Quantitative analysis of the specific absorption rate dependence on the magnetic field strength in znxfe3−xo4 nanoparticles

32Citations
Citations of this article
52Readers
Mendeley users who have this article in their library.

Abstract

Superparamagnetic ZnxFe3−xO4 magnetic nanoparticles (0 ≤ x < 0.5) with spherical shapes of 16 nm average diameter and different zinc doping level have been successfully synthesized by co-precipitation method. The homogeneous zinc substitution of iron cations into the magnetite crystalline structure has led to an increase in the saturation magnetization of nanoparticles up to 120 Am2/kg for x ~ 0.3. The specific absorption rate (SAR) values increased considerably when x is varied between 0 and 0.3 and then decreased for x ~ 0.5. The SAR values are reduced upon the immobilization of the nanoparticles in a solid matrix being significantly increased by a pre-alignment step in a uniform static magnetic field before immobilization. The SAR values displayed a quadratic dependence on the alternating magnetic field amplitude (H) up to 35 kA/m. Above this value, a clear saturation effect of SAR was observed that was successfully described qualitatively and quantitatively by considering the non-linear field’s effects and the magnetic field dependence of both Brown and Neel relaxation times. The Neel relaxation time depends more steeply on H as compared with the Brown relaxation time, and the magnetization relaxation might be dominated by the Neel mechanism, even for nanoparticles with large diameter.

Cite

CITATION STYLE

APA

Kerroum, M. A. A., Iacovita, C., Baaziz, W., Ihiawakrim, D., Rogez, G., Benaissa, M., … Ersen, O. (2020). Quantitative analysis of the specific absorption rate dependence on the magnetic field strength in znxfe3−xo4 nanoparticles. International Journal of Molecular Sciences, 21(20), 1–24. https://doi.org/10.3390/ijms21207775

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free