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

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

Open-communication project : a case study of its development and implementation as a strategy for self-renewal of an urban junior high school.

EducationDoctor of Education (Ed.D.

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

Phase space analysis of velocity bunched beams

Peak current represents a key demand for new generation electron beam photoinjectors. Many beam applications, such as free electron laser, inverse Compton scattering, terahertz radiation generation, have efficiencies strongly dependent on the bunch length and current. A method of beam longitudinal compression (called velocity bunching) has been proposed some years ago, based on beam longitudinal phase space rotation in a rf field potential. The control of such rotation can lead to a compression factor in excess of 10, depending on the initial longitudinal emittance. Code simulations have shown the possibility to fully compensate the transverse emittance growth during rf compression, and this regime has been experimentally proven recently at SPARC. The key point is the control of transverse beam plasma oscillations, in order to freeze the emittance at its lowest value at the end of compression. Longitudinal and transverse phase space distortions have been observed during the experiments, leading to asymmetric current profiles and higher final projected emittances. In this paper we discuss in detail the results obtained at SPARC in the regime of velocity bunching, analyzing such nonlinearities and identifying the causes. The beam degradation is discussed, both for slice and projected parameters. Analytical tools are derived to experimentally quantify the effect of such distortions on the projected emittanc

Resonant Lifetime of Core-Excited Organic Adsorbates from First Principles

We investigate by first-principles simulations the resonant electron-transfer lifetime from the excited state of an organic adsorbate to a semiconductor surface, namely isonicotinic acid on rutile TiO$_2$(110). The molecule-substrate interaction is described using density functional theory, while the effect of a truly semi-infinite substrate is taken into account by Green's function techniques. Excitonic effects due to the presence of core-excited atoms in the molecule are shown to be instrumental to understand the electron-transfer times measured using the so-called core-hole-clock technique. In particular, for the isonicotinic acid on TiO$_2$(110), we find that the charge injection from the LUMO is quenched since this state lies within the substrate band gap. We compute the resonant charge-transfer times from LUMO+1 and LUMO+2, and systematically investigate the dependence of the elastic lifetimes of these states on the alignment among adsorbate and substrate states.Comment: 24 pages, 6 figures, to appear in Journal of Physical Chemistry

BEEHOPE: um projeto de conservação das subespécies nativas de abelha da Europa Ocidental (linhagem M) à escala Europeia

O projeto BEEHOPE, com o título original “Honeybee conservation centres in western Europe - an innovative strategy using sustainable beekeeping to reduce honeybee decline”, foi um dos 10 aprovados na área da biodiversidade do 5º concurso transnacional (2013-2014) BiodivErsA/FACCE-JPI (http://www.biodiversa.org/766), subordinado ao tema “Promover sinergias e reduzir o compromisso entre o abastecimento de alimentos, biodiversidade e serviços dos ecossistemas”. A diversidade nativa das populações de abelha melífera (Apis mellifera) da linhagem da Europa ocidental (M) tem vindo a ser crescentemente ameaçada pela introdução massiva de colónias da linhagem da Europa oriental (C, onde se incluem as subespécies A. m. ligustica, A. m. carnica, A. m. macedónica etc.), e também por outros fatores bióticos (Varroa e vírus associados, Nosema etc.) e abióticos (pesticidas, perda e fragmentação de habitat, alterações climáticas etc.). É neste contexto que surge o projeto BEEHOPE, o qual tem por objetivo último contribuir para a conservação da diversidade genética das populações de abelha melífera da linhagem M.info:eu-repo/semantics/publishedVersio