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We investigate, both experimentally and theoretically, how the spectral distribution of laser accelerated carbon ions can be filtered by charge exchange processes in a double foil target setup. Carbon ions at multiple charge states with an initially wide kinetic energy spectrum, from 0.1 to 18 MeV, were detected with a remarkably narrow spectral bandwidth after they had passed through an ultrathin and partially ionized foil. With our theoretical calculations, we demonstrate that this process is a consequence of the evolution of the carbon ion charge states in the second foil. We calculated the resulting spectral distribution separately for each ion species by solving the rate equations for electron loss and capture processes within a collisional radiative model. We determine how the efficiency of charge transfer processes can be manipulated by controlling the ionization degree of the transfer matter.
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Direct acceleration of electrons in a coherent, intense light field is revealed by a remarkable increase of the electron number in the MeV energy range. Laser irradiation of thin polymer foils with a peak intensity of â¼1×10^{20} W/cm^{2} releases electron bunches along the laser propagation direction that are postaccelerated in the partly transmitted laser field. They are decoupled from the laser field at high kinetic energies, when a second foil target at an appropriate distance prevents their subsequent deceleration in the declining laser field. The scheme is established with laser pulses of high temporal contrast (10^{10} peak to background ratio) and two ultrathin polymer foils at a distance of 500 µm. 2D particle in cell simulations and an analytical model confirm a significant change of the electron spectral distribution due to the double foil setup, which leads to an amplification of about 3 times of the electron number around a peak at 1 MeV electron energy. The result verifies a theoretical concept of direct electron bunch acceleration in a laser field that is scalable to extreme acceleration potential gradients. This method can be used to enhance the density and energy spread of electron bunches injected into postaccelerator stages of laser driven radiation sources.
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An unprecedented increase of kinetic energy of laser accelerated heavy ions is demonstrated. Ultrathin gold foils have been irradiated by an ultrashort laser pulse at a peak intensity of 8×10^{19} W/ cm^{2}. Highly charged gold ions with kinetic energies up to >200 MeV and a bandwidth limited energy distribution have been reached by using 1.3 J laser energy on target. 1D and 2D particle in cell simulations show how a spatial dependence on the ion's ionization leads to an enhancement of the accelerating electrical field. Our theoretical model considers a spatial distribution of the ionization inside the thin target, leading to a field enhancement for the heavy ions by Coulomb explosion. It is capable of explaining the energy boost of highly charged ions, enabling a higher efficiency for the laser-driven heavy ion acceleration.
Asunto(s)
Iones Pesados , Rayos Láser , Modelos Teóricos , Aceleradores de Partículas , Oro/química , TermodinámicaRESUMEN
We present experimental studies on ion acceleration from ultrathin diamondlike carbon foils irradiated by ultrahigh contrast laser pulses of energy 0.7 J focused to peak intensities of 5x10(19) W/cm2. A reduction in electron heating is observed when the laser polarization is changed from linear to circular, leading to a pronounced peak in the fully ionized carbon spectrum at the optimum foil thickness of 5.3 nm. Two-dimensional particle-in-cell simulations reveal that those C6+ ions are for the first time dominantly accelerated in a phase-stable way by the laser radiation pressure.
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Two different laser energy absorption mechanisms at the front side of a laser-irradiated foil have been found to occur, such that two distinct relativistic electron beams with different properties are produced. One beam arises from the ponderomotively driven electrons propagating in the laser propagation direction, and the other is the result of electrons driven by resonance absorption normal to the target surface. These properties become evident at the rear surface of the target, where they give rise to two spatially separated sources of ions with distinguishable characteristics when ultrashort (40fs) high-intensity laser pulses irradiate a foil at 45 degrees incidence. The laser pulse intensity and the contrast ratio are crucial. One can establish conditions such that one or the other of the laser energy absorption mechanisms is dominant, and thereby one can control the ion acceleration scenarios. The observations are confirmed by particle-in-cell (PIC) simulations.
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Laser accelerated proton beams have been used for field characterization in expanding plasmas. The Thomson parabola spectrometer, as a charged particles analyzer, also allows precise measurement of the charged particles' trajectories. The proton's deflections by fast changing plasma fields can be measured with the new design of the Thomson parabola spectrometer and, therefore, it can be applied for proton deflectometry. It is shown that from resulting spectrograms the plasma field dynamics can be reconstructed with high temporal resolution. In a proof-of-principle experiment, a weakly relativistic plasma expansion is studied as an example.
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We report on a Paul-trap system with large access angles that allows positioning of fully isolated micrometer-scale particles with micrometer precision as targets in high-intensity laser-plasma interactions. This paper summarizes theoretical and experimental concepts of the apparatus as well as supporting measurements that were performed for the trapping process of single particles.
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A new design of an ion mass spectrometer for the laser-plasma particle diagnostic, which is capable to detect simultaneously also neutral particles, is described. The particles are detected with micro-channel-plate detector operating in a gated mode. This allows us to separate x-rays and energetic electrons from other stray plasma emissions, e.g., neutral particles, which hit the detector in the same place. The ion energies are measured with the spectrometer in energy intervals corresponding to their time-of-flight within the gating window. The latter also defines the energy interval of neutrals recorded with the same time-of-flight. The spectrum of neutral particles can be reconstructed by subsequently collecting different parts of the spectrum while applying different delays on the gate pulse. That separation-in-time technique (time-of-flight mass spectrometry) in combination with the spatially separating mass analyzer (ion mass spectrometer) is used for the neutral particles spectroscopy.
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The scenario of "electron-capture and -loss" was recently proposed for the formation of negative ion and neutral atom beams with MeV kinetic energies. However, it does not explain why the formation of negative ions in a liquid spray is much more efficient than with an isolated atom. The role of atomic excited states in the charge-exchange processes is considered, and it is shown that it cannot account for the observed phenomena. The processes are more complex than the single electron-capture and -loss approach. It is suggested that the shell effects in the electronic structure of the projectile ion and/or target atoms may influence the capture/loss probabilities.
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Our theoretical analysis reveals that tunnel ionization significantly modifies the electric field of few-cycle laser pulses within a single oscillation period. This subcycle self-modulation is predicted to result in phase matching, making high harmonic generation in the x-ray regime possible for the first time. Such a radiation source opens novel possibilities in the investigation of matter with x-ray techniques, such as time resolved x-ray diffraction and absorption.
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Using few-cycle-driven coherent laser harmonics, K-shell vacancies have been created in light elements, such as boron (E(B) = 188 eV) and carbon (E(B) = 284 eV), on a time scale of a few femtoseconds for the first time. The capability of detecting x-ray fluorescence excited by few-femtosecond radiation with an accuracy of the order of 1 eV paves the way for probing the evolution of the microscopic environment of selected atoms in chemical and biochemical reactions on previously inaccessible time scales (<100 fs) by tracing the temporal evolution of the "chemical shift" of peaks associated with inner-shell electronic transitions in time-resolved x-ray fluorescence and photoelectron spectra.
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An efficient acceleration of energetic ions is observed when small heavy-water droplets of approximately 20 microm diameter are exposed to ultrafast (approximately 40 fs) Ti:sapphire laser pulses of up to 10(19) W/cm2 intensity. Quantitative measurements of deuteron and neutron spectra were done, allowing one to analyze the outward and inward directed deuteron acceleration from the droplet. Neutron spectroscopy based on the D (d,n) fusion reaction was accomplished in four different spatial directions. The energy shifts of those fusion neutrons produced inside the exploding droplet reflect a remaining deuteron acceleration inside the irradiated droplet along the axis of the incident laser beam. The overall neutron yield of the microdroplets is relatively small as a result of the dominant outward directed acceleration of the deuterons with 1200 neutrons/shot. Relying on the "explosion-like" acceleration of such spherical droplet targets we have developed a spray target consisting of heavy-water microspheres with diameters of 150 nm . Both the high deuteron energies of up to 1 MeV resulting from the irradiation intensity of approximately 10(19) W/cm2 as well as the collisions between the deuterons and the surrounding spray delivered about one order of magnitude more neutrons than the single-droplet system. The approximately 6 x 10(3) neutrons per laser pulse from the spray can be attributed to an efficient deuteron release from a significantly smaller laser excited volume as from deuterium-cluster targets.
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Large Xe clusters (10(5)-10(6) atoms per cluster) have been irradiated with ultrashort (50 fs) and high-intensity ( approximately 2 x 10(18) W/cm(2)) pulses from a Ti:sapphire multi-TW laser at 800 nm wavelength. Scaling and absolute yield measurements of extreme ultraviolet (EUV) emission in a wavelength range between 7 and 15 nm in combination with cluster target characterization have been used for yield optimization. Maximum emission as a function of the backing pressure and a spatial emission anisotropy covering a factor of two at optimized yields is discussed with a simple model of the source geometry and EUV-radiation absorption. Circularly polarized laser light instead of linear polarization results in a factor of 2.5 higher emission in the 11 to 15 nm wavelength range. This indicates the initial influence of optical-field ionization for the interaction parameter range used and contrasts to collisional heating that seems to influence preferentially higher ionization. Absolute emission efficiency at 13.4 nm of up to 0.5% in 2pi sr and 2.2% bandwidth has been obtained.
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Rayos Láser , Rayos Ultravioleta , Xenón , Anisotropía , Iones , Fenómenos Físicos , Física , Presión , Factores de TiempoRESUMEN
We present a versatile and handy method allowing a thickness determination of freestanding thin plastic foils by its transmission characteristics in the extreme ultraviolet (EUV) spectrum. The method is based on a laser induced plasma source, emitting light in the EUV region, a compact double-mirror EUV monochromator operating at a fixed wavelength of 18.9 nm, and a CCD camera. The measurement delivers transmission values with a standard deviation of ΔT = 0.005 enabling foils thickness characterization with nm-accuracy at a given foil density and stoichiometric composition. Well characterized freestanding ultra-thin foils can be directly implemented in, e.g., high intensity laser matter experiments without further manipulation.
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We report on the absolute calibration of a microchannel plate (MCP) detector, used in conjunction with a Thomson parabola spectrometer. The calibration delivers the relation between a registered count numbers in the CCD camera (on which the MCP phosphor screen is imaged) and the number of ions incident on MCP. The particle response of the MCP is evaluated for positive, negative, and neutral particles at energies below 1 MeV. As the response of MCP depends on the energy and the species of the ions, the calibration is fundamental for the correct interpretation of the experimental results. The calibration method and arrangement exploits the unique emission symmetry of a specific source of fast ions and atoms driven by a high power laser.
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Liquid ethanol (C(2)H(5)OH) was used to generate a spray of sub-micron droplets. Sprays with different nozzle geometries have been tested and characterised using Mie scattering to find scaling properties and to generate droplets with different diameters within the spray. Nozzles having throat diameters of 470 µm and 560 µm showed generation of ethanol spray with droplet diameters of (180 ± 10) nm and (140 ± 10) nm, respectively. These investigations were motivated by the observation of copious negative ions from these target systems, e.g., negative oxygen and carbon ions measured from water and ethanol sprays irradiated with ultra-intense (5 × 10(19) W/cm(2)), ultra short (40 fs) laser pulses. It is shown that the droplet diameter and the average atomic density of the spray have a significant effect on the numbers and energies of accelerated ions, both positive and negative. These targets open new possibilities for the creation of efficient and compact sources of different negative ion species.
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Experimental demonstration of negative ion acceleration to MeV energies from sub-micron size droplets of water spray irradiated by ultra-intense laser pulses is presented. Thanks to the specific target configuration and laser parameters, more than 10(9) negative ions per steradian solid angle in 5% energy bandwidth are accelerated in a stable and reliable manner. To our knowledge, by virtue of the ultra-short duration of the emission, this is by far the brightest negative ion source reported. The data also indicate the existence of beams of neutrals with at least similar numbers and energies.
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Laser-driven ion acceleration is capable of generating ion beams of MeV energy exhibiting unique attributes such as ultralow emittance. Research is still focusing on fundamental laser-target interactions to control further beam attributes. In this Letter we present the observation of directional ion acceleration of irradiated spherical targets through proton imaging. This feature, together with an earlier observed quasimonoenergetic proton burst makes spherical targets extremely attractive candidates for high quality, high repetition rate sources of laser accelerated particles.
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Simultaneous detection of extreme ultra-violet (XUV) and ion emission along the same line of sight provides comprehensive insight into the evolution of plasmas. This type of combined spectroscopy is applied to diagnose laser interaction with a spray target. The use of a micro-channel-plate detector assures reliable detection of both XUV and ion signals in a single laser shot. The qualitative analysis of the ion emission and XUV spectra allows to gain detailed information about the plasma conditions, and a correlation between the energetic proton emission and the XUV plasma emission can be suggested. The measured XUV emission spectrum from water spray shows efficient deceleration of laser accelerated electrons with energies up to keV in the initially cold background plasma and the collisional heating of the plasma.
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We report on the generation and laser acceleration of bunches of energetic deuterons with a small energy spread at about 2 MeV. This quasimonoenergetic peak within the ion energy spectrum was observed when heavy-water microdroplets were irradiated with ultrashort laser pulses of about 40 fs duration and high (10(-8)) temporal contrast, at an intensity of 10(19) W/cm(2). The results can be explained by a simple physical model related to spatial separation of two ion species within a finite-volume target. The production of quasimonoenergetic ions is a long-standing goal in laser-particle acceleration; it could have diverse applications such as in medicine or in the development of future compact ion accelerators.