We study the influence of surface passivating ligands on the optical and structural properties of zinc blende CdSe nanoplatelets. Ligand exchange of native oleic acid with aliphatic thiol or phosphonic acid on the surface of nanoplatelets results in a large shift of exciton transition energy for up to 240 meV. Ligand exchange also leads to structural changes (strain) in the nanoplatelet's core analysed by wide-angle X-ray diffraction. By correlating the experimental data with theoretical calculations we demonstrate that the exciton energy shift is mainly caused by the ligand-induced anisotropic transformation of the crystalline structure altering the well width of the CdSe core. Further the exciton reduced mass in these CdSe quantum wells is determined by a new method and this agrees well with the expected values substantiating that ligand-strain induced changes in the colloidal quantum well thickness are responsible for the observed spectral shifts. Our findings are important for theoretical modeling of other anisotropically strained systems and demonstrate an approach to tune the optical properties of 2D semiconductor nanocrystals over a broad region thus widening the range of possible applications of AB nanoplatelets in optics and optoelectronics.

Do not tumble dry: Gadolinium-DOTA encapsulated into polysaccharide nanoparticles (GdDOTA NPs) exhibited high relaxivity (r(1) =101.7 s(-1) mM(-1) per Gd(3+) ion at 37 °C and 20 MHz). This high relaxation rate is due to efficient Gd loading, reduced tumbling of the Gd complex, and the hydrogel nature of the nanoparticles. The efficacy of the nanoparticles as a T(1)/T(2) dual-mode contrast agent was studied in C6 cells.

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In this paper we report for the first time on the room temperature template synthesis of germanium and silicon nanowires by potentiostatic electrochemical deposition from the air- and water stable ionic liquid 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)amide ([Py(1,4)]Tf(2)N) containing GeCl(4) and SiCl(4) as a Ge and Si source, respectively. Commercially-available track-etched polycarbonate membranes (PC) with an average nominal pore diameter of 90-400 nm were used as templates. Ge and Si nanowires with an average diameter corresponding to the nanopores' diameter and lengths of a few micrometres were reproducibly obtained. Structural characterization of the nanowires was performed by EDX, TEM, HR-SEM and Raman spectroscopy. Despite the rough surface of the nanowires, governed mostly by the original shape of the nanopore's wall of the commercially-available PC membrane, preliminary structural characterizations demonstrate the promising prospective of this innovative elaboration process compared to constraining high vacuum and high temperature methods.

Silicon nanowires were fabricated for the first time by electrochemical template synthesis at room temperature. This innovative, cheap, and simple process consists of electroreduction of Si ions using a nonaqueous solvent and insulating nanoporous membranes with average pore diameters from 400 to 15 nm which fix the nanowires diameters. Characterization techniques such as scanning and transmission electron microscopies, infrared absorption measurements, X-ray diffraction experiments, energy dispersive X-ray, and Raman spectrometries show that the as-deposited silicon nanowires are amorphous, composed of pure Si and homogeneous in sizes with average diameters and lengths well matching with the nanopores' diameters and the thicknesses of the membranes. Thanks to annealing treatments, it is possible to crystallize the Si nanowires, demonstrating the potentiality for this innovative electrochemical process to obtain a wide range of Si nanowires with well controlled diameters and lengths.

A wide range of amorphous hydrogenated silicon nitride thin films with an excess of silicon was prepared by evaporation of silicon under a flow of nitrogen and hydrogen ions. A strong visible photoluminescence at room temperature was observed for the as-deposited films as well as for films annealed up to 1100°C. The chemical composition and the structure of the films were investigated using x-ray photoelectron, thermal desorption, and Raman spectroscopies, infrared absorption measurements, grazing incidence x-ray diffraction experiments, and transmission electron microscopy. Two luminescence mechanisms were identified for the films depending on the annealing temperature. For annealing temperatures below 650°C, the films are made of amorphous silicon-rich phases mixed with nitrogen-rich phases. These inhomogeneities in the chemical composition, coupled with the evolution of the photoluminescence energies and intensities with the hydrogen content, suggest that the emission is due to the recombination process of the photogenerated carriers within the band-tail states. For temperatures higher than 800°C, a phase separation occurs and the films could be described as silicon nanoclusters embedded in an insulating amorphous silicon nitride matrix. The clusters are amorphous, and then crystallized when the annealing temperature is high enough. The correlation between the clusters sizes and the photoluminescence results suggests that the emission observed after annealing treatments at temperature higher than 900°C is due to the quantum confinement of the carriers inside the silicon clusters. By carefully choosing the preparation and the annealing conditions, it is possible to tune the photoluminescence energy in the visible range.

A series of hydrogel nanoparticles incorporating MRI contrast agents (GdDOTP and MS325) as potential cross-linkers were elaborated by an easy and robust ionotropic gelation process.

For investigating Alzheimer's disease mechanisms, high-speed atomic force microscopy is a proper tool to monitor the interactions between toxic peptides and lipid model membranes.