Transport studies of LPA electron beam towards the FEL amplification at COXINEL

Laser Plasma Acceleration (LPA) [1] is an emerging concept enabling to generate electron beams with high energy, high peak current and small transverse emittance within a very short distance. The use of LPA can be applied to the Free Electron Laser (FEL) [2] case in order to investigate whether it is suitable for the light amplification in the undulator. However, capturing and guiding of such beams to the undulator is very challenging, because of the large divergence and high energy spread of the electron beams at the plasma exit, leading to large chromatic emittances. A specific beam manipulation scheme was recently proposed for the COXINEL (Coherent X-ray source inferred from electrons accelerated by laser) setup, which makes an advantage from the intrinsically large chromatic emittance of such beams [3]. The electron beam transport is studied using two simulation codes: a SOLEIL in-house one and ASTRA [4]. The influence of the collective effects on the electron beam performance is also examined

Structure and Magnetic Properties of the Radical Cation Salt of a TTF-based NiII Complex

Chemical oxidation of a TTF-based NiII complex with I2 produces the corresponding radical cation salt 1, [Ni2Cl2(L)2](I3)2(I5)2(I2)(H2O)2(C4H8O)3, (L=4,5-bis(2-pyridylmethylsulfanyl)-4',5'-ethylenedithiotetrathiafulvalene). The results of magnetic susceptibility measurements show the occurrence of intramolecular magnetic exchange interactions in 1. The lack of close S···S contacts, confirmed by crystal structure analysis, results in an insulating behavio

Dithiinmaleimide Functionalized ET Derivatives: Syntheses, Characterization and X-ray Structure

Dithiinmaleimide (ethylenedithio)tetrathiafulvalene (1) and N-phenyldithiinmaleimide (ethylenedithio)tetrathiafulvalene (2) have been synthesized from bis(tetraethylammonium)bis(ethylenedithiotetrathiafulvalenyldithiolato)-zincate (3) in high yields. Their electrochemical properties were investigated by cyclic voltammetry (CV) measurements which show two reversible redox potentials of the tetrathiafulvalene (TTF) moiety and an irreversible reduction potential of the maleimide ring. The X-ray structure of 1 shows close S···S contacts in the range of the van der Waals radii (3.6 Å) and hydrogen bonds between the maleimide unite

Bond energy/eond order relationships for N-O linkages and a quantitative measure of ionicity: the rôle of nitro groups in hydrogen bonding

The nitro group is active in metabolic systems and can be found as an integral part of a number of useful curative drugs and many toxic substances. The basis for much of this activity is not fully understood. It is not necessarily caused directly by through-bond electronic effects but may also be due to direct H-bonding to nitro or to indirect interference by the nitro group with existing H-bonding. An unusual effect of a nitro substituent on kinetic results from urethane addition/elimination reactions (Scheme 1) has been ascribed to some form of self-association, which was neither specified nor quantified. To investigate self-association phenomena caused by a nitro group, a bond energy/bond order formula for N–O bonds has been developed and then used to interpret relative amounts of covalent and ionic contributions to total N–O bond energy. Calculated bond energies were then used to obtain enthalpies of formation for H-bonds to nitro groups in crystals and in solution. Similar results from solution data reveal that direct H-bonding to nitro is much weaker than in crystals, unless intramolecular H-bonding can occur. The results revealed that the 'self-association' effects observed for nitro substituents in urethanes (Scheme 1) were not caused by nitro participating directly in intermolecular bonding to NH of another urethane but by an indirect intramolecular action of the nitro group on pre-existing normal NH–O amide/amide type H-bonding

Toward a new hybrid proton conductor: lanthanum niobate layered perovskites as a source of tailorable surfaces

The modification of metal oxide surfaces with organic moieties has been widely studied as a method of preparing organic-inorganic hybrid materials for various applications. Among inorganic oxides, the ion-exchangeable layered perovskites [1], materials composed by perovskite-like slabs and intercalated cations, stimulated authors\u2019 interest in reason of some encouraging electronic and reactive properties. In particular it is well known that the interlayer surface of such materials in their protonated form can be easily functionalized with organic groups (such as alcohols [2-3] or organophosphonic acids [4]) thus allowing the production of stable hybrid materials with new electronic and reactive features. As a first step to design a new inorganic-organic hybrid proton conductor, a comprehensive theoretical investigation of the MLaNb2O7 (M=H, Li, Na, K, Rb and Cs) series of ion-exchangeable layered perovskite is presented. In particular, their structural and electronic properties have been investigated by periodic calculations in the framework of DFT. A general very good agreement with the available experimental data has been found. The protonated compound (HLaNb2O7) has been then functionalized with imidazole trying two different settings: in the first arrangement the molecule is adsorbed on the layered oxide exposing the interlayer surface, in the second the organic moiety is just put between two perovskites slabs. This latter model, including the effect of the confinement, allowed to better reproduce the experimental structural XRD data and 13C-NMR measurements of the hybrid system. [1] Schaak, R. E. and Mallouk T. E., Chem. Mat. 2002, 14, 1455-1471. [2] Takahashi S. et al., Inorg. Chem. 1995, 34, 5065-5069. [3] Suzuki H. et al., Chem. Mater. 2003, 15, 636-641. [4] Shimada, A. et al., Chem. Mat. 2009, 21, 4155-4162

Stability and Electronic Properties of TiO2 Nanostructures With and Without B and N Doping

We address one of the main challenges to TiO2-photocatalysis, namely band gap narrowing, by combining nanostructural changes with doping. With this aim we compare TiO2's electronic properties for small 0D clusters, 1D nanorods and nanotubes, 2D layers, and 3D surface and bulk phases using different approximations within density functional theory and GW calculations. In particular, we propose very small (R < 0.5 nm) but surprisingly stable nanotubes with promising properties. The nanotubes are initially formed from TiO2 layers with the PtO2 structure, with the smallest (2,2) nanotube relaxing to a rutile nanorod structure. We find that quantum confinement effects - as expected - generally lead to a widening of the energy gap. However, substitutional doping with boron or nitrogen is found to give rise to (meta-)stable structures and the introduction of dopant and mid-gap states which effectively reduce the band gap. Boron is seen to always give rise to n-type doping while depending on the local bonding geometry, nitrogen may give rise to n-type or p-type doping. For under coordinated TiO2 surface structures found in clusters, nanorods, nanotubes, layers and surfaces nitrogen gives rise to acceptor states while for larger clusters and bulk structures donor states are introduced

The ARC-EN-CIEL radiation sources

MOPC005International audienceThe ARC-EN-CIEL (Accelerator-Radiation for Enhanced Coherent Intense Extended Light) project proposes a panoply of light sources for the scientific community on a 1 GeV superconducting LINAC (phase 2) on which two ERL loops (1 and 2 GeV) are added in phase 3. LEL1 (200-1.5 nm), LEL2 (10-0.5 nm) and LEL4 (2-0.2 nm) are three kHz High Gain Harmonic Generation Free Electron Laser sources seeded with the High order Harmonics generated in Gas, with 100-30 FWHM pulses. A collaboration, which has been set-up with the SCSS Prototype Accelerator in Japan to test this key concept of ARC-EN-CIEL, has led to the experimental demonstration of the seeding with HHG and the observation up the 7th non linear harmonic with a seed at 160 nm. LEL3 (40-8 nm) installed on the 1 GeV loop is a MHz FEL oscillator providing higher average power and brilliance. In addition, in vacuum undulator spontaneous emission source extend the spectral range above 10 keV and intense THz radiation is generated by edge radiation of bending magnets. Optimisations and light sources characteristics are described

Presentation of the Smith-Purcell Experiment at SOLEIL

TUPC37 - Work supported by seed funding from Université Paris-Sud, program "Attractivité" and by the ANR under contract ANR-12-JS05-0003-01International audienceThe potential of Coherent Smith-Purcell radiation as a longitudinal bunch profile monitor has already been demonstrated and has recently been extended to the sub-picosecond range. As a critical step toward the construction of a single shot bunch profile monitor using Coherent Smith-Purcell radiation it is important to measure very accurately the distribution of such radiation. Optimum background suppression techniques need to be found and relatively cheap detectors suitable for the far infra-red need to be qualified. To performthese tasks a test stand has been installed at the end of the linac of the synchrotron SOLEIL. This test stand and the first results from its commissioning will be presented here

Evaluación de acolchados para el control de la flora arvense en un cultivo de tomate: dos años de resultados

En el presente proyecto se estudian alternativas al uso de acolchado plástico con polietileno, el cual es un residuo de difícil gestión tanto en producción hortícola ecológica como en convencional. Durante los años 2006 y 2007 se han llevado a cabo diez ensayos de campo en tomate de industria regado por goteo en cinco distintos lugares de España. Se han ensayado diferentes materiales biodegradables: dos plásticos biodegradables (Mater-Bi y Biofilm), un plástico oxobiodegradable (Enviroplast), dos papeles (papel negro Mimcord y marrón Saikraft), un acolchado de paja de cebada y dos testigos (sin desherbar y con control manual de las malas hierbas). Todas las películas fueron colocadas con máquina acolchadora, y los papeles requirieron un ajuste especial para evitar roturas. En todas las localidades y en ambos años el control de la flora arvense fue bueno o muy bueno para todos los acolchados, menos para la paja. Respecto al rendimiento de tomate, éste fue muy similar para todos los acolchados en ambos años, aunque ligeramente inferior que para el polietileno. En algunas localidades fue difícil mantener la paja en el suelo debido a su dispersión con el viento, mientras que en otras se mantuvo durante todo el ciclo. A pesar del peor control de la flora arvense, la paja dio buenos rendimientos en algunas localidades. El plástico oxobiodegradable mostró un comportamiento muy irregular entre localidades en cuanto a su degradación y cabe destacar la ausencia de degradación de la parte enterrada en todos los casos. Los plásticos biodegradables se degradaron de forma correcta cuando el cultivo ya cubría parte del suelo. El papel Mimcord fue más elástico permitiendo una más fácil colocación en el suelo pero es sensiblemente más caro que el marrón. En 2007 el rendimiento fue ligeramente menor para el papel marrón en 2007, posiblemente debido a que se trató de un año más frío. Los diferentes materiales biodegradables y el papel negro han sido los tratamientos más productivos y que mejor han controlado la flora arvense. Se concluye que existen alternativas técnicamente viables para sustituir el acolchado con polietileno en el cultivo de tomate de industria. No obstante, el elevado coste de la mayoría de estos materiales es el principal factor limitante para su adopción.Publishe