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Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics
Understanding the feasibility to couple semiconducting and magnetic properties in metal halide perovskites through interface design opens new opportunities for creating the next generation spin‐related optoelectronics. In this work, a fundamentally new phenomenon of optically induced magnetization a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188215/ https://www.ncbi.nlm.nih.gov/pubmed/34141521 http://dx.doi.org/10.1002/advs.202004488 |
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author | Wang, Miaosheng Xu, Hengxing Wu, Ting Ambaye, Haile Qin, Jiajun Keum, Jong Ivanov, Ilia N. Lauter, Valeria Hu, Bin |
author_facet | Wang, Miaosheng Xu, Hengxing Wu, Ting Ambaye, Haile Qin, Jiajun Keum, Jong Ivanov, Ilia N. Lauter, Valeria Hu, Bin |
author_sort | Wang, Miaosheng |
collection | PubMed |
description | Understanding the feasibility to couple semiconducting and magnetic properties in metal halide perovskites through interface design opens new opportunities for creating the next generation spin‐related optoelectronics. In this work, a fundamentally new phenomenon of optically induced magnetization achieved by coupling photoexcited orbital magnetic dipoles with magnetic spins at perovskite/ferromagnetic interface is discovered. The depth‐sensitive polarized neutron reflectometry combined with in situ photoexcitation setup, constitutes key evidence of this novel effect. It is demonstrated that a circularly polarized photoexcitation induces a stable magnetization signal within the depth up to 7.5 nm into the surface of high‐quality perovskite (MAPbBr(3)) film underneath a ferromagnetic cobalt layer at room temperature. In contrast, a linearly polarized light does not induce any detectable magnetization in the MAPbBr(3). The observation reveals that photoexcited orbital magnetic dipoles at the surface of perovskite are coupled with the spins of the ferromagnetic atoms at the interface, leading to an optically induced magnetization within the perovskite’s surface. The finding demonstrates that perovskite semiconductor can be bridged with magnetism through optically controllable method at room temperature in this heterojunction design. This provides the new concept of utilizing spin and orbital degrees of freedom in new‐generation spin‐related optoelectronic devices. |
format | Online Article Text |
id | pubmed-8188215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81882152021-06-16 Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics Wang, Miaosheng Xu, Hengxing Wu, Ting Ambaye, Haile Qin, Jiajun Keum, Jong Ivanov, Ilia N. Lauter, Valeria Hu, Bin Adv Sci (Weinh) Research Articles Understanding the feasibility to couple semiconducting and magnetic properties in metal halide perovskites through interface design opens new opportunities for creating the next generation spin‐related optoelectronics. In this work, a fundamentally new phenomenon of optically induced magnetization achieved by coupling photoexcited orbital magnetic dipoles with magnetic spins at perovskite/ferromagnetic interface is discovered. The depth‐sensitive polarized neutron reflectometry combined with in situ photoexcitation setup, constitutes key evidence of this novel effect. It is demonstrated that a circularly polarized photoexcitation induces a stable magnetization signal within the depth up to 7.5 nm into the surface of high‐quality perovskite (MAPbBr(3)) film underneath a ferromagnetic cobalt layer at room temperature. In contrast, a linearly polarized light does not induce any detectable magnetization in the MAPbBr(3). The observation reveals that photoexcited orbital magnetic dipoles at the surface of perovskite are coupled with the spins of the ferromagnetic atoms at the interface, leading to an optically induced magnetization within the perovskite’s surface. The finding demonstrates that perovskite semiconductor can be bridged with magnetism through optically controllable method at room temperature in this heterojunction design. This provides the new concept of utilizing spin and orbital degrees of freedom in new‐generation spin‐related optoelectronic devices. John Wiley and Sons Inc. 2021-05-02 /pmc/articles/PMC8188215/ /pubmed/34141521 http://dx.doi.org/10.1002/advs.202004488 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wang, Miaosheng Xu, Hengxing Wu, Ting Ambaye, Haile Qin, Jiajun Keum, Jong Ivanov, Ilia N. Lauter, Valeria Hu, Bin Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics |
title | Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics |
title_full | Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics |
title_fullStr | Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics |
title_full_unstemmed | Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics |
title_short | Optically Induced Static Magnetization in Metal Halide Perovskite for Spin‐Related Optoelectronics |
title_sort | optically induced static magnetization in metal halide perovskite for spin‐related optoelectronics |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188215/ https://www.ncbi.nlm.nih.gov/pubmed/34141521 http://dx.doi.org/10.1002/advs.202004488 |
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