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Influence of field amplitude and dipolar interactions on the dynamic response of immobilized magnetic nanoparticles: Perpendicular mutual alignment of an alternating magnetic field and the easy axes. / Ambarov, Alexander V.; Zverev, Vladimir S.; Elfimova, Ekaterina A.
в: Physical Review E, Том 107, № 2, 024601, 02.2023.

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@article{c513480706b347dfa228db5537a21088,
title = "Influence of field amplitude and dipolar interactions on the dynamic response of immobilized magnetic nanoparticles: Perpendicular mutual alignment of an alternating magnetic field and the easy axes",
abstract = "In this paper, the dynamic magnetic properties of an ensemble of interacting immobilized magnetic nanoparticles with aligned easy axes in an applied ac magnetic field directed perpendicular to the easy axes are considered. The system models soft, magnetically sensitive composites synthesized from liquid dispersions of the magnetic nanoparticles in a strong static magnetic field, followed by the carrier liquid's polymerization. After polymerization, the nanoparticles lose translational degrees of freedom; they react to an ac magnetic field via N{\'e}el rotation, when the particle's magnetic moment deviates from the easy axis inside the particle body. Based on a numerical solution of the Fokker-Planck equation for the probability density of the magnetic moment orientation, the dynamic magnetization, frequency-dependent susceptibility, and relaxation times of the particle's magnetic moments are determined. It is shown that the system's magnetic response is formed under the influence of competing interactions, such as dipole-dipole, field-dipole, and dipole-easy-axis interactions. The contribution of each interaction to the magnetic nanoparticle's dynamic response is analyzed. The obtained results provide a theoretical basis for predicting the properties of soft, magnetically sensitive composites, which are increasingly used in high-tech industrial and biomedical technologies.",
author = "Ambarov, {Alexander V.} and Zverev, {Vladimir S.} and Elfimova, {Ekaterina A.}",
note = "The authors gratefully acknowledge research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Mathematical Center Project No. 075-02-2022-877).",
year = "2023",
month = feb,
doi = "10.1103/PhysRevE.107.024601",
language = "English",
volume = "107",
journal = "Physical Review E",
issn = "2470-0045",
publisher = "American Physical Society",
number = "2",

}

RIS

TY - JOUR

T1 - Influence of field amplitude and dipolar interactions on the dynamic response of immobilized magnetic nanoparticles: Perpendicular mutual alignment of an alternating magnetic field and the easy axes

AU - Ambarov, Alexander V.

AU - Zverev, Vladimir S.

AU - Elfimova, Ekaterina A.

N1 - The authors gratefully acknowledge research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Mathematical Center Project No. 075-02-2022-877).

PY - 2023/2

Y1 - 2023/2

N2 - In this paper, the dynamic magnetic properties of an ensemble of interacting immobilized magnetic nanoparticles with aligned easy axes in an applied ac magnetic field directed perpendicular to the easy axes are considered. The system models soft, magnetically sensitive composites synthesized from liquid dispersions of the magnetic nanoparticles in a strong static magnetic field, followed by the carrier liquid's polymerization. After polymerization, the nanoparticles lose translational degrees of freedom; they react to an ac magnetic field via Néel rotation, when the particle's magnetic moment deviates from the easy axis inside the particle body. Based on a numerical solution of the Fokker-Planck equation for the probability density of the magnetic moment orientation, the dynamic magnetization, frequency-dependent susceptibility, and relaxation times of the particle's magnetic moments are determined. It is shown that the system's magnetic response is formed under the influence of competing interactions, such as dipole-dipole, field-dipole, and dipole-easy-axis interactions. The contribution of each interaction to the magnetic nanoparticle's dynamic response is analyzed. The obtained results provide a theoretical basis for predicting the properties of soft, magnetically sensitive composites, which are increasingly used in high-tech industrial and biomedical technologies.

AB - In this paper, the dynamic magnetic properties of an ensemble of interacting immobilized magnetic nanoparticles with aligned easy axes in an applied ac magnetic field directed perpendicular to the easy axes are considered. The system models soft, magnetically sensitive composites synthesized from liquid dispersions of the magnetic nanoparticles in a strong static magnetic field, followed by the carrier liquid's polymerization. After polymerization, the nanoparticles lose translational degrees of freedom; they react to an ac magnetic field via Néel rotation, when the particle's magnetic moment deviates from the easy axis inside the particle body. Based on a numerical solution of the Fokker-Planck equation for the probability density of the magnetic moment orientation, the dynamic magnetization, frequency-dependent susceptibility, and relaxation times of the particle's magnetic moments are determined. It is shown that the system's magnetic response is formed under the influence of competing interactions, such as dipole-dipole, field-dipole, and dipole-easy-axis interactions. The contribution of each interaction to the magnetic nanoparticle's dynamic response is analyzed. The obtained results provide a theoretical basis for predicting the properties of soft, magnetically sensitive composites, which are increasingly used in high-tech industrial and biomedical technologies.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85147698785

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000927774100001

U2 - 10.1103/PhysRevE.107.024601

DO - 10.1103/PhysRevE.107.024601

M3 - Article

VL - 107

JO - Physical Review E

JF - Physical Review E

SN - 2470-0045

IS - 2

M1 - 024601

ER -

ID: 34724606