Magnetic resonance in nanoparticles: between ferro- and paramagnetism
N. Noginova, F. Chen, T. Weaver, E. P. Giannelis, A. B. Bourlinos, and, V.A. Atsarkin

TL;DR
This study investigates the magnetic resonance properties of gamma-Fe2O3 nanoparticles across a temperature range, revealing insights into their anisotropy, relaxation times, and surface effects through electron magnetic resonance analysis.
Contribution
It provides a detailed analysis of EMR spectra of magnetic nanoparticles, introducing a quantization model and exploring surface anisotropy effects, which are novel in understanding nanoparticle magnetism.
Findings
Spectra become broader and shift to lower fields upon cooling.
A narrow spectral component obeys Arrhenius law with T_A ≈ 850 K.
Uniaxial magnetic anisotropy dominates, with formation of dipolar-coupled chains.
Abstract
Magnetic nanoparticles of gamma-Fe2O3 coated by organic molecules and suspended in liquid and solid matrices, as well as a non-diluted magnetic fluid have been studied by electron magnetic resonance (EMR) at 77-380 K. Slightly asymmetric spectra observed at room temperature become much broader, symmetric, and shift to lower fields upon cooling. An additional narrow spectral component (with the line-width of 30 G) is found in the diluted samples, its magnitude obeying the Arrhenius law with the activation temperature of about 850 K. The longitudinal spin-relaxation time, T1 >> 10 ns, was determined by the specially developed modulation method. Angular dependence of the EMR signal position in field-freezing samples unambiguously points to the domination of the uniaxial magnetic anisotropy. Substantial alignment is achieved in moderate freezing fields of 4-5 kG, suggesting formation of…
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