T. Sauvage
Centre national de la recherche scientifique
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Featured researches published by T. Sauvage.
Small | 2008
Orestis Faklaris; Damien Garrot; Vandana Joshi; Frédéric Druon; Jean-Paul Boudou; T. Sauvage; Patrick Georges; Patrick A. Curmi; F. Treussart
Diamond nanoparticles are promising photoluminescent probes for tracking intracellular processes, due to embedded, perfectly photostable color centers. In this work, the spontaneous internalization of such nanoparticles (diameter 25 nm) in HeLa cancer cells is investigated by confocal microscopy and time-resolved techniques. Nanoparticles are observed inside the cell cytoplasm at the single-particle and single-color-center level, assessed by time-correlation intensity measurements. Improvement of the nanoparticle signal-to-noise ratio inside the cell is achieved using a pulsed-excitation laser and time-resolved detection taking advantage of the long radiative lifetime of the color-center excited state as compared to cell autofluorescence. The internalization pathways are also investigated, with endosomal marking and colocalization analyses. The low colocalization ratio observed proves that nanodiamonds are not trapped in endosomes, a promising result in prospect of drug delivery by these nanoparticles. Low cytotoxicity of these nanoparticles in this cell line is also shown.
Surface & Coatings Technology | 2003
A. Moustaghfir; Eric Tomasella; S. Ben Amor; M. Jacquet; J. Cellier; T. Sauvage
Abstract Zinc oxide thin films were deposited on various substrates by sputtering from a ZnO target. The sputtering gas was obtained from an argon–oxygen mixture (95–5%), at 1 Pa pressure and using a r.f. power density of 0.89 W cm −2 . The structural and optical properties of ZnO deposits, submitted to an annealing treatment in the 373–673 K ranges are studied by X-ray diffraction (XRD) and UV-visible spectrometry. XRD measurements show that all the films are crystallised in the wurtzite phase and present a preferential orientation along the c -axis. Only one peak, corresponding to the (002) phase (2 θ≈ 34.4°), appears on the diffractograms. The crystallite size, the density and the O/Zn atomic ratio increases with the treatment temperature. These modifications influence the optical properties. The refractive index n , the absorption coefficient α and the optical gap E g , increase with the treatment temperature, and are sensitive to the oxygen incorporation.
Journal of Physics D | 2004
Pascal Brault; Amaël Caillard; Anne-Lise Thomann; Jacky Mathias; Christine Charles; Roderick Boswell; S. Escribano; J. Durand; T. Sauvage
Platinum is deposited into porous carbon materials relevant for fuel cell electrodes using plasma sputtering techniques. The resulting platinum concentration profile extends up to 2 µm into the porous carbon and is well fitted by a generalized stretched Gaussian function, which displays the non-thermal nature of the penetration process. Platinum deposits are observed to grow as clusters. On the outermost carbon particles, platinum nano-cluster sizes of 3.5 nm have been measured. In tests using actual PEM fuel cells, current densities as high as 1000 mA cm−2 have been obtained at 400 mV with 25 cm2 plasma electrodes. This compares favourably with commercially available electrodes but the present electrodes have a platinum density 4.5 times lower and hence can be considered to be significantly more efficient.
Optics Letters | 2008
Yannick Sonnefraud; Aurélien Cuche; Orestis Faklaris; Jean-Paul Boudou; T. Sauvage; Jean-François Roch; François Treussart; S. Huant
Diamond nanocrystals containing highly photoluminescent color centers are attractive, nonclassical, and near-field light sources. For near-field applications, the size of the nanocrystal is crucial, since it defines the optical resolution. Nitrogen-vacancy (NV) color centers are efficiently created by proton irradiation and annealing of a nanodiamond powder. Using near-field microscopy and photon statistics measurements, we show that nanodiamonds with sizes down to 25 nm can hold a single NV color center with bright and stable photoluminescence.
arXiv: Materials Science | 2007
Yannick Sonnefraud; Aurélien Cuche; Orestis Faklaris; Jean-Paul Boudou; T. Sauvage; Jean-François Roch; François Treussart; S. Huant
Diamond nanocrystals containing highly photoluminescent color centers are attractive, nonclassical, and near-field light sources. For near-field applications, the size of the nanocrystal is crucial, since it defines the optical resolution. Nitrogen-vacancy (NV) color centers are efficiently created by proton irradiation and annealing of a nanodiamond powder. Using near-field microscopy and photon statistics measurements, we show that nanodiamonds with sizes down to 25 nm can hold a single NV color center with bright and stable photoluminescence.
Journal of the European Optical Society: Rapid Publications | 2009
Orestis Faklaris; Damien Garrot; Vandana Joshi; Jean-Paul Boudou; T. Sauvage; Patrick A. Curmi; Fran C. Cois Treussart
Long term observations of photoluminescence at the single-molecule level were until recently very difficult, due to the photobleaching of organic fluorophore molecules. Although the inorganic semiconductor nanocrystals can overcome this difficulty showing very low photobleaching yield, they suffer from photoblinking. A new marker has been recently introduced, relying on diamond nanoparticles containing photoluminescent color centers. In this work we compare the photoluminescence of single quantum dots (QDs) to the one of nanodiamonds containing a single-color center. Contrary to other markers, photoluminescent nanodiamonds present a perfect photostability and no photoblinking. At saturation of their excitation, nanodiamonds photoluminescent intensity is only three times smaller that the one of QDs. Moreover, the bright and perfectly stable photoluminescence of nanodiamonds allows wide field observations of single nanoparticles motion. We demonstrate the possibility to follow the trajectory of such single particle in cells in culture and characterize its diffusion.
Journal of Physics D | 2003
Cong Wang; Pascal Brault; C. Zaepffel; J Thiault; A Pineau; T. Sauvage
W–Cu–W multilayer metallic coatings are designed and deposited by dc magnetron sputtering on an Fe substrate. Correlations between the deposition parameters, such as target power and Ar gas pressure, and the film characteristics are investigated. Especially, deposition parameters for a dense W–Cu multilayer coating are discussed. The coatings exhibit small grain sizes and a dense surface structure for high target power and low argon pressure, leading to dense and well adhesive films.
Journal of Nuclear Materials | 2003
S. Guilbert; T. Sauvage; H. Erramli; M.-F. Barthe; P. Desgardin; G. Blondiaux; C Corbel; J.P. Piron
AbstractThe behavior of helium implanted in sintered uranium dioxide disks has been investigated as a function of annealingtemperature. UO 2 disks have been implanted with 1 MeV 3 He at a nominal fluence of 5·10 16 3 Hecm 2 using a Van deGraaff accelerator. The 3 He(d,a) 1 H nuclear reaction analysis method was used to determine the helium depth profile inthe UO 2 disks. Partial flaking was observed after annealing at 500 C for local He concentration of 1 at.%. Afterannealing at 600 C flaking has affected the whole surface. The formation of helium bubbles is discussed. 2003 Elsevier B.V. All rights reserved. PACS: 66.30.h; 61.82.m; 81.05.Je 1. IntroductionThe release of fission gases, mostly Xe, from UO 2 and spent fuels has been extensively studied since themiddle of the 1960s [1–5]. The solubility of these gases isextremely low in UO 2 and, as a consequence, the gasatoms tend to precipitate into bubbles. In irradiatedfuels, a high density ( 10 17 cm 3 ) of small intragranularbubbles of about 2 nm uniformly distributed in thematrix are observed [6,7]. The size of the bubbles in-creases and the concentration decreases slightly withincreasing temperature and burnup. At higher burnupand/or temperatures a second bubble population is cre-ated with a larger mean diameter (10–20 nm) [7]. Theprecipitation of bubbles has also been demonstrated foruranium dioxide samples implanted with Kr and Xe evenat temperatures as low as 300–350 C [8,9].Fewer experiments have been performed on the be-havior of helium gas produced by alpha decay of acti-nides [10,11]. Yet the amount of helium produced afterirradiation are large in particular in the case of MOXfuels: the amount of helium produced in MOX (burnup47.5 GWd/tU) after 10000 years is evaluated at 6700cm
Journal of Applied Physics | 2000
S. Godey; T. Sauvage; E. Ntsoenzok; H. Erramli; M. F. Beaufort; J. F. Barbot; B. Leroy
We implanted n-type silicon with 1.6 MeV helium at fluences ranging from 1×1016 to 1×1017 He/cm2 while keeping a constant dose rate. These samples were then subjected to 800 °C annealing for 30 min. The results obtained by means of cross-sectional transmission electron microscopy indicate that the density of cavities is fluence dependent with homogeneous distribution of cavity sizes when fluences of 5×1016 and 1017 He/cm2 are used. The threshold fluence required to form cavities is found to be between 1 and 2×1016 He/cm2. For the 2×1016 He/cm2 dose, we observed loop punching induced by a concerted action of overpressurized bubbles, whereas He implants at doses of 5×1016 and 1×1017/cm2 lead to the formation of {311} defects. At the same time, non Rutherford elastic backscattering (NREBS) experiments using 2.5 MeV H+ provide the fraction of helium remaining in cavities after different annealing times at 800 °C. The NREBS data show a fast He release process for short annealing times (<2000 s). Then, the He a...
Surface & Coatings Technology | 2001
F. Fariaut; Chantal Boulmer-Leborgne; E. Le Menn; T. Sauvage; C Andreazza; Pascal Andreazza; C. Langlade
Abstract The excimer laser cementation process reported is developed to enhance the mechanical and chemical properties of aluminum alloys. It would be interesting to use aluminum alloys in the automotive industry widely because of their low density, corrosion resistance and good workability. The motor weight can be reduced by replacing usual materials such as iron–steel by light alloys treated to increase their wear resistance. Ceramic materials generally exhibit great strength, resistance to wear and oxidation. The use of laser beams allows surface treatment to be located at the parts strongly exposed to wear and friction. The surface undergoes a transformation leading to an increase in hardness without changing the dimensions of the piece, thus avoiding post machining after treatment. The laser process is especially suitable for environment protection as there is no pollution by chemical solvent or emanation. An excimer laser beam is focused onto the alloy surface in a cell containing 1 bar methane or propylene gas. A vapor plasma expands from the surface and a shockwave dissociates and ionizes the ambient gas. It is assumed that nitrogen or/and carbon from the plasma in contact with the surface penetrates into the depth. Thus, it is necessary to work with a sufficient laser fluence to create the plasma, but this fluence must be limited to prevent laser-induced surface roughness. The carbon concentration profiles are determined from Rutherford backscattering spectroscopy (RBS) and scanning electron microscopy (SEM). Crystalline quality is evidenced by grazing incidence X-ray diffraction (GIXD) technique. Transmission electron microscopy (TEM) gives the in-depth microstructure. The polycrystalline cemented layer obtained is several micrometers thick and composed of a pure composition (columnar microstructure) top layer (200–500-nm thick) standing on a diffusion layer (grains). Fretting test measurements exhibit an improvement of the surface mechanical behavior for some experimental conditions.