Sébastien Sorgues

Modification of TiO2 by Bimetallic Au-Cu Nanoparticles for Wastewater Treatment

Au, Cu and bimetallic Au-Cu nanoparticles were synthesized on the surface of commercial TiO2 compounds (P25) by reduction of the metal precursors with tetrakis (hydroxymethyl) phosphonium chloride (THPC) (0.5 % in weight). The alloyed structure of Au-Cu NPs was confirmed by HAADF-STEM, EDS, HRTEM and XPS techniques. The photocatalytic properties of the modified TiO2 have been studied for phenol photodegradation in aqueous suspensions under UV-visible irradiation. The modification by the metal nanoparticles induces an increase in the photocatalytic activity. The highest photocatalytic activity is obtained with Au-Cu/TiO2 (Au/Cu 1:3). Their electronic properties have been studied by time resolved microwave conductivity (TRMC) to follow the charge-carrier dynamics. TRMC measurements show that the TiO2 modification with Au, Cu and Au-Cu nanoparticles plays a role in charge-carrier separations increasing the activity under UV-light. Indeed, the metal nanoparticles act as a sink for electron, decreasing the charge carrier recombination. The TRMC measurements show also that the bimetallic Au-Cu nanoparticles are more efficient in electron scavenging than the monometallic Au and Cu ones.

Photocatalysis with Polyoxometalates Associated to Porphyrins under Visible Light: An Application of Charge Transfer in Electrostatic Complexes

Absorption spectrum of derived Dawson sandwich polyoxometalates (POM) [M(4)(H(2)O)(2)(P(2)W(15)O(56))(2)](n-) with n = 16 for M = Zn(II), Ni(II), and n = 12 for M = Fe(III) have been extended in the visible range forming electrostatic complexes with a chromophore, the zinc tetracationic porphyrin [ZnTMePyP](4+). Formation of such complexes was followed by steady-state absorption and luminescence spectroscopies. The electrostatic complexation gives in all cases a strong, neutral, and nonluminescent complex. A charge transfer between the two units was shown by transient absorption spectroscopy. Upon a visible excitation of the porphyrin subunit, an electron transfer from the porphyrin to the POM occurs and imparts it a catalytic activity. This has been demonstrated studying a model reaction such as the reduction of silver cations leading to nanoparticles. In all cases, the reduction of the silver cations takes place. We showed that the catalytic activity depends of the nature of the metal of the tetraoxometallic central cluster of the Dawson sandwich POM.

Picosecond pulse radiolysis of the liquid diethyl carbonate.

The diethyl carbonate, DEC, is an ester that is used as a solvent in Li-ion batteries, but its behavior under ionizing radiation was unknown. The transient optical absorption spectra, the decay kinetics, and the influence of various scavengers have been studied by using the picosecond laser-triggered electron accelerator ELYSE. In neat DEC, the intense near-IR (NIR) absorption spectrum is assigned to the solvated electron. It is overlapped in the visible range by another transient but longer-lived and less intense band that is assigned to the oxidized radical DEC(-H). The solvated electron molar absorption coefficients and radiolytic yield evolution from 25 ps, the geminate recombination kinetics, and the rate constants of electron transfer reactions to scavengers are determined. The radiolytic mechanism, indicating a certain radioresistance of DEC, is compared with that for other solvents.

Influence of Nitrogen Doping on Device Operation for TiO2-Based Solid-State Dye-Sensitized Solar Cells: Photo-Physics from Materials to Devices

Solid-state dye-sensitized solar cells (ssDSSC) constitute a major approach to photovoltaic energy conversion with efficiencies over 8% reported thanks to the rational design of efficient porous metal oxide electrodes, organic chromophores, and hole transporters. Among the various strategies used to push the performance ahead, doping of the nanocrystalline titanium dioxide (TiO2) electrode is regularly proposed to extend the photo-activity of the materials into the visible range. However, although various beneficial effects for device performance have been observed in the literature, they remain strongly dependent on the method used for the production of the metal oxide, and the influence of nitrogen atoms on charge kinetics remains unclear. To shed light on this open question, we synthesized a set of N-doped TiO2 nanopowders with various nitrogen contents, and exploited them for the fabrication of ssDSSC. Particularly, we carefully analyzed the localization of the dopants using X-ray photo-electron spectroscopy (XPS) and monitored their influence on the photo-induced charge kinetics probed both at the material and device levels. We demonstrate a strong correlation between the kinetics of photo-induced charge carriers probed both at the level of the nanopowders and at the level of working solar cells, illustrating a direct transposition of the photo-physic properties from materials to devices.

Observation and decay of free and ligated metalloporphyrins in the gas phase

A soft desorption technique has been tested in order to vaporize metalloporphyrins in a supersonic jet and study their energetics and dynamics in the gas phase at low temperatures. Several metalloporphyrins: ZnTPP, NiTPP, CoTPP and ligated RuTPP–CO have been detected by resonant 2 photon ionization. ZnTPP was observed with high sensitivity owing to its long S1 lifetime, while the transition metal porphyrins displayed less intense ion yields due to short excited state lifetimes. The ligated ruthenium complex could be observed intact and femtosecond excitation at 400 nm revealed the ultrashort excited state dissociation of the ruthenium metalloporphyrin.

Versatile Wafer-Scale Technique for the Formation of Ultrasmooth and Thickness-Controlled Graphene Oxide Films Based on Very Large Flakes

We present a new strategy to form thickness-adjusted and ultrasmooth films of very large and unwrinkled graphene oxide (GO) flakes through the transfer of both hemispherical and vertical water films stabilized by surfactants. With its versatility in terms of substrate type (including flexible organic substrates) and in terms of flake density (from isolated flakes to continuous and multilayer films), this wafer-scale assembly technique is adapted to a broad range of experiments involving GO and rGO (reduced graphene oxide). We illustrate its use through the evaluation of transparent rGO electrodes.

Kinetics study of the solvated electron decay in THF using laser-synchronised picosecond electron pulse

Abstract Picosecond pulse radiolysis of neat tetrahydrofuran (THF) shows a fast decay of the solvated electron within 2.5ns. The decay of the solvated electron observed at 790nm is because of spur reaction. A numerical simulation using time dependent Smoluchowski equation containing a sink term with a distance dependent reaction rate is used to fit the pulse-probe data and shows that the geminate reaction can proceed at long distance in this low polar solvent.