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Dichotomous dynamics of magnetic monopole fluids

Abstract:
A recent advance in the study of emergent magnetic monopoles was the discovery that monopole motion is restricted to dynamical fractal trajectories [J. N. Hallén et al., Science 378, 1218 (2022)], thus explaining the characteristics of magnetic monopole noise spectra [R. Dusad et al., Nature 571, 234 (2019); A. M. Samarakoon et al., Proc. Natl. Acad. Sci. U.S.A. 119, e2117453119 (2022)]. Here, we apply this novel theory to explore the dynamics of field-driven monopole currents, finding them composed of two quite distinct transport processes: initially swift fractal rearrangements of local monopole configurations followed by conventional monopole diffusion. This theory also predicts a characteristic frequency dependence of the dissipative loss angle for AC field–driven currents. To explore these novel perspectives on monopole transport, we introduce simultaneous monopole current control and measurement techniques using SQUID-based monopole current sensors. For the canonical material Dy2Ti2O7, we measure Φ(t), the time dependence of magnetic flux threading the sample when a net monopole current J(t) = Φ̇ (t)∕0 is generated by applying an external magnetic field B0(t). These experiments find a sharp dichotomy of monopole currents, separated by their distinct relaxation time constants before and after t ~600 μs from monopole current initiation. Application of sinusoidal magnetic fields B0(t) = Bcos(t) generates oscillating monopole currents whose loss angle ( f ) exhibits a characteristic transition at frequency f ≈ 1.8 kHz over the same temperature range. Finally, the magnetic noise power is also dichotomic, diminishing sharply after t ~600 μs. This complex phenomenology represents an unprecedented form of dynamical heterogeneity generated by the interplay of fractionalization and local spin configurational symmetry.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1073/pnas.2320384121

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Oncology
Role:
Author
ORCID:
0000-0002-1161-0774
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Oncology
Role:
Author
ORCID:
0000-0001-8672-0233
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Oncology
Role:
Author
ORCID:
0000-0003-0003-8140


Publisher:
National Academy of Sciences
Journal:
Proceedings of the National Academy of Sciences More from this journal
Volume:
121
Issue:
21
Article number:
e2320384121
Place of publication:
United States
Publication date:
2024-05-14
Acceptance date:
2024-04-17
DOI:
EISSN:
1091-6490
ISSN:
0027-8424
Pmid:
38743620


Language:
English
Keywords:
Pubs id:
1996613
Local pid:
pubs:1996613
Deposit date:
2024-05-22

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