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Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2)
Polar magnetic materials exhibiting appreciable asymmetric exchange interactions can potentially host new topological states of matter such as vortex-like spin textures; however, realizations have been mostly limited to half-integer spins due to rare numbers of integer spin systems with broken spati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658994/ https://www.ncbi.nlm.nih.gov/pubmed/34885793 http://dx.doi.org/10.3390/molecules26237210 |
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author | Oyeka, Ebube E. Winiarski, Michał J. Tran, Thao T. |
author_facet | Oyeka, Ebube E. Winiarski, Michał J. Tran, Thao T. |
author_sort | Oyeka, Ebube E. |
collection | PubMed |
description | Polar magnetic materials exhibiting appreciable asymmetric exchange interactions can potentially host new topological states of matter such as vortex-like spin textures; however, realizations have been mostly limited to half-integer spins due to rare numbers of integer spin systems with broken spatial inversion lattice symmetries. Here, we studied the structure and magnetic properties of the S = 1 integer spin polar magnet β-Ni(IO(3))(2) (Ni(2+), d(8), (3)F). We synthesized single crystals and bulk polycrystalline samples of β-Ni(IO(3))(2) by combining low-temperature chemistry techniques and thermal analysis and characterized its crystal structure and physical properties. Single crystal X-ray and powder X-ray diffraction measurements demonstrated that β-Ni(IO(3))(2) crystallizes in the noncentrosymmetric polar monoclinic structure with space group P2(1). The combination of the macroscopic electric polarization driven by the coalignment of the (IO(3))(−) trigonal pyramids along the b axis and the S = 1 state of the Ni(2+) cation was chosen to investigate integer spin and lattice dynamics in magnetism. The effective magnetic moment of Ni(2+) was extracted from magnetization measurements to be 3.2(1) µ(B), confirming the S = 1 integer spin state of Ni(2+) with some orbital contribution. β-Ni(IO(3))(2) undergoes a magnetic ordering at T = 3 K at a low magnetic field, μ(0)H = 0.1 T; the phase transition, nevertheless, is suppressed at a higher field, μ(0)H = 3 T. An anomaly resembling a phase transition is observed at T ≈ 2.7 K in the C(p)/T vs. T plot, which is the approximate temperature of the magnetic phase transition of the material, indicating that the transition is magnetically driven. This work offers a useful route for exploring integer spin noncentrosymmetric materials, broadening the phase space of polar magnet candidates, which can harbor new topological spin physics. |
format | Online Article Text |
id | pubmed-8658994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86589942021-12-10 Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2) Oyeka, Ebube E. Winiarski, Michał J. Tran, Thao T. Molecules Article Polar magnetic materials exhibiting appreciable asymmetric exchange interactions can potentially host new topological states of matter such as vortex-like spin textures; however, realizations have been mostly limited to half-integer spins due to rare numbers of integer spin systems with broken spatial inversion lattice symmetries. Here, we studied the structure and magnetic properties of the S = 1 integer spin polar magnet β-Ni(IO(3))(2) (Ni(2+), d(8), (3)F). We synthesized single crystals and bulk polycrystalline samples of β-Ni(IO(3))(2) by combining low-temperature chemistry techniques and thermal analysis and characterized its crystal structure and physical properties. Single crystal X-ray and powder X-ray diffraction measurements demonstrated that β-Ni(IO(3))(2) crystallizes in the noncentrosymmetric polar monoclinic structure with space group P2(1). The combination of the macroscopic electric polarization driven by the coalignment of the (IO(3))(−) trigonal pyramids along the b axis and the S = 1 state of the Ni(2+) cation was chosen to investigate integer spin and lattice dynamics in magnetism. The effective magnetic moment of Ni(2+) was extracted from magnetization measurements to be 3.2(1) µ(B), confirming the S = 1 integer spin state of Ni(2+) with some orbital contribution. β-Ni(IO(3))(2) undergoes a magnetic ordering at T = 3 K at a low magnetic field, μ(0)H = 0.1 T; the phase transition, nevertheless, is suppressed at a higher field, μ(0)H = 3 T. An anomaly resembling a phase transition is observed at T ≈ 2.7 K in the C(p)/T vs. T plot, which is the approximate temperature of the magnetic phase transition of the material, indicating that the transition is magnetically driven. This work offers a useful route for exploring integer spin noncentrosymmetric materials, broadening the phase space of polar magnet candidates, which can harbor new topological spin physics. MDPI 2021-11-28 /pmc/articles/PMC8658994/ /pubmed/34885793 http://dx.doi.org/10.3390/molecules26237210 Text en © 2021 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 Oyeka, Ebube E. Winiarski, Michał J. Tran, Thao T. Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2) |
title | Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2) |
title_full | Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2) |
title_fullStr | Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2) |
title_full_unstemmed | Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2) |
title_short | Study of Integer Spin S = 1 in the Polar Magnet β-Ni(IO(3))(2) |
title_sort | study of integer spin s = 1 in the polar magnet β-ni(io(3))(2) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8658994/ https://www.ncbi.nlm.nih.gov/pubmed/34885793 http://dx.doi.org/10.3390/molecules26237210 |
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