An era of exploring the interactions of high-intensity, hard X-rays with matter has begun with the start-up of a hard-X-ray free-electron laser, the Linac Coherent Light Source (LCLS). Understanding how electrons in matter respond to ultra-intense X-ray radiation is essential for all applications. Here we reveal the nature of the electronic response in a free atom to unprecedented high-intensity, short-wavelength, high-fluence radiation (respectively 10(18) W cm(-2), 1.5-0.6 nm, approximately 10(5) X-ray photons per A(2)). At this fluence, the neon target inevitably changes during the course of a single femtosecond-duration X-ray pulse-by sequentially ejecting electrons-to produce fully-stripped neon through absorption of six photons. Rapid photoejection of inner-shell electrons produces 'hollow' atoms and an intensity-induced X-ray transparency. Such transparency, due to the presence of inner-shell vacancies, can be induced in all atomic, molecular and condensed matter systems at high intensity. Quantitative comparison with theory allows us to extract LCLS fluence and pulse duration. Our successful modelling of X-ray/atom interactions using a straightforward rate equation approach augurs favourably for extension to complex systems.

In 1964 Keldysh1 helped lay the foundations of strong-field physics by introducing a theoretical framework that characterized atomic ionization as a process that evolves with the intensity and wavelength of the fundamental field. Within this context, experiments 2 have examined the intensity-dependent ionization but, except for a few cases, technological limitations have confined the majority to wavelengths below 1 µm. The development of intense, ultrafast laser sources in the midinfrared (1 µm < l < 5 µm) region enables exploration of the wavelength scaling of the Keldysh picture while enabling new opportunities in strong-field physics, control of electronic motion and attosecond science. Here we report a systematic experimental investigation of the wavelength scaling in this region by concurrently analysing the production of energetic electrons and photons emitted by argon atoms interacting with few-cycle, mid-infrared fields. The results support the implicit predictions contained in Keldysh's work, and pave the way to the realization of brighter and shorter attosecond pulsed light sources using longer-wavelength driving fields. Keldysh 1 described the two main effects an intense lowfrequency laser field has on an atom as (1) a bending of the Coulomb potential by the field, forming a sufficiently narrow barrier for the electron to tunnel into the continuum, and (2) an oscillating motion of the free electron induced by the field of strength E and frequency ω. The cycle-averaged kinetic energy of the oscillating electron (ponderomotive energy) is given in atomic units as U p = E 2 /4ω 2 . The limit of validity of the Keldysh approach is defined by the condition that the adiabaticity parameter γ = √

No abstract

Elementary processes associated with ionization of liquid water provide a framework for understanding radiation-matter interactions in chemistry and biology. Although numerous studies have been conducted on the dynamics of the hydrated electron, its partner arising from ionization of liquid water, H2O+, remains elusive. We used tunable femtosecond soft x-ray pulses from an x-ray free electron laser to reveal the dynamics of the valence hole created by strong-field ionization and to track the primary proton transfer reaction giving rise to the formation of OH. The isolated resonance associated with the valence hole (H2O+/OH) enabled straightforward detection. Molecular dynamics simulations revealed that the x-ray spectra are sensitive to structural dynamics at the ionization site. We found signatures of hydrated-electron dynamics in the x-ray spectrum.

We have studied the photoinduced low spin (LS) to high spin (HS) conversion of [Fe(bipy)(3)](2+) in aqueous solution. In a laser pump/X-ray probe synchrotron setup permitting simultaneous, time-resolved X-ray diffuse scattering (XDS) and X-ray spectroscopic measurements at a 3.26 MHz repetition rate, we observed the interplay between intramolecular dynamics and the intermolecular caging solvent response with better than 100 ps time resolution. On this time scale, the initial ultrafast spin transition and the associated intramolecular geometric structure changes are long completed, as is the solvent heating due to the initial energy dissipation from the excited HS molecule. Combining information from X-ray emission spectroscopy and scattering, the excitation fraction as well as the temperature and density changes of the solvent can be closely followed on the subnanosecond time scale of the HS lifetime, allowing the detection of an ultrafast change in bulk solvent density. An analysis approach directly utilizing the spectroscopic data in the XDS analysis effectively reduces the number of free parameters, and both combined permit extraction of information about the ultrafast structural dynamics of the caging solvent, in particular, a decrease in the number of water molecules in the first solvation shell is inferred, as predicted by recent theoretical work.

Improving the temporal contrast of ultrashort and ultraintense laser pulses is a major technical issue for high-field experiments. This can be achieved using a so-called "plasma mirror." We present a detailed experimental and theoretical study of the plasma mirror that allows us to quantitatively assess the performances of this system. Our experimental results include time-resolved measurements of the plasma mirror reflectivity, and of the phase distortions it induces on the reflected beam. Using an antireflection coated plate as a target, an improvement of the contrast ratio by more than two orders of magnitude can be achieved with a single plasma mirror. We demonstrate that this system is very robust against changes in the pulse fluence and imperfections of the beam spatial profile, which is essential for applications.

We show that high fluence, high-intensity x-ray pulses from the world's first hard x-ray free-electron laser produce nonlinear phenomena that differ dramatically from the linear x-ray-matter interaction processes that are encountered at synchrotron x-ray sources. We use intense x-ray pulses of sub-10-fs duration to first reveal and subsequently drive the 1s↔2p resonance in singly ionized neon. This photon-driven cycling of an inner-shell electron modifies the Auger decay process, as evidenced by line shape modification. Our work demonstrates the propensity of high-fluence, femtosecond x-ray pulses to alter the target within a single pulse, i.e., to unveil hidden resonances, by cracking open inner shells energetically inaccessible via single-photon absorption, and to consequently trigger damaging electron cascades at unexpectedly low photon energies.

X-ray free-electron lasers (FELs) produce femtosecond x-ray pulses with unprecedented intensities that are uniquely suited for studying many phenomena in atomic, molecular, and optical (AMO) physics. A compilation of the current developments at the Linac Coherent Light Source (LCLS) and future plans for the LCLS-II and Next Generation Light Source (NGLS) are outlined. The AMO instrumentation at LCLS and its performance parameters are summarized. A few selected experiments representing the rapidly developing field of ultra-fast and peak intensity x-ray AMO sciences are discussed. These examples include fundamental aspects of intense x-ray interaction with atoms, nonlinear atomic physics in the x-ray regime, double core-hole spectroscopy, quantum control experiments with FELs and ultra-fast x-ray induced dynamics in clusters. These experiments illustrate the fundamental aspects of the interaction of intense short pulses of x-rays with atoms, molecules and clusters that are probed by electron and ion spectroscopies as well as ultra-fast x-ray scattering.