Miriam Varón

Synthesis of Platinum Cubes, Polypods, Cuboctahedrons, and Raspberries Assisted by Cobalt Nanocrystals

The introduction of metallic traces into the synthesis of platinum nanocrystals (Pt NCs) has been investigated as a surfactant-independent means of controlling shape. Various nanocrystal morphologies have been produced without modification of the reaction conditions, composition, and concentration other than the presence of cobalt traces (<5%). In the presence of metallic cobalt (a strong reducer for Pt cations) cubic Pt NCs are obtained, while cobalt ions or gold NCs have no effect on the synthesis, and as a result, polypods are obtained. Intermediate shapes such as cemented cubes or cuboctahedron NCs are also obtained under similar conditions. Thus, various NC shapes can be obtained with subtle changes, which illustrates the high susceptibility and mutability of the NC shape to modification of the reaction kinetics during the early reduction process. Our studies help progress toward a general mechanism for nanocrystal shape control.

Dipolar Magnetism in Ordered and Disordered Low-Dimensional Nanoparticle Assemblies

Magnetostatic (dipolar) interactions between nanoparticles promise to open new ways to design nanocrystalline magnetic materials and devices if the collective magnetic properties can be controlled at the nanoparticle level. Magnetic dipolar interactions are sufficiently strong to sustain magnetic order at ambient temperature in assemblies of closely-spaced nanoparticles with magnetic moments of ≥ 100 μB. Here we use electron holography with sub-particle resolution to reveal the correlation between particle arrangement and magnetic order in self-assembled 1D and quasi-2D arrangements of 15 nm cobalt nanoparticles. In the initial states, we observe dipolar ferromagnetism, antiferromagnetism and local flux closure, depending on the particle arrangement. Surprisingly, after magnetic saturation, measurements and numerical simulations show that overall ferromagnetic order exists in the present nanoparticle assemblies even when their arrangement is completely disordered. Such direct quantification of the correlation between topological and magnetic order is essential for the technological exploitation of magnetic quasi-2D nanoparticle assemblies.

Dipolar Driven Spontaneous Self Assembly of Superparamagnetic Co Nanoparticles into Micrometric Rice-Grain like Structures

Superparamagnetic single crystal single domain Co nanoparticles of 6 nm in diameter evaporated onto highly pyrolytic oriented graphite spontaneously self-assemble into super structures with an elongated shape. These structures have been studied by optical and scanning electron microscopies, atomic and magnetic force microscopy, electron dispersive X-ray analysis, and SQUID magnetometry. We propose that the weak dipolar interactions between superparamagnetic dipoles of the cobalt nanoparticles are responsible for the formation of these structures when the dipolar magnetic interactions are strong enough to influence the general process of self-assembly dominated by van der Waals forces between neighboring nanoparticles and between nanoparticles and the substrate during evaporation of the solvent.

Pt nanocrystal evolution in the presence of Au(III)-salts at room temperature: spontaneous formation of AuPt heterodimers

Room temperature synthesis of AuPt heterodimers is reported using a simple protocol. The role of oleylamine and Pt NCs in the reduction and nucleation of Au has been investigated. There are two unique aspects in this synthesis. Firstly, the synthesis was conducted at room temperature, which enabled the heterodimer growth to progress at a slower rate and thus allowed monitoring of the Au nucleation process. Secondly, these conditions allowed epitaxial growth with no crystal modification at the Au–Pt interphase. The presence of Pt NC seeds markedly accelerated the reaction, serving both as nucleation platforms and as an initial catalytic reducer of the Au ions in solution. The growth of Au on Pt NCs was monitored at different times by UV-vis, HRTEM and XRD.

Analysis of time-dependent conjugation of gold nanoparticles with an antiparkinsonian molecule by using curve resolution methods

In this work, the time-dependent conjugation process between a thiolated molecule (with anti-parkinsonian properties) and gold nanoparticles has been monitored and studied by the combined use of fast acquisition Ultra Violet-Visible (UV-Vis) spectra and the ability of Multivariate Curve Resolution-Alternating Least Squares (MCR-ALS) technique. From the highly informative kinetic profiles obtained it was possible to extract quantitative and qualitative information of the conjugation process which includes i) time-dependent concentration profiles and pure spectra of species involved on conjugation process, ii) estimation of molecule concentration necessary for the completeness of the conjugation reaction, iii) molecule footprint and iv) free energy of molecule adsorption.

Longitudinal domain wall formation in elongated assemblies of ferromagnetic nanoparticles.

Through evaporation of dense colloids of ferromagnetic ~13 nm ε-Co particles onto carbon substrates, anisotropic magnetic dipolar interactions can support formation of elongated particle structures with aggregate thicknesses of 100–400 nm and lengths of up to some hundred microns. Lorenz microscopy and electron holography reveal collective magnetic ordering in these structures. However, in contrast to continuous ferromagnetic thin films of comparable dimensions, domain walls appear preferentially as longitudinal, i.e., oriented parallel to the long axis of the nanoparticle assemblies. We explain this unusual domain structure as the result of dipolar interactions and shape anisotropy, in the absence of inter-particle exchange coupling.