We use hexagonal mesophases made of oil-swollen surfactant-stabilized tubes arranged on a triangular lattice in water and doped with metallic salts as templates for the radiolytic synthesis of nanostructures. The nanostructures formed in this type of soft matrix are bimetallic palladium-platinum porous nanoballs composed of 3D-connected nanowires, of typical thickness 2.5 nm, forming hexagonal cells. We demonstrate using electron microscopy and small-angle X-ray scattering that the pore size of the nanoballs is directly determined by the diameter of the oil tube of the doped mesophases, which we have varied in a controlled fashion from 10 to 55 nm. Bimetallic nanostructures comprising various proportions of palladium and platinum can be synthesized. Their alloy structure was evidenced by X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy, and high-angular dark field scanning transmission electron microscopy experiments. Our templating approach allows therefore the synthesis of bimetallic nanoballs of tunable porosity and composition.

Very long and thin monocrystalline Pd nanowires were synthesized by decomposition using hydrazine vapour treatment of Pd2(DBA)3 confined in the oil phase of a hexagonal mesophase. The mesophase is composed of toluene-swollen tubes, doped with the Pd precursor, stabilized by a monolayer of surfactant and cosurfactant molecules, and arranged on a triangular lattice in water. Our synthesis is selective and the experiments show that both the confinement and the nature of the surfactant are essential to obtain these Pd nanowires.

We report a demonstration of phase-resolved vibrometry, in which out-of-plane sinusoidal motion is assessed by heterodyne holography. In heterodyne holography, the beam in the reference channel is an optical local oscillator (LO). It is frequency-shifted with respect to the illumination beam to enable frequency conversion within the sensor bandwidth. The proposed scheme introduces a strobe LO, where the reference beam is frequency-shifted and modulated in amplitude, to alleviate the issue of phase retrieval. The strobe LO is both tuned around the first optical modulation side band at the vibration frequency, and modulated in amplitude to freeze selected mechanical vibration states sequentially. The phase map of the vibration can then be derived from the demodulation of successive vibration states.

An analytical and numerical study of the linear Saffman-Taylor instability for a Maxwell viscoelastic fluid is presented. Results obtained in a rectangular Hele-Shaw cell are complemented by experiments in a circular cell corroborating the universality of our main result: The base flow becomes unstable and the propagating disturbances develop into crack-like features. The full hydrodynamics equations in a regime where viscoelasticity dominates show that perturbations to the pressure remain Laplacian. Darcy's law is expressed as an infinite series in the cell thickness. An unique dimensionless parameter Delta-bar, equivalent to a relaxation time, controls the growth rate of the perturbation. Delat-bar depends on the applied gradient of pressure, the surface tension, the cell thickness, and the elastic modulus of the fluid. For small values of Delta-bar, Newtonian behavior dominates whereas for higher values of Delta-bar viscoelastic effects appear. For the critical value Dalta-bar ~= 10 a blowup is predicted and fracture-like patterns are observed.

Designing synthetic microenvironments for cellular investigations is a very active area of research at the crossroads of cell biology and materials science. The present work describes the design and functionalization of a three-dimensional (3D) culture support dedicated to the study of neurite outgrowth from neural cells. It is based on a dense self-assembled collagen matrix stabilized by 100-nm-wide interconnected native fibrils without chemical crosslinking. The matrices were made suitable for cell manipulation and direct observation in confocal microscopy by anchoring them to traditional glass supports with a calibrated thickness of ∼50μm. The matrix composition can be readily adapted to specific neural cell types, notably by incorporating appropriate neurotrophic growth factors. Both PC-12 and SH-SY5Y lines respond to growth factors (nerve growth factor and brain-derived neurotrophic factor, respectively) impregnated and slowly released from the support. Significant neurite outgrowth is reported for a large proportion of cells, up to 66% for PC12 and 49% for SH-SY5Y. It is also shown that both growth factors can be chemically conjugated (EDC/NHS) throughout the matrix and yield similar proportions of cells with longer neurites (61% and 52%, respectively). Finally, neurite outgrowth was observed over several tens of microns within the 3D matrix, with both diffusing and immobilized growth factors.

Diblock copolymers of styrene and gelable acryloxy propyl triethoxysilane (APTES) were successfully prepared through Nitroxide-Mediated Polymerization (NMP). Their micellar behaviour in dioxane-methanol solutions was investigated by Small Angle X-ray Scattering (SAXS) and Neutron Scattering (SANS) measurements. The micelles were found to be spherical whatever the copolymer composition with a PS core size varying from 13.5 nm to 37.8 nm depending on the PS chain length and the swelling ratio. The thickness of the PAPTES corona increased from 6.0 nm to 10.8 nm when increasing the PAPTES polymerization degree from 91 to 336. Two micellar structural regimes were identified, depending on the chain length of the PAPTES soluble block. For PAPTES polymerization degrees higher than 100, the PS core radius in dried state RDC can be consistently described by a scaling relationship RDC α (NPS0.34NPAPTES−0.069) and the aggregation number Nagg obeys the relationship Nagg α (NPS0.021NPAPTES−0.21), consistent with previous studies. For polymerization degrees of the soluble block lower than 100, it was shown that RDC and Nagg do not follow the expected scaling relationships with higher values of Nagg, possibly due to complete chain incorporation in the micelle core. After the cross-linking process, a decrease of the hydrodynamic diameter of 1.6 to 4.7 nm was observed. This is mainly due to the corona shrinkage, the aggregation number and the core radius being directly dependent of the parent non-crosslinked micelles.

The reinforcement of elastomers by inorganic fillers, a concept of very high technological importance, is commonly understood to result from the presence of a mechanical network of partially aggregated filler particles. The non-linear mechanical properties, in particular the decrease of the modulus at high strain (Payne effect), are further interpreted to be a consequence of the breakdown of this filler network. There are, however, many open questions concerning the actual nature of the interparticle connections, where a modified polymer layer forming "glassy bridges" constitutes one possibility. In this work, we address this issue with a suitable silica-filled model elastomer, where we characterize the silica dispersion by SANS in combination with reverse Monte-Carlo modeling, and the mobility modification of the polymer by low-field proton NMR spectroscopy. In our samples, we identify a glassy layer as well as a region of intermediate mobility (possibly modified Rouse modes). Based on the structural information from SANS, we are able to quantify the amount of interparticle connections, and correlate it with the magnitude of the Payne effect taken from shear rheology. This works only if we assume that these connections comprise both, the glassy layer as well as the region of intermediate mobility. The amount of glassy immobilized polymer only does not suffice to explain the mechanical properties.