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Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2)
The magnetic interactions of iron-rich manganese-based ThMn(12) type rare earth metal intermetallic compounds are extremely complex. The antiferromagnetic structure sublattice and the ferromagnetic structure sublattice had coexisted and competed with each other. Previous works are focus on studying...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099849/ https://www.ncbi.nlm.nih.gov/pubmed/35564295 http://dx.doi.org/10.3390/nano12091586 |
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author | Gao, Penglin Xia, Yuanhua Gong, Jian Ju, Xin |
author_facet | Gao, Penglin Xia, Yuanhua Gong, Jian Ju, Xin |
author_sort | Gao, Penglin |
collection | PubMed |
description | The magnetic interactions of iron-rich manganese-based ThMn(12) type rare earth metal intermetallic compounds are extremely complex. The antiferromagnetic structure sublattice and the ferromagnetic structure sublattice had coexisted and competed with each other. Previous works are focus on studying magnetic properties of RFe(x)Mn(12−x) (x = 0–9.0, Δx = 0.2). In this work, we obtained a detailed magnetic phase diagram for iron-rich ErFe(x)Mn(12−x) series alloy samples with a fine composition increment (Δx = 0.2), and studied the exchange bias effect and magneto-caloric effect of samples. ErFe(x)Mn(12−x) series (x = 7.0–9.0, Δx = 0.2) alloy samples were synthesized by arc melting, and the pure ThMn(12)-type phase structure was confirmed by X-ray diffraction (XRD). The neutron diffraction test was used to confirm the Mn atom preferentially occupying the 8i position and to quantify the Mn. The magnetic properties of the materials were characterized by a comprehensive physical property measurement system (PPMS). Accurate magnetic phase diagrams of the samples in the composition range 7.0–9.0 were obtained. Along with temperature decrease, the samples experienced paramagnetic, ferromagnetic changes for samples with x < 7.4 and x > 8.4, and paramagnetic, antiferromagnetic and ferromagnetic or paramagnetic, ferromagnetic and antiferromagnetic changes for samples with 7.4 ≤ x ≤ 8.2. The tunable exchange bias effect was observed for sample with 7.4 ≤ x ≤ 8.2, which resulting from competing magnetic interacting among ferromagnetic and antiferromagnetic sublattices. The maximum magnetic entropy change in an ErFe(9.0)Mn(3.0) specimen reached 1.92 J/kg/K around room temperature when the magnetic field change was 5 T. This study increases our understanding of exchange bias effects and allows us to better control them. |
format | Online Article Text |
id | pubmed-9099849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90998492022-05-14 Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2) Gao, Penglin Xia, Yuanhua Gong, Jian Ju, Xin Nanomaterials (Basel) Article The magnetic interactions of iron-rich manganese-based ThMn(12) type rare earth metal intermetallic compounds are extremely complex. The antiferromagnetic structure sublattice and the ferromagnetic structure sublattice had coexisted and competed with each other. Previous works are focus on studying magnetic properties of RFe(x)Mn(12−x) (x = 0–9.0, Δx = 0.2). In this work, we obtained a detailed magnetic phase diagram for iron-rich ErFe(x)Mn(12−x) series alloy samples with a fine composition increment (Δx = 0.2), and studied the exchange bias effect and magneto-caloric effect of samples. ErFe(x)Mn(12−x) series (x = 7.0–9.0, Δx = 0.2) alloy samples were synthesized by arc melting, and the pure ThMn(12)-type phase structure was confirmed by X-ray diffraction (XRD). The neutron diffraction test was used to confirm the Mn atom preferentially occupying the 8i position and to quantify the Mn. The magnetic properties of the materials were characterized by a comprehensive physical property measurement system (PPMS). Accurate magnetic phase diagrams of the samples in the composition range 7.0–9.0 were obtained. Along with temperature decrease, the samples experienced paramagnetic, ferromagnetic changes for samples with x < 7.4 and x > 8.4, and paramagnetic, antiferromagnetic and ferromagnetic or paramagnetic, ferromagnetic and antiferromagnetic changes for samples with 7.4 ≤ x ≤ 8.2. The tunable exchange bias effect was observed for sample with 7.4 ≤ x ≤ 8.2, which resulting from competing magnetic interacting among ferromagnetic and antiferromagnetic sublattices. The maximum magnetic entropy change in an ErFe(9.0)Mn(3.0) specimen reached 1.92 J/kg/K around room temperature when the magnetic field change was 5 T. This study increases our understanding of exchange bias effects and allows us to better control them. MDPI 2022-05-07 /pmc/articles/PMC9099849/ /pubmed/35564295 http://dx.doi.org/10.3390/nano12091586 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gao, Penglin Xia, Yuanhua Gong, Jian Ju, Xin Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2) |
title | Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2) |
title_full | Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2) |
title_fullStr | Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2) |
title_full_unstemmed | Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2) |
title_short | Structure and Magnetic Properties of ErFe(x)Mn(12−x) (7.0 ≤ x ≤ 9.0, Δx = 0.2) |
title_sort | structure and magnetic properties of erfe(x)mn(12−x) (7.0 ≤ x ≤ 9.0, δx = 0.2) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099849/ https://www.ncbi.nlm.nih.gov/pubmed/35564295 http://dx.doi.org/10.3390/nano12091586 |
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