ABSTRACT
Refractive index gradients in materials or at material interfaces lead to x-ray diffraction. Interference of this radiation with adjacent x-ray waves causes phase contrast that can be used for imaging purposes if an x-ray source with sufficient spatial coherence is used. The imaging modality presented here uses hard x radiation diffracted at interfaces, but requires only little spatial coherence. We report experiments showing, first, that image contrast is not diminished by motional blurring, and second, that contrast can be increased by orders of magnitude relative to in-line x-ray phase-contrast imaging. These properties substantially broaden the applicability of phase-sensitive imaging to moving samples and very weak density gradients.
ABSTRACT
Ultrafast X-ray absorption near edge spectroscopy has been carried out for photo excited iron pentacarbonyl in ethanol with 2 picosecond resolution. A temporal resolution limited dissociation process was observed, followed by the formation of the mono-substituted complex Fe(CO)(4)EtOH within a few tens of picoseconds. The measurements have been carried out with a newly developed X-ray absorption instrument at station 7 ID-C of the Advanced Photon Source. The results show that single picosecond temporal resolution can be achieved at a synchrotron beam line.
Subject(s)
Ethanol/chemistry , Iron Carbonyl Compounds/chemistry , Ligands , X-Ray Absorption SpectroscopyABSTRACT
We report the generation of ultrashort, hard-x-ray pulses from a liquid mercury target irradiated by 5 kHz laser pulses. The new x-ray source is designed for time-resolved x-ray absorption spectroscopy as well as imaging applications. This marks the first laser-driven plasma x-ray source that continuously recycles the target material, facilitating maintenance-free operation. Theoretical calculations show mercury targets emit shorter x-ray pulses than targets of lighter elements under identical illumination and x-ray detection conditions.
