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We present a general experimental concept for jitter-free pump and probe experiments at free electron lasers. By generating pump and probe pulse from one and the same X-ray pulse using an optical split-and-delay unit, we obtain a temporal resolution that is limited only by the X-ray pulse lengths. In a two-color X-ray pump and X-ray probe experiment with sub 70 fs temporal resolution, we selectively probe the response of orbital and charge degree of freedom in the prototypical functional oxide magnetite after photoexcitation. We find electronic order to be quenched on a time scale of (30 +/- 30) fs and hence most likely faster than what is to be expected for any lattice dynamics. Our experimental result hints to the formation of a short lived transient state with decoupled electronic and lattice degree of freedom in magnetite. The excitation and relaxation mechanism for X-ray pumping is discussed within a simple model leading to the conclusion that within the first 10 fs the original photoexcitation decays into low-energy electronic excitations comparable to what is achieved by optical pump pulse excitation. Our findings show on which time scales dynamical decoupling of degrees of freedom in functional oxides can be expected and how to probe this selectively with soft X-ray pulses. Results can be expected to provide crucial information for theories for ultrafast behavior of materials and help to develop concepts for novel switching devices. (C) 2018 Author(s).

We present a general experimental concept for jitter-free pump and probe experiments at free electron lasers. By generating pump and probe pulse from one and the same X-ray pulse using an optical split-and-delay unit, we obtain a temporal resolution that is limited only by the X-ray pulse lengths. In a two-color X-ray pump and X-ray probe experiment with sub 70 fs temporal resolution, we selectively probe the response of orbital and charge degree of freedom in the prototypical functional oxide magnetite after photoexcitation. We find electronic order to be quenched on a time scale of (30 +/- 30) fs and hence most likely faster than what is to be expected for any lattice dynamics. Our experimental result hints to the formation of a short lived transient state with decoupled electronic and lattice degree of freedom in magnetite. The excitation and relaxation mechanism for X-ray pumping is discussed within a simple model leading to the conclusion that within the first 10 fs the original photoexcitation decays into low-energy electronic excitations comparable to what is achieved by optical pump pulse excitation. Our findings show on which time scales dynamical decoupling of degrees of freedom in functional oxides can be expected and how to probe this selectively with soft X-ray pulses. Results can be expected to provide crucial information for theories for ultrafast behavior of materials and help to develop concepts for novel switching devices. (C) 2018 Author(s).

Ultrafast Magnetism I: International Conference UMC 2013 Strasbourg, France, October 28th - November 1st, 2013, Item does not contain fulltext, We employ time-resolved X-ray magnetic circular dichroism with fs time resolution to investigate the ultrafast, laser-driven dynamics of multi-sublattice materials, with both ferromagnetic and antiferromagnetic coupling. These measurements provide evidence for a demagnetization time that scales with the elemental magnetic moment and varies with the exchange interaction symmetry.

Contains fulltext : 169321.pdf (publisher's version ) (Open Access)

Ultrafast Magnetism I: International Conference UMC 2013 Strasbourg, France, October 28th - November 1st, 2013, Item does not contain fulltext

Ultrafast Magnetism I: International Conference UMC 2013 Strasbourg, France, October 28th - November 1st, 2013, Item does not contain fulltext, We employ time-resolved X-ray magnetic circular dichroism with fs time resolution to investigate the ultrafast, laser-driven dynamics of multi-sublattice materials, with both ferromagnetic and antiferromagnetic coupling. These measurements provide evidence for a demagnetization time that scales with the elemental magnetic moment and varies with the exchange interaction symmetry.

Contains fulltext : 169321.pdf (publisher's version ) (Open Access)

Ultrafast Magnetism I: International Conference UMC 2013 Strasbourg, France, October 28th - November 1st, 2013, Item does not contain fulltext

Ultrafast Magnetism I: International Conference UMC 2013 Strasbourg, France, October 28th - November 1st, 2013, Item does not contain fulltext, We employ time-resolved X-ray magnetic circular dichroism with fs time resolution to investigate the ultrafast, laser-driven dynamics of multi-sublattice materials, with both ferromagnetic and antiferromagnetic coupling. These measurements provide evidence for a demagnetization time that scales with the elemental magnetic moment and varies with the exchange interaction symmetry.

Irradiating a ferromagnet with a femtosecond laser pulse is known to induce an ultrafast demagnetization within a few hundred femtoseconds. Here we demonstrate that direct laser irradiation is in fact not essential for ultrafast demagnetization, and that electron cascades caused by hot electron currents accomplish it very efficiently. We optically excite a Au/Ni layered structure in which the 30 nm Au capping layer absorbs the incident laser pump pulse and subsequently use the X-ray magnetic circular dichroism technique to probe the femtosecond demagnetization of the adjacent 15 nm Ni layer. A demagnetization effect corresponding to the scenario in which the laser directly excites the Ni film is observed, but with a slight temporal delay. We explain this unexpected observation by means of the demagnetizing effect of a superdiffusive current of non-equilibrium, non-spin-polarized electrons generated in the Au layer.

FLASH has been a user facility since 2005, delivering radiation in the wavelength range between 7 and 47 nm using the SASE principle. After the present upgrade, the wavelength range is extended to 4.45 nm. With the third harmonic accelerating module in place to linearize the longitudinal phase space, the stability and reproducibility of the machine is substantially improved. The user requests for beam time by far exceeds the time available. In order to increase user beam time and to improve the radiation properties delivered to users, a major extension of the user facility called FLASH II has been proposed by DESY in collaboration with the HZB. FLASH II is a seeded FEL in the parameter range of FLASH. As logical continuation, the seeding with HHG which started with sFLASH will result in direct seeding. Because in the foreseeable future there will probably not be HHG seed lasers available at high repetition rates down to wavelengths of 4 nm, a cascaded HGHG scheme is proposed to produce short wavelengths. After a first design report, the project now enters its technical design phase. During this time, the FLASH beam parameters after the present upgrade 2009/2010 will be characterized and the present design will be re-evaluated and adjusted. In addition, start-to-end simulations will complete the simulations which have been performed so far, including a design of the extraction area.