RESUMO
Necklace-like magnetite and maghemite nanorings, composed of magnetic nanoparticles (NPs) with average size about 40 nm, have been prepared via a solvothermal process in a colloidal solution by a self-assembly process. The composition, phase, and morphology of these nanorings have been characterized by X-ray diffraction, X-ray absorption, and transmission electron microscopy. In this paper, we discuss the influence of reaction conditions on the formation of nanorings structure including the amount of PVP in starting materials, reaction time, and temperature. On the basis of experimental observation, we supposed that magnetite NPs may first assemble into chains by magnetic dipole-dipole interactions. These dipolar chains, which are metastable structures relative to necklace-like nanorings, then produced the rings. So, the stability of chains may determine the yield, size, and morphologies of necklace-like nanorings.
RESUMO
The core/shell structure of magnetite/carbon colloidal nanoparticles (CNPs) with average size about 190 nm has been prepared via a one-step solvothermal process using ferrocene as a single reactant. The composition, phase, and morphology of the nanostructure have been characterized by X-ray diffraction, and transmission electron microscopy. Magnetic measurements reveal the superparamagnetic nature of the material with a magnetization saturation of 40.2 emu/g at room temperature. Under the induction of an external magnetic field, strong diffraction in the visible light spectrum can be observed in a suspension of CNPs in ethanol and the diffraction wavelength varies with the strength of the external magnetic field. After being stored for eight months in an ethanol solution, these CNPs can still diffract visible lights when a magnetic field was applied, which is attributed to carbon coating and creating carboxyl groups on the surface of carbon shells introducing both a steric hindrance and electrostatic repulsions between magnetite nanoparticles.