Deep red luminescent hybrid copolymer materials with high transition metal cluster content

Accepted 04 Dec 2013International audienceThe hybrid strategy is a powerful approach to design functional materials by combining inorganic dyes with an organic matrix. However, introducing high contents of inorganic species within the hybrid material is a real challenge that requires a perfect balance between the interactions of both components to avoid mainly phase segregation problems. Based on our demonstration on an anionic molybdenum cluster, we present a general method to introduce high contents of such class of nanometre sized inorganic molecular deep red dyes in a polymer matrix. Our strategy exploits the physical interactions between the organic and inorganic parts of the hybrid material and allows a high cluster rate to be introduced (up to 50 wt%) in the polymer matrix. The resulting hybrids are remarkably stable even after several months of ageing. Moreover, the Mo clusters maintain their intrinsic deep red luminescence properties while the polymer organic matrix fully maintains its processability, thanks to the di-anionic character of the Mo6 clusters. Such materials show promising prospects in applications needing deep red emitters

Preparation of nitrogen doped zinc oxide nanoparticles and thin films by colloidal route and low temperature nitridation process

International audienceNitrogen doped zinc oxide (ZnO) nanoparticles have been synthesized using a colloidal route and low temperature nitridation process. Based on these results, 200 nm thick transparent ZnO thin films have been prepared by dip-coating on SiO2 substrate from a ZnO colloidal solution. Zinc peroxide (ZnO2) thin film was then obtained after the chemical conversion of a ZnO colloidal thin film by H2O2 solution. Finally, a nitrogen doped ZnO nanocrystalline thin film (ZnO:N) was obtained by ammonolysis at 250°C. All the films have been characterized by scanning electron microscopy, X-ray diffraction, X-Ray photoelectron spectroscopy and UV-Visible transmittance spectroscopy

Resonance Raman Spectroscopy of extreme nanowires and other 1D systems

This paper briefly describes how nanowires with diameters corresponding to 1 to 5 atoms can be produced by melting a range of inorganic solids in the presence of carbon nanotubes. These nanowires are extreme in the sense that they are the limit of miniaturization of nanowires and their behavior is not always a simple extrapolation of the behavior of larger nanowires as their diameter decreases. The paper then describes the methods required to obtain Raman spectra from extreme nanowires and the fact that due to the van Hove singularities that 1D systems exhibit in their optical density of states, that determining the correct choice of photon excitation energy is critical. It describes the techniques required to determine the photon energy dependence of the resonances observed in Raman spectroscopy of 1D systems and in particular how to obtain measurements of Raman cross-sections with better than 8% noise and measure the variation in the resonance as a function of sample temperature. The paper describes the importance of ensuring that the Raman scattering is linearly proportional to the intensity of the laser excitation intensity. It also describes how to use the polarization dependence of the Raman scattering to separate Raman scattering of the encapsulated 1D systems from those of other extraneous components in any sample

BEDT-TTF organic superconductors: the entangled role of phonons

We calculate the lattice phonons and the electron-phonon coupling of the organic superconductor \kappa-(BEDT-TTF)_2 I_3, reproducing all available experimental data connected to phonon dynamics. Low-frequency intra-molecular vibrations are strongly mixed to lattice phonons. Both acoustic and optical phonons are appreciably coupled to electrons through the modulation of the hopping integrals (e-LP coupling). By comparing the results relevant to superconducting \kappa- and \beta-(BEDT-TTF)_2 I_3, we show that electron-phonon coupling is fundamental to the pairing mechanism. Both e-LP and electron-molecular vibration (e-MV) coupling are essential to reproduce the critical temperatures. The e-LP coupling is stronger, but e-MV is instrumental to increase the average phonon frequency.Comment: 4 pages, including 4 figures. Published version, with Ref. 17 corrected after publicatio

Opportunities for polymer-based nanowires in optoelectronics and nanophotonics

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Opportunities for polymer-based nanowires in optoelectronics and nanophotonics

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Transition Metal Cluster Compounds: Luminescence and Design of (nano)Composites

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Polymer-Based Nanowires and Nanotubes: nanosources, wave-guiding

International audienceOne-dimensional polymer-based nano-structures such as nanowires (NWs) and nanotubes (NTs) are nowadays intensively investigated since they promote enhanced properties, as well as new paradigms for electronic, optical, optoelectronic, and photonic devices. Here, we propose a review of recent developments achieved in our group with collaborations on polymer based nanowires and nanotubes. Various polymer based NWs and NTs were synthesized by template strategies with advanced architectures designed for improving their functionality (waveguiding, color control of photoluminescence, photoconductivity and mechanical reinforcement,…). Both conjugated polymers (CPs) and photoresists containing photo-active species (transition metal compound clusters, single-walled-carbon nanotubes SWCNTs) were involved. The focus is made on the emerging strategies for understanding and controlling the behavior of charges, excitons and photons, as well as light propagation in sub-wavelength nanostructures