Unique orientation of 1D and 2D nanoparticle assemblies confined in smectic topological defects.

New collective optical properties have emerged recently from organized and oriented arrays of closely packed semiconducting and metallic nanoparticles (NPs). However, it is still challenging to obtain NP assemblies which are similar everywhere on a given sample and, most importantly, share a unique common orientation that would guarantee a unique behavior everywhere on the sample. In this context, by combining optical microscopy, fluorescence microscopy and synchrotron-based grazing incidence X-ray scattering (GISAXS) of assemblies of gold nanospheres and of fluorescent nanorods, we study the interactions between NPs and liquid crystal smectic topological defects that can ultimately lead to unique NP orientations.

From Chains to Monolayers: Nanoparticle Assembly Driven by Smectic Topological Defects.

In this Letter, we show how advanced hierarchical structures of topological defects in the so-called smectic oily streaks can be used to sequentially transfer their geometrical features to gold nanospheres. We use two kinds of topological defects, 1D dislocations and 2D ribbon-like topological defects. The large trapping efficiency of the smectic dislocation cores not only surpasses that of the elastically distorted zones around the cores but also surpasses the one of the 2D ribbon-like topological defect.

Critical Au Concentration for the Stabilization of Au-Cu Nanoparticles on Rutile against Dissociation under Oxygen.

Controlling aging of catalysts is of crucial importance to preserve their properties, in particular for bimetallic nanoparticles (NPs) where reaction can modify the composition. Herein, we have studied the stability upon oxygen exposure of gold-copper NPs supported on rutile. We have used in situ scanning tunneling microscopy to follow the evolution of individual Au, Cu and Au-Cu NPs with various compositions grown on the TiO2(110) surface, during each step from their nucleation to their modification with oxygen.

Emergence of chirality in hexagonally packed monolayers of hexapentyloxytriphenylene on Au(111): a joint experimental and theoretical study.

We investigate the expression of chirality in a monolayer formed spontaneously by 2,3,6,7,10,11-pentyloxytriphenylene (H5T) on Au(111). We resolve its interface morphology by combining scanning tunneling microscopy (STM) with theoretical calculations of intermolecular and interfacial interaction potentials. We observe two commensurate structures.

Revisiting elastic interactions between steps on vicinal surfaces: the buried dipole model.

We expose a new analytical method for computing elastic displacements and interactions due to steps on vicinal surfaces. The model of a "buried dipole" allows us to take into account the specific geometry of the step while performing anisotropic linear elasticity calculations. The displacements found show a remarkable agreement with molecular dynamics simulations for Cu and Pt (001) and (111) vicinals.

Measuring surface stress discontinuities in self-organized systems with X rays.

We have performed a grazing incidence x-ray diffraction study of the self-organized N/Cu(001) system. Diffraction satellites associated with self-organization are particularly intense around Bragg conditions of the bulk crystal. Bulk elastic relaxations due to surface stress discontinuities at domain boundaries are responsible for this feature.

Interplay between atomic and mesoscopic order on gold vicinal surfaces.

Self-organization on Au(1,1,1) vicinal surfaces provides a unique opportunity to study the interplay between atomic and mesoscopic order. First, experimental results demonstrate the different interactions between steps and surface reconstruction on Au(1,1,1) vicinal surfaces. Depending on the step atomic structure, lines of discommensurations are found to be either parallel or perpendicular to the step edges.