Metal Core-Shell Nanoparticle Supercrystals: From Photoactivation of Hydrogen Evolution to Photocorrosion.

Gas nanobubbles are directly linked to many important chemical reactions. While they can be detrimental to operational devices, they also reflect the local activity at the nanoscale. Here, supercrystals made of highly monodisperse Ag@Pt core-shell nanoparticles are first grown onto a solid support and fully characterized by electron microscopies and X-ray scattering.

The five shades of oleylamine in a morphological transition of cobalt nanospheres to nanorods.

Understanding of cobalt nanorods' (Co NRs) formation still remains challenging when it comes to enhancing their anisotropic properties applicable in magnetic or catalytic areas. Herein, we propose a mechanism for the morphological transition from spherical cobalt nanoparticles (NPs) to Co NRs over time (9 h) in a mixture of [CoCl(PPh)] and oleylamine (OAm). In the literature, we described how spherical Co NPs are synthesized via a disproportionation process.

Chemical Evolution of Pt-Zn Nanoalloys Dressed in Oleylamine.

We report on the shape, composition (from PtZn to PtZn), and surface chemistry of Pt-Zn nanoparticles obtained by reduction of precursors M(acac) (M: Pt and Zn) in oleylamine, which serves as both solvent and ligand. We show first that the addition of phenyl ether or benzyl ether determines the composition and shape of the nanoparticles, which point to an adsorbate-controlled synthesis. The organic (ligand)/inorganic (nanoparticles) interface is characterized on the structural and chemical level.

Protective Effect of Polyoxometalates in {Mo}/Maghemite Binary Superlattices Under Annealing.

The binary assembly DDA-{Mo}/OA-γ-FeO (DDA = didodecyldimethylammonium, {Mo} = [MoO(CHCOO)(HO)], OA = oleic acid) constitutes one of the two examples in the literature of binary superlattices made of a mixing of nanocrystals and oxo-clusters. In a precedent work, we reported in details the preparation of such magnetic binary systems and studied the effect of the nature of the polyoxometalates (POMs) on the magnetic properties. In the present paper, we study the stability of this model binary assembly under heating at various temperatures.

Directed Organization of Platinum Nanocrystals through Organic Supramolecular Nanoporous Templates.

We propose a novel approach to trap 2 nm Pt nanocrystals using nanoporous two-dimensional supramolecular networks for cavity-confined host-guest recognition process. This will be achieved by taking advantage of two features of supramolecular self-assembly at surfaces: First, its capability to allow the formation of complex 2D architectures, more particularly, nanoporous networks, through noncovalent interactions between organic molecular building-blocks; second, the ability of the nanopores to selectively host and immobilize a large variety of guest species. In this paper, for the first time, we will use isotropic honeycomb networks and anisotropic linear porous supramolecular networks to host 2 nm Pt nanocrystals.

Binary Superlattices from {Mo132} Polyoxometalates and Maghemite Nanocrystals: Long-Range Ordering and Fine-Tuning of Dipole Interactions.

In the present article, the successful coassembly of spherical 6.2 nm maghemite (γ-Fe2O3) nanocrystals and giant polyoxometalates (POMs) such as 2.9 nm {Mo132} is demonstrated.

Platinum and platinum based nanoalloys synthesized by wet chemistry.

Platinum nanocrystals and their derivatives with palladium and cobalt are of fundamental interest due to their wide field of application in chemistry and physics. Their properties are strongly dependent on their shape and composition. However the chemical route is far from allowing control of both shape and composition.

Role of the nanocrystallinity on the chemical ordering of Co(x)Pt(100-x) nanocrystals synthesized by wet chemistry.

Co(x)Pt(100-x) nanoalloys have been synthesized by two different chemical processes either at high or at low temperature. Their physical properties and the order/disorder phase transition induced by annealing have been investigated depending on the route of synthesis. It is demonstrated that the chemical synthesis at high temperature allows stabilization of the fcc structure of the native nanoalloys while the soft chemical approach yields mainly poly or non crystalline structure.

Synthesis of tin nanocrystals in room temperature ionic liquids.

The aim of this work was to investigate the synthesis of tin nanoparticles (NPs) or tin/carbon composites, in room temperature ionic liquids (RTILs), that could be used as structured anode materials for Li-ion batteries. An innovative route for the synthesis of Sn nanoparticles in such media is successfully developed. Compositions, structures, sizes and morphologies of NPs were characterized by high-energy X-ray diffraction (HEXRD), X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HRTEM).

Influence of hydrogen on the morphology of platinum and palladium nanocrystals.

Palladium and platinum nanocrystals are synthesized by the liquid-liquid phase transfer method, which is a suitable way to produce anisotropic metallic nanoparticles and control their shape at the nanoscopic scale. The process leading to shape control is, however, quite complex as all the physical and chemical parameters could play an important role. In this paper, we have demonstrated the primordial role of the dissolved gases (O(2), H(2), N(2)) in the solvent medium on the nanomorphology of platinum and palladium nanocrystals.