RESUMEN
We investigate the properties of a laser-plasma electron accelerator as a bright source of keV x-ray radiation. During the interaction, the electrons undergo betatron oscillations and from the carefully measured x-ray spectrum the oscillation amplitude of the electrons can be deduced which decreases with increasing electron energies. From the oscillation amplitude and the independently measured x-ray source size of (1.8±0.3) µm we are able to estimate the electron bunch diameter to be (1.6±0.3) µm.
Asunto(s)
Electrones , Rayos Láser , Aceleradores de Partículas , Dispersión de Radiación , Rayos XRESUMEN
Home-based soft X-ray time-resolved diffraction (TR-SXD) experiments with nanosecond time resolution (10 ns) and nanometer spatial resolution were carried out at a tabletop soft X-ray plasma source (2.7-5.9 nm). The investigated system was the lyotropic liquid crystal C(16)E(7)/paraffin/glycerol/formamide/IR 5. Usually, major changes in physical, chemical, and/or optical properties of the sample result from structural changes and shrinking morphology. Here, these effects occur as a consequence of the energy absorption in the sample upon optical laser excitation in the IR regime. The variations observed are integral intensity modulations and displacement in the Bragg diffraction angle. To follow the diffracted integral intensity changes, Patterson analysis was used, and the lattice parameter d variations have been followed by applying the Bragg diffraction law. The experimental intensity modulations occur on the nanosecond time scale, and they are assigned to photoinduced diffusion processes within the liquid crystalline phase. The structural response after photoexcitation is experimentally observed as an increase of the lattice constant by 0.5-1 A and is interpreted as a decrease of order in the liquid crystalline phase. This coincides with a reorientation to a photocreated liquid crystal lattice in the surface plane and with respect to the E-field vector of the laser light. The present studies emphasize the possibility of using TR-SXD techniques for studying the transient mechanical dynamics of nanosystems at the submicrosecond time scale.
Asunto(s)
Cristales Líquidos/química , Procesos Fotoquímicos , Cinética , Rayos Láser , Fenómenos Ópticos , Dispersión del Ángulo Pequeño , Difracción de Rayos XRESUMEN
We report on the fabrication of aluminum gallium nitride (AlGaN) Schottky-photodiode-based detectors. AlGaN layers were grown using metal-organic chemical vapor deposition (MOCVD) on Si(111) wafers. The diodes were characterized at a wavelength of 13.5 nm using a table-top extreme-ultraviolet (EUV) radiation source, consisting of a laser-produced xenon plasma and a Schwarzschild objective. The responsivity of the diodes was tested between EUV energies ranging from 320 nJ down to several picojoules. For low fluences, a linear responsivity of 7.14 mAs/J could be determined. Saturation starts at approximately 1 nJ, merging into a linear response of 0.113 mAs/J, which could be attributed to the photoeffect on the Au electrodes on top of the diode. Furthermore, degradation tests were performed up to an absolute dose of 3.3x10(19) photons/cm(2). AlGaN photodiodes were compared to commercially available silicon-based photodetectors. For AlGaN diodes, responsivity does not change even for the highest EUV dose, whereas the response of the Si diode decreases linearly to approximately 93% after 2x10(19) photons/cm(2).
RESUMEN
Home-based soft X-ray time-resolved scattering experiments with nanosecond time resolution (10 ns) and nanometer spatial resolution were carried out at a table top soft X-ray plasma source (2.2-5.2 nm). The investigated system was the lyotropic liquid crystal C(16)E(7)/paraffin/glycerol/formamide/IR 5. Usually, major changes in physical, chemical, and/or optical properties of the sample occur as a result of structural changes and shrinking morphology. Here, these effects occur as a consequence of the energy absorption in the sample upon optical laser excitation in the IR regime. The liquid crystal shows changes in the structural response within few hundred nanoseconds showing a time decay of 182 ns. A decrease of the Bragg peak diffracted intensity of 30% and a coherent macroscopic movement of the Bragg reflection are found as a response to the optical pump. The Bragg reflection movement is established to be isotropic and diffusion controlled (1 micros). Structural processes are analyzed in the Patterson analysis framework of the time-varying diffraction peaks revealing that the inter-lamellar distance increases by 2.7 A resulting in an elongation of the coherently expanding lamella crystallite. The present studies emphasize the possibility of applying TR-SXRD techniques for studying the mechanical dynamics of nanosystems.
Asunto(s)
Cristales Líquidos/química , Formamidas/química , Glicerol/química , Parafina/química , Dispersión del Ángulo Pequeño , Factores de Tiempo , Difracción de Rayos XRESUMEN
This article addresses the lateral organization of two-component lipid membranes deposited on a solid support with the addition of colloidal particles. The authors have applied synchrotron-based scanning transmission soft x-ray spectromicroscopy to image thin lipid layer patches with bound microspheres coated by a charged monolayer. The ability and current limits of scanning transmission x-ray spectromicroscopy to examine samples under physiologically relevant conditions in the presence of excess water have been tested. In particular, the authors have investigated a range of model lipids and have shown that these can be reproducibly identified from the near-edge x-ray absorption fine structure spectra at the carbon K absorption edge. Reference spectra were obtained based on a compact laser-driven plasma source, while the spectromicroscopy data were collected using synchrotron radiation at a lateral resolution of about 60 nm. The authors show that thin lipid layer sensitivity can indeed be reached under physiological conditions and that membrane colloid interaction as well as eventual lateral segregation of lipid components may be probed in the future by this technique.
RESUMEN
We present a laser driven soft x-ray source based on a novel solid argon filament. The continuously flowing micron-sized filament (diameter approximately 56 microm, flow speed approximately 5 mms) was used as a laser target in order to generate a plasma source of high brightness in the "water window" (2.2-4.4 nm) spectral range. The emission properties of the source were characterized in detail with respect to crucial parameters such as positional and energy stability using an extreme ultraviolet (XUV) sensitive pinhole camera and an XUV spectrometer. The results are compared with an argon plasma based on a gas puff target operated under the same experimental conditions showing an increase of the brilliance by a factor of 84. By changing the capillary geometry from a constant diameter to a convergent shape the flow speed of the filament was significantly increased up to 250 mms, facilitating the operation at higher repetition rates.