Formation of Superlattices of Gold Nanoparticles Using Ostwald Ripening in Emulsions: Transition from fcc to bcc Structure.

An efficient method to form 3D superlattices of gold nanoparticles inside oil emulsion droplets is presented. We demonstrate that this method relies on Ostwald ripening, a well-known phenomenon occurring during the aging of emulsions. The key point is that the nanoparticle concentration inside the smaller droplets is increasing very slowly with time, thus inducing the crystallization of the nanoparticles into superlattices. Using oil-in-water emulsions doped with hydrophobic gold nanoparticles, we demonstrate that this method is efficient for different types of oils (toluene, cyclohexane, dodecane, and hexadecane). 3D superlattices of the nanoparticles are obtained, with dimensions reaching a hundred nanometers. The kinetics of the crystallization depends on the solubility of the oil in water but also on the initial concentration of the gold nanoparticles in oil. This method also provides an innovative way to obtain the complete phase diagram of nanoparticle suspensions with concentration. Indeed, during this slow crystallization process, a transition from a disordered suspension to a fcc structure is observed, followed by a transition toward a bcc structure. This evolution with time provides key results to understand the role played by the ligands located at the surface of the nanoparticles in order to control the type of superlattices which are formed.

Evidence for a C14 Frank-Kasper Phase in One-Size Gold Nanoparticle Superlattices.

The Frank-Kasper phases were already known in 1982 when quasi-crystals were discovered, but their complex architectures are now considered as making a link between simple close-packed periodic structures and some quasi-periodic ones. These tetrahedrally close packed structures are observed in many materials from elements to intermetallics as well as self-assembled soft materials like micellar systems, dendritric liquid crystals, star polymers, and more recently block copolymers or heated gold nanocrystal superlattices. We report here the existence of a Frank-Kasper phase with hexagonal symmetry (MgZn2 type, also labeled C14) in superlattices of monodisperse hydrophobically coated gold particles at room temperature obtained from suspensions in various solvents. The existence of such a structure in this system is analyzed in terms of geometrical parameters including gold core diameter, ligand length, and grafting density and an energetic approach based on van der Waals attraction. Hydrophobically coated gold nanoparticles is a new system that exhibits a Frank and Kasper phase built by one-size objects. This result opens a route toward a nanoparticle superlattice with complex structures and thus original physical properties.

Solvent-driven interactions between hydrophobically-coated nanoparticles.

Interaction between hydrophobically-coated gold nanoparticles suspended in oil is usually described as the combination of strong attractive van der Waals attraction between the gold cores and interaction between the ligands. The latter interaction is expected to be purely repulsive if the suspending medium is a good solvent for the ligands or partially attractive for a bad solvent. By measuring the structure factor of interacting gold nanoparticles in various solvents, we show that the chemical affinity of the ligand with the solvent is not the only parameter that controls the interaction between the ligands and that the solvent conformation (small rigid or long flexible molecules) also plays a crucial role. Gold nanoparticles covered with hexanethiol or dodecanethiol thus undergo a larger attraction in n-dodecane or n-hexadecane compared to toluene or cyclohexane. As a consequence, self-assembly of these nanoparticles into superlattices appears at a much lower volume fraction than predicted in n-hexadecane or n-dodecane. Analogy with the behavior of polymer grafted colloids in a polymer melt is proposed to explain these unexpected results.