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Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities
The ability for artificially reproducing human brain type signals’ processing is one of the main challenges in modern information technology, being one of the milestones for developing global communicating networks and artificial intelligence. Electronic devices termed memristors have been proposed...
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/PMC6279771/ https://www.ncbi.nlm.nih.gov/pubmed/30514894 http://dx.doi.org/10.1038/s41467-018-07330-7 |
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author | Milano, Gianluca Luebben, Michael Ma, Zheng Dunin-Borkowski, Rafal Boarino, Luca Pirri, Candido F. Waser, Rainer Ricciardi, Carlo Valov, Ilia |
author_facet | Milano, Gianluca Luebben, Michael Ma, Zheng Dunin-Borkowski, Rafal Boarino, Luca Pirri, Candido F. Waser, Rainer Ricciardi, Carlo Valov, Ilia |
author_sort | Milano, Gianluca |
collection | PubMed |
description | The ability for artificially reproducing human brain type signals’ processing is one of the main challenges in modern information technology, being one of the milestones for developing global communicating networks and artificial intelligence. Electronic devices termed memristors have been proposed as effective artificial synapses able to emulate the plasticity of biological counterparts. Here we report for the first time a single crystalline nanowire based model system capable of combining all memristive functions – non-volatile bipolar memory, multilevel switching, selector and synaptic operations imitating Ca(2+) dynamics of biological synapses. Besides underlying common electrochemical fundamentals of biological and artificial redox-based synapses, a detailed analysis of the memristive mechanism revealed the importance of surfaces and interfaces in crystalline materials. Our work demonstrates the realization of self-assembled, self-limited devices feasible for implementation via bottom up approach, as an attractive solution for the ultimate system miniaturization needed for the hardware realization of brain-inspired systems. |
format | Online Article Text |
id | pubmed-6279771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62797712018-12-06 Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities Milano, Gianluca Luebben, Michael Ma, Zheng Dunin-Borkowski, Rafal Boarino, Luca Pirri, Candido F. Waser, Rainer Ricciardi, Carlo Valov, Ilia Nat Commun Article The ability for artificially reproducing human brain type signals’ processing is one of the main challenges in modern information technology, being one of the milestones for developing global communicating networks and artificial intelligence. Electronic devices termed memristors have been proposed as effective artificial synapses able to emulate the plasticity of biological counterparts. Here we report for the first time a single crystalline nanowire based model system capable of combining all memristive functions – non-volatile bipolar memory, multilevel switching, selector and synaptic operations imitating Ca(2+) dynamics of biological synapses. Besides underlying common electrochemical fundamentals of biological and artificial redox-based synapses, a detailed analysis of the memristive mechanism revealed the importance of surfaces and interfaces in crystalline materials. Our work demonstrates the realization of self-assembled, self-limited devices feasible for implementation via bottom up approach, as an attractive solution for the ultimate system miniaturization needed for the hardware realization of brain-inspired systems. Nature Publishing Group UK 2018-12-04 /pmc/articles/PMC6279771/ /pubmed/30514894 http://dx.doi.org/10.1038/s41467-018-07330-7 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 Milano, Gianluca Luebben, Michael Ma, Zheng Dunin-Borkowski, Rafal Boarino, Luca Pirri, Candido F. Waser, Rainer Ricciardi, Carlo Valov, Ilia Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities |
title | Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities |
title_full | Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities |
title_fullStr | Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities |
title_full_unstemmed | Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities |
title_short | Self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities |
title_sort | self-limited single nanowire systems combining all-in-one memristive and neuromorphic functionalities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279771/ https://www.ncbi.nlm.nih.gov/pubmed/30514894 http://dx.doi.org/10.1038/s41467-018-07330-7 |
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