References of "Bender, Philipp Florian 50031246"
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See detailRelating Magnetic Properties and High Hyperthermia Performance of Iron Oxide Nanoflowers
Bender, Philipp Florian UL; Fock, Jeppe; Frandsen, Cathrine et al

in JOURNAL OF PHYSICAL CHEMISTRY C (2018), 122(5), 3068-3077

We investigated, in depth, the interrelations among structure, magnetic properties, relaxation dynamics and magnetic hyperthermia performance of magnetic nanoflowers. The nanoflowers are about 39 nm in ... [more ▼]

We investigated, in depth, the interrelations among structure, magnetic properties, relaxation dynamics and magnetic hyperthermia performance of magnetic nanoflowers. The nanoflowers are about 39 nm in size, and consist of densely packed iron oxide cores. They display a remanent magnetization, which we explain by the exchange coupling between the cores, but we observe indications for internal spin disorder. By polarized small-angle neutron scattering, we unambiguously confirm that, on average, the nanoflowers are preferentially magnetized along one direction. The extracted discrete relaxation time distribution of the colloidally dispersed particles indicates the presence of three distinct relaxation contributions. We can explain the two slower processes by Brownian and classical Néel relaxation, respectively. The additionally observed very fast relaxation contributions are attributed by us to the relaxation of disordered spins within the nanoflowers. Finally, we show that the intrinsic loss power (ILP, magnetic hyperthermia performance) of the nanoflowers measured in colloidal dispersion at high frequency is comparatively large and independent of the viscosity of the surrounding medium. This concurs with our assumption that the observed relaxation in the high frequency range is primarily a result of internal spin relaxation, and possibly connected to the disordered spins within the individual nanoflowers. [less ▲]

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See detailDipolar-coupled moment correlations in clusters of magnetic nanoparticles
Bender, Philipp Florian UL; Wetterskog, E.; Honecker, Dirk UL et al

in Physical Review. B, Condensed Matter (2018), 98

Here, we resolve the nature of the moment coupling between 10-nm dimercaptosuccinic acid–coated magnetic <br />nanoparticles. The individual iron oxide cores were composed of >95% maghemite and ... [more ▼]

Here, we resolve the nature of the moment coupling between 10-nm dimercaptosuccinic acid–coated magnetic <br />nanoparticles. The individual iron oxide cores were composed of >95% maghemite and agglomerated to <br />clusters. At room temperature the ensemble behaved as a superparamagnet according to Mössbauer and magnetization <br />measurements, however, with clear signs of dipolar interactions. Analysis of temperature-dependent <br />ac susceptibility data in the superparamagnetic regime indicates a tendency for dipolar-coupled anticorrelations <br />of the core moments within the clusters. To resolve the directional correlations between the particle moments <br />we performed polarized small-angle neutron scattering and determined the magnetic spin-flip cross section <br />of the powder in low magnetic field at 300 K. We extract the underlying magnetic correlation function of <br />the magnetization vector field by an indirect Fourier transform of the cross section. The correlation function <br />suggests nonstochastic preferential alignment between neighboring moments despite thermal fluctuations, with <br />anticorrelations clearly dominating for next-nearest moments. These tendencies are confirmed by Monte Carlo <br />simulations of such core clusters. [less ▲]

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