No Arabic abstract
Magnetic measurements have been performed on 40-nm sphere-like Fe3O4 nanoparticles using a Quantum Design vibrating sample magnetometer. Coating Fe3O4 nanoparticles with SiO2 effectively eliminates magnetic interparticle interactions so that the coercive field HC in the hightemperature range between 300 K and the Curie temperature (855 K) can be well fitted by an expression for noninteracting randomly oriented single-domain particles. From the fitting parameters, the effective anisotropy constant K is found to be (1.68 pm 0.17) times 105 erg/cm3, which is slightly larger than the bulk magnetocrystalline anisotropy constant of 1.35 times 105 erg/cm3. Moreover, the inferred mean particle diameter from the fitting parameters is in quantitative agreement with that determined from transmission electron microscope. Such a quantitative agreement between data and theory suggests that the assemble of our SiO2-coated sphere-like Fe3O4 nanopartles represents a good system of noninteracting randomly-oriented single-domain particles.
Magnetic nanoparticles (NP) of magnetite (Fe3O4) coated with oleic acid (OA) and dodecanoic acid (DA) were synthesized and investigated through Transmission Electron Microscopy (TEM),magnetization M, and ac magnetic susceptibility measurements. The OA coated samples were produced with different magnetic concentrations (78, 76, and 65%) and the DA sample with 63% of Fe3O4. Images from TEM indicate that the NP have a nearly spherical geometry and mean diameter ~ 5.5 nm. Magnetization measurements, performed in zero field cooled (ZFC) and field cooled (FC) processes under different external magnetic fields H, exhibited a maximum at a given temperature TB in the ZFC curves, which depends on the NP coating (OA or DA), magnetite concentration, and H. The temperature TB decreases monotonically with increasing H and, for a given H, the increase in the magnetite concentration results in an increase of TB. The observed behavior is related to the dipolar interaction (DI) between NP which seems to be an important mechanism in all samples studied. This is supported by the results of the ac magnetic susceptibility Xac measurements, where the temperature in which X peaks for different frequencies follows the Vogel-Fulcher model, a feature commonly found in systems with dipolar interactions. Curves of H vs. TB/TB(H=0) for samples with different coatings and magnetite concentrations collapse into a universal curve, indicating that the qualitative magnetic behavior of the samples may be described by the NP themselves, instead of the coating or the strength of the dipolar interaction. Below TB, M vs. H curves show a coercive field (HC) that increases monotonically with decreasing temperature. The saturation magnetization (MS) follows the Blochs law and values of MS at room temperature as high as 78 emu/g were estimated, a result corresponding to ~80% of the bulk value. The overlap of M/MS vs. H/T curves for a given sample and the low HC at high temperatures suggest superparamagnetic behavior in all samples studied. The overlap of M/MS vs. H curves at constant temperature for different samples indicates that the NP magnetization behavior is preserved, independently of the coating and magnetite concentration.
The numerous phenomenological equations used in the study of the behaviour of single-domain magnetic nanoparticles are described and some issues clarified by means of qualitative comparison. To enable a quantitative textit{application} of the model based on the Debye (exponential) relaxation and the torque driving the Larmor precession, we present analytical solutions for the steady states in presence of circularly and linearly polarized AC magnetic fields. Using the exact analytical solutions, we can confirm the insight that underlies Rosensweigs introduction of the chord susceptibility for an approximate calculation of the losses. As an important consequence, it can also explain experiments, where power dissipation for both fields were found to be identical in root mean square sense. We also find that this approximation provides satisfactory numerical accuracy only up to magnetic fields for which the argument of the Langevin function reaches the value 2.8.
We present a systematic study of core-shell Au/Fe_3O_4 nanoparticles produced by thermal decomposition under mild conditions. The morphology and crystal structure of the nanoparticles revealed the presence of Au core of <d> = (6.9pm 1.0) nm surrounded by Fe_3O_4 shell with a thickness of ~3.5 nm, epitaxially grown onto the Au core surface. The Au/Fe_3O_4 core-shell structure was demonstrated by high angle annular dark field scanning transmission electron microscopy analysis. The magnetite shell grown on top of the Au nanoparticle displayed a thermal blocking state at temperatures below T_B = 59 K and a relaxed state well above T_B. Remarkably, an exchange bias effect was observed when cooling down the samples below room temperature under an external magnetic field. Moreover, the exchange bias field (H_{EX}) started to appear at T~40 K and its value increased by decreasing the temperature. This effect has been assigned to the interaction of spins located in the magnetically disordered regions (in the inner and outer surface of the Fe_3O_4 shell) and spins located in the ordered region of the Fe_3O_4 shell.
The magnetic properties of a monolayer of Mn12 single molecule magnets grafted onto a Si substrate have been investigated using depth-controlled $beta$-detected nuclear magnetic resonance. A low energy beam of spin polarized radioactive 8Li was used to probe the local static magnetic field distribution near the Mn12 monolayer in the Si substrate. The resonance linewidth varies strongly as a function of implantation depth as a result of the magnetic dipolar fields generated by the Mn12 electronic magnetic moments. The temperature dependence of the linewidth indicates that the magnetic properties of the Mn12 moments in this low dimensional configuration differ from bulk Mn12.
Homogeneous single phase GdCrO3 nanoparticles are synthesized by a modified-hydrothermal synthesis. The sample shows a compensation temperature at 128 K, below which the DC magnetization becomes negative and positive at low temperatures due to the competition between the two sublattice magnetization. At Neel temperature (168K), the line width and the intensity show an abrupt transition, revealed from electron paramagnetic resonance spectroscopy.