Hybrid magnetic iron oxide nanoparticles with tunable field-directed self-assembly.

We describe the synthesis of hybrid magnetic ellipsoidal nanoparticles that consist of a mixture of two different iron oxide phases, hematite (α-Fe2O3) and maghemite (γ-Fe2O3), and characterize their magnetic field-driven self-assembly. We demonstrate that the relative amount of the two phases can be adjusted in a continuous way by varying the reaction time during the synthesis, leading to strongly varying magnetic properties of the particles. Not only does the saturation magnetization increase dramatically as the composition of the spindles changes from hematite to maghemite, but also the direction of the induced magnetic moment changes from being parallel to the short axis of the spindle to being perpendicular to it. The magnetic dipolar interaction between the particles can be further tuned by adding a screening silica shell. Small-angle X-ray scattering (SAXS) experiments reveal that at high magnetic field, magnetic dipole-dipole interaction forces the silica coated particles to self-assemble into a distorted hexagonal crystal structure at high maghemite content. However, in the case of uncoated maghemite particles, the crystal structure is not very prominent. We interpret this as a consequence of the strong dipolar interaction between uncoated spindles that then become arrested during field-induced self-assembly into a structure riddled with defects.

Tuning the colloidal crystal structure of magnetic particles by external field.

Manipulation of the self-assembly of magnetic colloidal particles by an externally applied magnetic field paves a way toward developing novel stimuli responsive photonic structures. Using microradian X-ray scattering technique we have investigated the different crystal structures exhibited by self-assembly of core-shell magnetite/silica nanoparticles. An external magnetic field was employed to tune the colloidal crystallization. We find that the equilibrium structure in absence of the field is random hexagonal close-packed (RHCP) one. External field drives the self-assembly toward a body-centered tetragonal (BCT) structure. Our findings are in good agreement with simulation results on the assembly of these particles.

Colloidal crystallization and structural changes in suspensions of silica/magnetite core-shell nanoparticles.

The microradian X-ray scattering technique is used to investigate the colloidal crystallization of silica/magnetite core-shell magnetic nanoparticles. Particle self-assembly ranging from 2D sheets to 3D semicrystalline structures is observed as a function of the sedimentation-induced variation of the local particle concentration and the applied magnetic field. Because the particle size is comparable to the wavelength of light, these structures possess photonic properties that can be manipulated by an external stimulus.

Self-assembly and magnetically induced phase transition of three-dimensional colloidal photonic crystals.

Charged superparamagnetic colloidal Fe(3)O(4)@SiO(2) core-shell particles were chosen as model dipolar soft spheres to study their crystallization and magnetically induced phase transition in suspensions. The 3D colloidal crystals feature excellent magnetically responsive photonic properties with strong diffraction, fast response and wide tunability.