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O Stéphan

Publications and source records attributed to O Stéphan.

6 recordsLinked to original sources

Conjugated polymer/molten salt blend optimization.

Light-emitting electrochemical cells with low current threshold can be realized through mixing conjugated polymers and molten salts. Current drive capability is proportional to the overall interface perimeter of the planar, discotic molten salt domains inserted into the polymer matrix. Electric force microscopy indicates that this interface perimeter exhibits a specific dependence on the molten salt content in the active layer, with a well-defined maximum. We show that this maximum corresponds to an optimal current drive.

Fluorides↗

Electron energy loss spectroscopy measurement of the optical gaps on individual boron nitride single-walled and multiwalled nanotubes.

Spatially resolved electron energy loss spectroscopy experiments have been performed in an electron microscope on several individual boron nitride (BN) single-, double-, and triple-walled nanotubes, whose diameters and number of shells have been carefully measured. In the low-loss region (from 2 to 50 eV) the spectra have been analyzed within the framework of the continuum dielectric theory, leading to the conclusion of a weak influence of out-of-plane contribution to the dielectric response of the tubes. The gap has been measured to be independent of the nanotubes geometry, and close to the in-plane gap value of hexagonal BN (5.8+/-0.2 eV).

Journal Article↗

Nucleation and growth of single-walled nanotubes: the role of metallic catalysts.

We present a review of experimental and theoretical results on the nucleation and growth of single-walled nanotubes, with particular emphasis on the growth of nanotube bundles emerging from catalyst particles obtained from evaporation-based elaboration techniques. General results are first discussed. Experiments strongly suggest a root-growth process in which carbon, dissolved at high temperatures in catalytic particles, segregates at the surface at lower temperatures to form tube embryos and finally nanotubes through a nucleation and growth process. A theoretical analysis of the reasons carbon does not always form graphene sheets to wrap the particles suggests analogies with other surface or interface instabilities, in particular, with those found in epitaxial growth. In the second part, detailed experimental results for nickel-rare earth metal catalysts are presented. By using various electron microscopy techniques, it is shown that carbon and the rare earth metal co-segregate at the surface of the particle and form carbide platelets, providing nucleation sites for nanotubes growing in directions perpendicular to the surface. A simple theoretical model is then presented in which the role of the rare earth metal is just to transfer electrons from metal to carbon. The graphene sheet is shown to become unstable; pentagons and heptagons are favored, which can explain the occurrence of local curvatures and of tube embryos. Finally, a brief discussion of some recent atomistic models is given.

Carbon↗

Experimental evidence of surface-plasmon coupling in anisotropic hollow nanoparticles.

We report on the investigation of surface-plasmon excitation of anisotropic WS(2) hollow nanoparticles in a near-field geometry by means of a scanning transmission electron microscope. The shell thickness influence on the electron-energy-loss-spectroscopy spectra is experimentally observed and is analyzed within a classical dielectric formalism. As for the isotropic case, we evidence one symmetric (tangential) and one antisymmetric (radial) mode. We point out the intriguing fact that, for the anisotropic case, one can relate these modes to the interband transition of the in-plane component of the dielectric tensor and to the bulk-plasmon energy of the out-of-plane component.

Journal Article↗

2,2'-Bi(9,9-dihexylfluorene).

The central part of the title molecule, C(50)H(66), is planar, all the rings being in the same plane; the lateral chains are also planar (excluding H atoms), almost perpendicular to the ring plane and grafted on the same side of the molecule. The molecule has nearly a mirror plane, perpendicular to the central C-C bond, instead of the centre of symmetry expected. The orientation of the plane of the rings is approximately 45 degrees from the unit-cell b axis, so that neighbouring molecules are essentially perpendicular.

Journal Article↗