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Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides
Polar oxide interfaces are an important focus of research due to their novel functionality which is not available in the bulk constituents. So far, research has focused mainly on heterointerfaces derived from the perovskite structure. It is important to extend our understanding of electronic reconst...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303864/ https://www.ncbi.nlm.nih.gov/pubmed/25613569 http://dx.doi.org/10.1038/srep07997 |
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author | Li, Zi-An Fontaíña-Troitiño, N. Kovács, A. Liébana-Viñas, S. Spasova, M. Dunin-Borkowski, R. E. Müller, M. Doennig, D. Pentcheva, R. Farle, M. Salgueiriño, V. |
author_facet | Li, Zi-An Fontaíña-Troitiño, N. Kovács, A. Liébana-Viñas, S. Spasova, M. Dunin-Borkowski, R. E. Müller, M. Doennig, D. Pentcheva, R. Farle, M. Salgueiriño, V. |
author_sort | Li, Zi-An |
collection | PubMed |
description | Polar oxide interfaces are an important focus of research due to their novel functionality which is not available in the bulk constituents. So far, research has focused mainly on heterointerfaces derived from the perovskite structure. It is important to extend our understanding of electronic reconstruction phenomena to a broader class of materials and structure types. Here we report from high-resolution transmission electron microscopy and quantitative magnetometry a robust – above room temperature (Curie temperature T(C) ≫ 300 K) – environmentally stable- ferromagnetically coupled interface layer between the antiferromagnetic rocksalt CoO core and a 2–4 nm thick antiferromagnetic spinel Co(3)O(4) surface layer in octahedron-shaped nanocrystals. Density functional theory calculations with an on-site Coulomb repulsion parameter identify the origin of the experimentally observed ferromagnetic phase as a charge transfer process (partial reduction) of Co(3+) to Co(2+) at the CoO/Co(3)O(4) interface, with Co(2+) being in the low spin state, unlike the high spin state of its counterpart in CoO. This finding may serve as a guideline for designing new functional nanomagnets based on oxidation resistant antiferromagnetic transition metal oxides. |
format | Online Article Text |
id | pubmed-4303864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43038642015-02-03 Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides Li, Zi-An Fontaíña-Troitiño, N. Kovács, A. Liébana-Viñas, S. Spasova, M. Dunin-Borkowski, R. E. Müller, M. Doennig, D. Pentcheva, R. Farle, M. Salgueiriño, V. Sci Rep Article Polar oxide interfaces are an important focus of research due to their novel functionality which is not available in the bulk constituents. So far, research has focused mainly on heterointerfaces derived from the perovskite structure. It is important to extend our understanding of electronic reconstruction phenomena to a broader class of materials and structure types. Here we report from high-resolution transmission electron microscopy and quantitative magnetometry a robust – above room temperature (Curie temperature T(C) ≫ 300 K) – environmentally stable- ferromagnetically coupled interface layer between the antiferromagnetic rocksalt CoO core and a 2–4 nm thick antiferromagnetic spinel Co(3)O(4) surface layer in octahedron-shaped nanocrystals. Density functional theory calculations with an on-site Coulomb repulsion parameter identify the origin of the experimentally observed ferromagnetic phase as a charge transfer process (partial reduction) of Co(3+) to Co(2+) at the CoO/Co(3)O(4) interface, with Co(2+) being in the low spin state, unlike the high spin state of its counterpart in CoO. This finding may serve as a guideline for designing new functional nanomagnets based on oxidation resistant antiferromagnetic transition metal oxides. Nature Publishing Group 2015-01-23 /pmc/articles/PMC4303864/ /pubmed/25613569 http://dx.doi.org/10.1038/srep07997 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Li, Zi-An Fontaíña-Troitiño, N. Kovács, A. Liébana-Viñas, S. Spasova, M. Dunin-Borkowski, R. E. Müller, M. Doennig, D. Pentcheva, R. Farle, M. Salgueiriño, V. Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides |
title | Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides |
title_full | Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides |
title_fullStr | Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides |
title_full_unstemmed | Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides |
title_short | Electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides |
title_sort | electrostatic doping as a source for robust ferromagnetism at the interface between antiferromagnetic cobalt oxides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303864/ https://www.ncbi.nlm.nih.gov/pubmed/25613569 http://dx.doi.org/10.1038/srep07997 |
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