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Register a new userBent crystal spectrometer for both frequency and wavenumber resolved x-ray scattering at a seeded free-electron laser
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We present a cylindrically curved GaAs x-ray spectrometer with energy resolution $Delta E/E = 1.1cdot 10^{-4}$ and wave-number resolution of $Delta k/k = 3cdot 10^{-3}$, allowing plasmon scattering at the resolution limits of the Linac Coherent Light Source (LCLS) x-ray free-electron laser. It spans scattering wavenumbers of 3.6 to $5.2/$AA in 100 separate bins, with only 0.34% wavenumber blurring. The dispersion of 0.418~eV/$13.5,mu$m agrees with predictions within 1.3%. The reflection homogeneity over the entire wavenumber range was measured and used to normalize the amplitude of scattering spectra. The proposed spectrometer is superior to a mosaic HAPG spectrometer when the energy resolution needs to be comparable to the LCLS seeded bandwidth of 1~eV and a significant range of wavenumbers must be covered in one exposure.
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The resolution function of a spectrometer based on a strongly bent single crystal (bending radius of 10 cm or less) is evaluated. It is shown that the resolution is controlled by two parameters, (i) the ratio of the lattice spacing of the chosen reflection to the crystal thickness and (ii) a single parameter comprising crystal thickness, its bending radius, and anisotropic elastic constants of the chosen crystal. Diamond, due to its unique elastic properties, can provide notably higher resolution than silicon. The results allow to optimize the parameters of bent crystal spectrometers for the hard X-ray free electron laser sources.
We demonstrate that a mm-scale free electron laser can operate in the X-ray range, in the interaction between a moderately relativistic electron bunch, and a transverse high intensity optical lattice. The corrugated light-induced ponderomotive potential acts simultaneously as a guide and as a low-frequency wiggler, triggering stimulated Raman scattering. The gain law in the small signal regime is derived in a fluid approach, and confirmed from Particle-In-Cell simulations. We describe the nature of bunching, and discuss the saturation properties. The resulting all-optical Raman X-ray laser opens perspectives for ultra-compact coherent light sources up to the hard X-ray range.
Resonant elastic X-ray scattering has been widely employed for exploring complex electronic ordering phenomena, like charge, spin, and orbital order, in particular in strongly correlated electronic systems. In addition, recent developments of pump-probe X-ray scattering allow us to expand the investigation of the temporal dynamics of such orders. Here, we introduce a new time-resolved Resonant Soft X-ray Scattering (tr-RSXS) endstation developed at the Pohang Accelerator Laboratory X-ray Free Electron Laser (PAL-XFEL). This endstation has an optical laser (wavelength of 800 nm plus harmonics) as the pump source. Based on the commissioning results, the tr-RSXS at PAL-XFEL can deliver a soft X-ray probe (400-1300 eV) with a time resolution about ~100 fs without jitter correction. As an example, the temporal dynamics of a charge density wave on a high-temperature cuprate superconductor is demonstrated.
We propose a new scheme to generate high-brightness and temporal coherent soft x-ray radiation in a seeded free-electron laser. The proposed scheme is based the coherent harmonic generation (CHG) and superradiant principles. A CHG scheme is first used to generate coherent signal at ultra-high harmonics of the seed. This coherent signal is then amplified by a series of chicane-undulator modules via the fresh bunch and superradiant processes in the following radiator. Using a representative of realistic set of parameters, three-dimensional simulations have been carried out and the simulations results demonstrated that 10 GW-level ultra-short coherent radiation pulses in the water window can be achieved by using the proposed technique.
We demonstrate the structural sensitivity and accuracy of the standing wave technique at a high repetition rate free-electron laser, FLASH at DESY in Hamburg, by measuring the photoelectron yield from the surface SiO2 of Mo/Si multilayers. These experiments open up the possibility to obtain unprecedented structural information of adsorbate and surface atoms with picometer spatial accuracy and femtosecond temporal resolution. This technique will substantially contribute to a fundamental understanding of chemical reactions at catalytic surfaces and the structural dynamics of superconductors.
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