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Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin
Continuous miniaturization of magnetic units in spintronics devices inspires efforts to search for novel 2D magnetic materials with giant magnetic anisotropy energy (MAE). Through systematic first‐principles calculations, large MAE of 24 meV in W or Re embedded 2D polyporphyrin frameworks is found....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644233/ https://www.ncbi.nlm.nih.gov/pubmed/29051849 http://dx.doi.org/10.1002/advs.201700019 |
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author | Wang, Peng Jiang, Xue Hu, Jun Zhao, Jijun |
author_facet | Wang, Peng Jiang, Xue Hu, Jun Zhao, Jijun |
author_sort | Wang, Peng |
collection | PubMed |
description | Continuous miniaturization of magnetic units in spintronics devices inspires efforts to search for novel 2D magnetic materials with giant magnetic anisotropy energy (MAE). Through systematic first‐principles calculations, large MAE of 24 meV in W or Re embedded 2D polyporphyrin frameworks is found. Interestingly, the MAE can be enhanced up to 60 meV, through replacing the hydrogen atoms on the edges of the Re based 2D polyporphyrin framework by hydroxyl and amino radicals. Analysis of the electronic structures reveals that the enhancement of MAE is mainly attributed to charge redistributions and energy shifts of Re 5d orbitals induced by the functional radicals. The findings pave a new and feasible way for tailoring the magnetic properties of magnetic organic materials to fulfill the criteria for applications in spintronics devices at high temperature. |
format | Online Article Text |
id | pubmed-5644233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56442332017-10-19 Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin Wang, Peng Jiang, Xue Hu, Jun Zhao, Jijun Adv Sci (Weinh) Full Papers Continuous miniaturization of magnetic units in spintronics devices inspires efforts to search for novel 2D magnetic materials with giant magnetic anisotropy energy (MAE). Through systematic first‐principles calculations, large MAE of 24 meV in W or Re embedded 2D polyporphyrin frameworks is found. Interestingly, the MAE can be enhanced up to 60 meV, through replacing the hydrogen atoms on the edges of the Re based 2D polyporphyrin framework by hydroxyl and amino radicals. Analysis of the electronic structures reveals that the enhancement of MAE is mainly attributed to charge redistributions and energy shifts of Re 5d orbitals induced by the functional radicals. The findings pave a new and feasible way for tailoring the magnetic properties of magnetic organic materials to fulfill the criteria for applications in spintronics devices at high temperature. John Wiley and Sons Inc. 2017-07-18 /pmc/articles/PMC5644233/ /pubmed/29051849 http://dx.doi.org/10.1002/advs.201700019 Text en © 2017 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Wang, Peng Jiang, Xue Hu, Jun Zhao, Jijun Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin |
title | Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin |
title_full | Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin |
title_fullStr | Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin |
title_full_unstemmed | Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin |
title_short | Chemically Engineering Magnetic Anisotropy of 2D Metalloporphyrin |
title_sort | chemically engineering magnetic anisotropy of 2d metalloporphyrin |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644233/ https://www.ncbi.nlm.nih.gov/pubmed/29051849 http://dx.doi.org/10.1002/advs.201700019 |
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