS/Te and Pt/Ge(2)Sb(2)Te(5)/Te cells, repeatable unipolar and bipolar resistive switching are observed, respectively, which can be attributed to the rupture of the filament by Joule heating for the former and by ECM for the latter in the RESET process. The semiconducting properties of Te, the reversed operating polarity and the electrolyte dependent switching characteristics open up unprecedented prospects for ECM cells. |
format | Online Article Text |
id | pubmed-6105648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61056482018-08-27 Electrochemical metallization cell with anion supplying active electrode Zhang, Ziyang Wang, Yaoyuan Luo, Yan He, Yuhan Ma, Mingyuan Yang, Rongrong Li, Huanglong Sci Rep Article Electrochemical metallization (ECM) memories are among the various emerging non-volatile memory technologies, contending to replace DRAM and Flash and enabling novel neuromorphic computing applications. Typically, the operation of ECM cell is based on the electrochemical redox reactions of the cation supplying active electrode (e.g., Ag, Cu). Although extensively investigated, the possibility of utilizing new materials for the active electrode remains largely undiscussed. In this paper, an ECM cell with a Te active electrode is fabricated. It is found that the SET operation of the device occurs under negative voltage on the active electrode, which is opposite to that of the device with Ag electrode, indicating that the Te electrode supplies Te(2−) anions by electrochemical reduction. The influence of the electrolyte material on the switching properties is also found to be more significant for devices with Te electrodes. For Pt/GeS/Te and Pt/Ge(2)Sb(2)Te(5)/Te cells, repeatable unipolar and bipolar resistive switching are observed, respectively, which can be attributed to the rupture of the filament by Joule heating for the former and by ECM for the latter in the RESET process. The semiconducting properties of Te, the reversed operating polarity and the electrolyte dependent switching characteristics open up unprecedented prospects for ECM cells. Nature Publishing Group UK 2018-08-22 /pmc/articles/PMC6105648/ /pubmed/30135453 http://dx.doi.org/10.1038/s41598-018-30746-6 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 Luo, Yan He, Yuhan Ma, Mingyuan Yang, Rongrong Li, Huanglong Electrochemical metallization cell with anion supplying active electrode |
title | Electrochemical metallization cell with anion supplying active electrode |
title_full | Electrochemical metallization cell with anion supplying active electrode |
title_fullStr | Electrochemical metallization cell with anion supplying active electrode |
title_full_unstemmed | Electrochemical metallization cell with anion supplying active electrode |
title_short | Electrochemical metallization cell with anion supplying active electrode |
title_sort | electrochemical metallization cell with anion supplying active electrode |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105648/ https://www.ncbi.nlm.nih.gov/pubmed/30135453 http://dx.doi.org/10.1038/s41598-018-30746-6 |
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