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Neutron specular reflectometry (SR) and off-specular scattering (OSS) are nondestructive techniques which, through deuteration, give a high contrast even among chemically identical species and are therefore highly suitable for investigations of soft-matter thin films. Through a combination of these two techniques, the former yielding a density profile in the direction normal to the sample surface and the latter yielding a depth-resolved in-plane lateral structure, one can obtain quite detailed information on buried morphology on length scales ranging from the order of ångströms to ∼10 µm. This is illustrated via quantitative evaluation of data on SR and OSS collected in time-of-flight (ToF) measurements of a set of films composed of immiscible polymer layers, protonated poly(methyl methacrylate) and deuterated polystyrene, undergoing a decomposition process upon annealing. Joint SR and OSS data analysis was performed by the use of a quick and robust originally developed algorithm including a common absolute-scale normalization of both types of scattering, which are intricately linked, constraining the model to a high degree. This, particularly, makes it possible to distinguish readily between different dewetting scenarios driven either by the nucleation and growth of defects (holes, protrusionsetc.) or by thermal fluctuations in the buried interface between layers. Finally, the 2D OSS maps of particular cases are presented in different spaces and qualitative differences are explained, allowing also the qualitative differentiation of the in-plane structure of long-range order, the correlated roughness and bulk defects by a simple inspection of the scattering maps prior to quantitative fits.

We demonstrate using neutron reflectometry that the internal interfaces in a trilayer system of two identical thick polystyrene layers sandwiching a much thinner (deuterated) poly(methyl methacrylate) layer 15 nm thick (viscosity matched with the polystyrene layers) increase in roughness at the same rate. When the lower polystyrene layer is replaced with a layer of the same polymer of much greater molecular mass, two different growths of the interfaces are observed. From the growth of the interface for this asymmetric case in the solid regime using the theoretical prediction of the spinodal instability including slippage at the interface, a value of the Hamaker constant of the system has been extracted in agreement with the calculated value. For the symmetric case the rise time of the instability is much faster.

We study the influence of nanoparticle doping on the lyotropic liquid crystalline phase of the industrial surfactant Brij®30 (C₁₂E₄) and water, doped with spherical polyoxometalate nanoparticles smaller than the characteristic dimensions of the host lamellar phase. We present viscometry and in situ rheology coupled with small-angle X-ray scattering data that show that, with increasing doping concentration, the nanoparticles act to decrease the shear viscosity of the lamellar phase, and that a shear-induced transition to a multilamellar vesicle "onion" phase is pushed to higher shear rates, and in some cases completely suppressed. X-ray data reveal that the nanoparticles remain encapsulated within the membranes of the vesicles, thus indicating a viable method for the fabrication of nanoparticle incorporating organic vesicles.

International audience; We use optical and scanning force microscopy to explore the possibility of switching the stabilityof a bilayer of poly(methyl methacrylate) (PMMA) on polystyrene by simply changing the filmthickness. We show that for thin PMMA layers on thicker polystyrene films, the PMMA layer isunstable to thickness fluctuations. However, polystyrene layers are unstable when they are substantially thinner than the now stable PMMA film. Dewetting morphologies are catalogued as afunction of the thickness of individual polymer layers by identifying which layer is unstable by whichmechanism, be it spinodal dewetting or heterogeneous thermal nucleation. Our results are in goodagreement with a linear stability analysis of the influence of long-range dispersion forces, but alsoindicate the influence of film preparation and small variations of material properties.

Aqueous suspensions of swelling clay minerals exhibit a rich and complex rheological behaviour. In particular, these repulsive systems display strong shear-thinning at very low volume fractions in both the isotropic and gel states. In this paper, we investigate the evolution with shear of the orientational distribution of aqueous clay suspensions by synchrotron-based rheo-SAXS experiments using a Couette device. Measurements in radial and tangential configurations were carried out for two swelling clay minerals of similar morphology and size, Wyoming montmorillonite and Idaho beidellite. The shear evolution of the small angle x-ray scattering (SAXS) patterns displays significantly different features for these two minerals. The detailed analysis of the angular dependence of the SAXS patterns in both directions provides the average Euler angles of the statistical effective particle in the shear plane. We show that for both samples, the average orientation is fully controlled by the local shear stress around the particle. We then apply an effective approach to take into account multiple hydrodynamic interactions in the system. Using such an approach, it is possible to calculate the evolution of viscosity as a function of shear rate from the knowledge of the average orientation of the particles. The viscosity thus recalculated almost perfectly matches the measured values as long as collective effects are not too important in the system.

We discuss the application of in-situ rheological small angle X-ray scattering experiments to the study of complex fluids under shear, implemented using custom Couette cylinder rheometers mounted on the SWING beamline of the SOLEIL Synchrotron. We discuss several applications of this technique to the study of phase transitions in nanoparticle doped liquid crystals and shear alignment of clay suspensions. The concurrent capture of rheological and scattering data provides vital information that relates macroscopic properties such as viscosity to the microstructure of the fluid.

We have used off-specular neutron reflectometry to study the rupture of a thin, deuterated polystyrene layer confined between a silicon substrate and a thick poly(methyl methacrylate) upper layer. After total rupture of the buried layer, the resulting roughness at the interface that controls the total reflection edge gives rise to Yoneda off-specular scattering. This hypothesis is confirmed by specular reflectivity data that can be fitted to an effective error function subsequent to the rupture of the buried layer. The observed increase in the Yoneda peak intensities, integrated along the path of constant momentum transfer qz, can be directly related to the formation of an interdigitated structure upon rupture of the buried layer. A distorted-wave Born approximation is used to quantitatively simulate the form of the off-specular data in terms of an equivalent error function, with fitting parameters in good agreement with the physical properties of the samples and key experimental results.