Here, we use x-rays to create and probe quantum coherence in the photoionized amino acid glycine. The outgoing photoelectron leaves behind the cation in a coherent superposition of quantum mechanical eigenstates. Delayed x-ray pulses track the induced coherence through resonant x-ray absorption that induces Auger decay and by photoelectron emission from sequential double photoionization. Sinusoidal temporal modulation of the detected signal at early times (0 to 25 fs) is observed in both measurements. Advanced ab initio many-electron simulations allow us to explain the first 25 fs of the detected coherent quantum evolution in terms of the electronic coherence. In the kinematically complete x-ray absorption measurement, we monitor its dynamics for a period of 175 fs and observe an evolving modulation that may implicate the coupling of electronic to vibronic coherence at longer time scales. Our experiment provides a direct support for the existence of long-lived electronic coherence in photoionized biomolecules.

Ultrafast X-ray spectroscopies require flexible X-ray properties together with high temporal and spectral resolution. Here, we demonstrate simultaneous sub-20 fs and sub-eV resolutions for pump/probe experiments, without the need for additional photon arrival-time monitors.

Self-amplified spontaneous emission (SASE) pulses delivered by free electron lasers (FELs) are inherently fluctuating sources; each pulse varies in energy, duration, arrival time and spectral shape. Therefore, there is strong demand for a full characterization of the properties of SASE radiation, which will facilitate more precise interpretation of the experimental data taken at SASE FELs. In this paper, we present an investigation into the fluctuations of pulse duration, spectral distribution, arrival time and pulse energy of SASE XUV pulses at FLASH, both on a shot-to-shot basis and on average over many pulses. With the aid of simulations, we derived scaling laws for these parameters and disentangled the statistical SASE fluctuations from accelerator-based fluctuations and measurement uncertainties.

X-ray absorption near-edge structure (XANES) spectroscopy provides element specificity and is a powerful experimental method to probe local unoccupied electronic structures. In the soft x-ray regime, it is especially well suited for the study of 3d-metals and light elements such as nitrogen. Recent developments in vacuum-compatible liquid flat jets have facilitated soft x-ray transmission spectroscopy on molecules in solution, providing information on valence charge distributions of heteroatoms and metal centers. Here, we demonstrate XANES spectroscopy of molecules in solution at the nitrogen K-edge, performed at FLASH, the Free-Electron Laser (FEL) in Hamburg. A split-beam referencing scheme optimally characterizes the strong shot-to-shot fluctuations intrinsic to the process of self-amplified spontaneous emission on which most FELs are based. Due to this normalization, a sensitivity of 1% relative transmission change is achieved, limited by fundamental photon shot noise. The effective FEL bandwidth is increased by streaking the electron energy over the FEL pulse train to measure a wider spectral window without changing FEL parameters. We propose modifications to the experimental setup with the potential of improving the instrument sensitivity by two orders of magnitude, thereby exploiting the high peak fluence of FELs to enable unprecedented sensitivity for femtosecond XANES spectroscopy on liquids in the soft x-ray spectral region.

An evaluation of the cone-shaped pickup performance as a part of the high bandwidth bunch arrival-time monitors (BAMs) for a low charge sub-10 fs arrival-time measurements is presented. Three sets of pickups are installed at the free electron laser FLASH at Deutsches Elektronen-Synchrotron, the quasi-cw SRF accelerator ELBE at the Helmholtz-Zentrum Dresden-Rossendorf and the SwissFEL injector test facility at Paul Scherrer Institute. Measurements and simulations are in good agreement and the pickups fulfill the design specifications. Utilizing the high bandwidth BAM with the cone-shaped pickups, an improvement of the signal slope by a factor of 10 is demonstrated at ELBE compared to the BAM with a low bandwidth.

Wave packet interferometry provides benchmark information on light-induced electronic quantum states by monitoring their relative amplitudes and phases during coherent excitation, propagation, and decay. The relative phase control of soft x-ray pulse replicas on the single-digit attosecond timescale achieved in our experiments makes this method a powerful tool to probe ultrafast quantum phenomena such as the excitation of Auger shake-up states with sub-cycle precision. In this contribution we present first results obtained for different Auger decay channels upon generating L-shell vacancies in argon atoms using Michelson-type all-reflective interferometric autocorrelation at a central free-electron laser photon energy of 274.7 eV.