1,617 research outputs found

    CROSS SECTIONS FOR SCATTERING OF ELECTRONS ON BF3

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    We calculate cross sections for elastic scattering and electronic excitation of BF3 molecules by low energy electrons. The R-Matrix code Quantemol-N has been used for calculations. The cross sections indicate the presence of a shape resonance of symmetry B-1 (A(2)'' in D-3h) at around 4.5 eV

    Modelling radiation emission in the transition from the classical to the quantum regime

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    An emissivity formula is derived using the generalised Fermi-Weizacker-Williams method of virtual photons which accounts for the recoil the charged particle experiences as it emits radiation. It is found that through this derivation the formula obtained by Sokolov et al using QED perturbation theory is recovered. The corrected emissivity formula is applied to nonlinear Thomson scattering scenarios in the transition from the classical to the quantum regime, for small values of the nonlinear quantum parameter \chi. Good agreement is found between this method and a QED probabilistic approach for scenarios where both are valid. In addition, signatures of the quantum corrections are identified and explored.Comment: 11 pages, 4 figures, submitted for publicatio

    Table-top laser-based proton acceleration in nanostructured targets

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    The interaction of ultrashort, high intensity laser pulses with thin foil targets leads to ion acceleration on the target rear surface. To make this ion source useful for applications, it is important to optimize the transfer of energy from the laser into the accelerated ions. One of the most promising ways to achieve this consists in engineering the target front by introducing periodic nanostructures. In this paper, the effect of these structures on ion acceleration is studied analytically and with multidimensional particle-in-cell simulations.Weassessed the role of the structure shape, size, and the angle of laser incidence for obtaining the efficient energy transfer. Local control of electron trajectories is exploited to maximize the energy delivered into the target. Based on our numerical simulations, we propose a precise range of parameters for fabrication of nanostructured targets, which can increase the energy of the accelerated ions without requiring a higher laser intensity.This work has been partially supported by the Xunta de Galicia/FEDER under contract Agrup2015/11 (PC034) and by MINECO under contracts MAT2015-71119-R and FIS2015-71933-REDT. The authors would like to acknowledge the OSIRIS Consortium, consisting of UCLA and IST (Lisbon, Portugal) for the use of OSIRIS, for providing access to the OSIRIS framework. M Blanco also thanks the Ministry of Education of the Spanish government for the FPU fellowship. Camilo Ruiz also thanks MINECO project FIS2016-75652-P M Vranic acknowledges the support of ERC-2010-AdG Grant 267841 and LASERLAB-EUROPE IV—GA No. 654148. Simulations were performed at the Accelerates cluster (Lisbon, Portugal)S

    Phase Control of Nonlinear Breit-Wheeler Pair Creation

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    Electron-positron pair creation occurs throughout the universe in the environments of extreme astrophysical objects, such as pulsar magnetospheres and black hole accretion disks. The difficulty of emulating these environments in the laboratory has motivated the use of ultrahigh-intensity laser pulses for pair creation. Here we show that the phase offset between a laser pulse and its second harmonic can be used to control the relative transverse motion of electrons and positrons created in the nonlinear Breit-Wheeler process. Analytic theory and particle-in-cell simulations of a head-on collision between a two-color laser pulse and electron beam predict that with an appropriate phase offset, the electrons will drift in one direction and the positrons in the other. The resulting current may provide a collective signature of nonlinear Breit-Wheeler, while the spatial separation resulting from the relative motion may facilitate isolation of positrons for subsequent applications or detection.Comment: 8 pages, 5 figure

    Laser absorption via quantum electrodynamics cascades in counter propagating laser pulses

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    A model for laser light absorption in electron–positron plasmas self-consistently created via QED cascades is described. The laser energy is mainly absorbed due to hard photon emission via nonlinear Compton scattering. The degree of absorption depends on the laser intensity and the pulse duration. The QED cascades are studied with multi-dimensional particle-in-cell simulations complemented by a QED module and a macro-particle merging algorithm that allows to handle the exponential growth of the number of particles. Results range from moderate-intensity regimes (~ 10 PW) where the laser absorption is negligible to extreme intensities (>100 PW) where the degree of absorption reaches 80%. Our study demonstrates good agreement between the analytical model and simulations. The expected properties of the hard photon emission and the generated pair-plasma are investigated, and the experimental signatures for near-future laser facilities are discussed.info:eu-repo/semantics/submittedVersio

    Seeded QED cascades in counterpropagating laser pulses

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    The growth rates of seeded QED cascades in counterpropagating lasers are calculated with first-principles two-and three-dimensional QED-PIC (particle-in-cell) simulations. The dependence of the growth rate on the laser polarization and intensity is compared with analytical models that support the findings of the simulations. The models provide insight regarding the qualitative trend of the cascade growth when the intensity of the laser field is varied. A discussion about the cascade's threshold is included, based on the analytical and numerical results. These results show that relativistic pair plasmas and efficient conversion from laser photons to. rays can be observed with the typical intensities planned to operate on future ultraintense laser facilities such as ELI or Vulcan.info:eu-repo/semantics/submittedVersio

    QED vs. classical radiation reaction in the transition regime

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    We focus our analysis in the properties of an electron beam during/after collision with an intense pulse. The additional energy spread introduced by the stochastic nature of QED emission can be balanced by the average energy loss leading to overall energy spread reduction even in the QED regime.info:eu-repo/semantics/publishedVersio

    Novel therapeutic targets in salivary duct carcinoma uncovered by comprehensive molecular profiling.

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    Salivary duct carcinoma (SDC) is a rare, aggressive salivary gland malignancy, which often presents at an advanced stage. A proportion of SDC are characterized by HER2 amplification and/or overexpression of androgen receptor (AR), which could be targeted in a subset of patients, but the presence of AR splice variant-7 (AR-V7) in some SDC cases could result in resistance to anti-androgen therapy. We evaluated a cohort of 28 cases of SDC for potentially targetable biomarkers and pathways using immunohistochemistry (IHC) and next-generation sequencing (DNA and RNA) assays. Pathogenic genetic aberrations were found in all but 1 case and affected TP53 (n = 19), HRAS (n = 7), PIK3CA, ERBB2 (HER2), and NF1 (n = 5 each); KMT2C (MLL3) and PTEN (n = 3 each); BRAF (p.V600E), KDM5C and NOTCH1 (n = 2 each). Androgen receptor was expressed in all cases and 13 of 27 harbored the AR-V7 splice variant (including a case without any other detectable genetic alteration). HER2 IHC was expressed in 11 of 28 cases. The majority of SDC cases had no biomarkers predictive of immunotherapy response: 5 cases exhibited low (1%-8%) programmed death ligand 1 (PD-L1) expression in tumor cells, 2 cases exhibited elevated TMB, and no samples exhibited microsatellite instability. Notably, the pre-treatment biopsies from 2 patients with metastatic disease, who demonstrated clinical responses to anti-androgen therapy, showed AR expression and no AR splice variants. We conclude that comprehensive molecular profiling of SDCs can guide the selection of patients for targeted therapies involving AR, HER2, PD-L1, mitogen-activated protein kinase, and PIK3CA pathways
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