Anisotropic magnetic polymer nanocomposite with self-assembled chains of titania-coated magnetite nanoparticles

An anisotropic magnetic nanocomposite has been prepared by incorporating magnetite nanoparticles (average size: 19nm) in titania (TiO2) particles with a typical size of about 100nm, which are sub- sequently dispersed in a liquid epoxy monomer cured under an inhomogeneous magnetic field. The magnetic force triggers the formation of elongated, self-assembled chains made of aggregated titania particles containing the magnetic cores. The chains have an average length of 7 × 10-5 m and are almost homogeneously distributed throughout the sample; their length and degree of directional order decrease with distance from the magnet producing the magnetic field. FC/ZFC curves and isothermal hysteresis loops of the anisotropic nanocomposite have been studied under a magnetic field applied either parallel or perpendicular to the chains. The anisotropy of the magnetic response is explained by modeling the chains as individual magnetic entities at the mesoscopic level owing to the magnetic dipolar interaction among the embedded magnetite nanoparticles.

Fe3O4 nanoparticles and nanocomposites with potential application in biomedicine and in communication technologies: Nanoparticle aggregation, interaction, and effective magnetic anisotropy

Yves Leterrier, Tommaso Nardi, Marco Sangermano

Magnetite nanoparticles with a size of 5-6 nm with potential impact on biomedicine and information/communication technologies were synthesized by thermal decomposition of Fe(acac)(3) and subsequently coated with a silica shell exploiting a water-in-oil synthetic procedure. The as-produced powders (comprised of either Fe3O4 or Fe3O4@silica nanoparticles) were mixed with a photocurable resin obtaining two magnetic nanocomposites with the same nominal amount of magnetic material. The static magnetic properties of the two nanopowders and the corresponding nanocomposites were measured in the 10 K-300 K temperature range. Magnetic measurements are shown here to be able to give unambiguous information on single-particle properties such as particle size and magnetic anisotropy as well as on nanoparticle aggregation and interparticle interaction. A comparison between the size distribution functions obtained from magnetic measurements and from TEM images shows that figures estimated from properly analyzed magnetic measurements are very close to the actual values. In addition, the present analysis allows us to determine the value of the effective magnetic anisotropy and to estimate the anisotropy contribution from the surface. The Field-cooled/ zero field cooled curves reveal a high degree of particle aggregation in the Fe3O4 nanopowder, which is partially reduced by silica coating and strongly decreased by dissolution in the host polymer. In all considered materials, the nanoparticles are magnetically interacting, the interaction strength being a function of nanoparticle environment and being the lowest in the nanocomposite containing bare, well-separate Fe3O4 particles. All samples behave as interacting superparamagnetic materials instead of ideal superparamagnets and follow the corresponding scaling law. (C) 2014 AIP Publishing LLC.

American Institute of Physics2014

Functionally graded polymer nanocomposites using magnetic fields

Tommaso Nardi

Functionally Graded Materials (FGM) are a class of materials in which the composition and the properties gradually change over the volume. The present PhD project aims to generate a full understanding of a novel synthetic strategy for polymeric FGMs based on the magnetophoretic motion of magnetic nanofillers in a polymer matrix under the application of an external magnetic field gradient. Due to its high rate, costâeffectiveness and lowâtoxicity, UV polymerization was considered as the first curing option for the magnetic nanocomposites. The curability problem deriving from the presence of opaque particles was tackled by studying two different systems based on the same hyperbranched acrylated polymer matrix (HBP): one containing bare Fe3O4 nanoparticles whereas the other loaded with Fe3O4@SiO2 coreâshell nanoparticles. The employment of Fe3O4@SiO2 NPs for the synthesis of magnetic polymeric films showed to be effective towards the inclusion of 10âtimes higher particle volume fractions compared to formulations including bare Fe3O4. By adding Fe3O4@SiO2 nanoparticles to the UVâcurable matrix, the motion of the magnetic responsive filler was induced upon the application of magnetic field gradients generated by permanent magnets. The process was speeded up through the employment of a simple setâup composed of two block magnets in repulsion configuration and through the functionalization of the particle surfaces with an acrylated silane. From the experimental analysis of the photocuring process, the residual stresses arising during the photopolymerization of functionally graded composite coatings based on the UVâcurable HBP matrix and Fe3O4@SiO2 nanoparticles were evaluated with a Finite Element Method approach. These coatings were able to consistently decrease the residual stresses at the coatingâsubstrate interface compared to those encountered either in composites with homogeneous compositions or in the pure polymer, provided that reinforcing fillers were concentrated at the coatingâsubstrate interface. If instead nanoparticles were concentrated at the free surface, graded nanocomposite coatings could reduce by as much as 40% the interfacial stress arising from thermal variations, as demonstrated through numerical simulations. Nanoindentation tests were carried out on the surface of polymer nanocomposites exhibiting either graded or homogeneous distributions of Fe3O4@SiO2 nanoparticles in the UVâcurable matrix. It was experimentally shown how only at relatively small indentation depths, large increases in modulus and hardnesswere obtained for graded composites with respect to their homogeneous counterparts. Through a Material Point Method approach, experimental nanoindentation tests were successfully simulated. Finally, nanocomposite systems based on epoxy matrices were considered. In particular, composites with gradients in permittivity were synthesized through the application of a magnetic field to suspensions of highâpermittivity Fe3O4@TiO2 particles in an epoxy resin. The application of the magnetic force not only induced the movement of the particles, but also caused their alignment in high aspect ratio structures, resulting in rather steep permittivity gradients. Numerical simulations clarified how the asâsynthesized materials, employed as insulators, have the potential to efficiently reduce the electric field stress at the electrodeâinsulator interface and have intrinsic durability advantages over their homogeneous counterparts.

EPFL2015

Magnetism and metal-organic self-assembly of rare-earth atoms on decoupling layers

Sébastien Reynaud

This thesis presents investigations of magnetic and structural properties of two dimensional metal-organic frameworks and of single atoms, both adsorbed on decoupling layers grown on metal surfaces, with focus on rare earth elements.We first report on a series of attempts at realizing self-assembled metal-organic networks on different decoupling layers, probed by scanning tunneling microscopy. The aim is to produce regular structures with high surface filling factors such that the magnetic properties of the rare earth atoms in the metal-organic networks can be investigated by X-ray ensemble measurements. The combinations of three molecular ligands (QDC, BDA, ZnTPyP) on three insulating layers (MgO, NaCl, graphene) with Tb as rare earth are reported. Of the three decoupling layers, only graphene is found to allow the synthesis of metal-organic structures. We successfully synthesized large islands of a rare earth-QDC coordination complex, with a majority of fivefold coordination of the rare earth atoms. The same structure is reproduced with Dy and Er.X-ray absorption spectroscopy, X-ray magnetic circular and linear dichroism measurements are then carried out on the Dy- and Er-QDC/gr/Ir(111) networks. Compared to single atoms on gr/Ir(111), both Dy and Er change their

4f

occupancy from 4

f^n

4f^{n-1}

and change their easy axis of magnetization. Both species are paramagnetic when incorporated into the metal-organic structure. The last part of the thesis is devoted to the study of Dy, Ho, and Gd on NaCl thin films. All three atoms display

4f

occupancy of the gas phase. The top-Cl adsorption site is determined with scanning tunneling microscopy. The magnetic properties are probed with X-ray absorption spectroscopy, X-ray magnetic circular and linear dichroism. Ho and Gd are paramagnetic. Dy has out-of-plane anisotropy with open hysteresis at non zero magnetic field. However, thermally assisted quantum tunneling of the magnetization prevents remanence at zero field.

EPFL2022