Intense radiation from lasers has opened up many new areas of research in physics and chemistry, and has revolutionized optical technology. So far, most work in the field of nonlinear processes has been restricted to infrared, visible and ultraviolet light, although progress in the development of X-ray lasers has been made recently. With the advent of a free-electron laser in the soft-X-ray regime below 100 nm wavelength, a new light source is now available for experiments with intense, short-wavelength radiation that could be used to obtain deeper insights into the structure of matter. Other free-electron sources with even shorter wavelengths are planned for the future. Here we present initial results from a study of the interaction of soft X-ray radiation, generated by a free-electron laser, with Xe atoms and clusters. We find that, whereas Xe atoms become only singly ionized by the absorption of single photons, absorption in clusters is strongly enhanced. On average, each atom in large clusters absorbs up to 400 eV, corresponding to 30 photons. We suggest that the clusters are heated up and electrons are emitted after acquiring sufficient energy. The clusters finally disintegrate completely by Coulomb explosion.

The interaction of intense vacuum-ultraviolet radiation from a free-electron laser with rare gas atoms is investigated. The ionization products of xenon and argon atomic beams are analyzed with time-of-flight mass spectroscopy. At 98 nm wavelength and approximately 10(13) W/cm(2) multiple charged ions up to Xe6+ (Ar4+) are detected. From the intensity dependence of multiple charged ion yields the mechanisms of multiphoton processes were derived. In the range of approximately 10(12)-10(13) W/cm(2) the ionization is attributed to sequential multiphoton processes. The production of multiple charged ions saturates at 5-30 times lower power densities than at 193 and 564 nm wavelength, respectively.

The ionization dynamics of Ar and Xe clusters irradiated with intense vacuum ultraviolet light from a free-electron laser is investigated using photoelectron spectroscopy. Clusters comprising between 70 and 900 atoms were irradiated with femtosecond pulses at 95 nm wavelength (approximately 13 eV photon energy) and a peak intensity of approximately 4 x 10(12) W/cm2. A broad thermal distribution of emitted electrons from clusters with a maximum kinetic energy up to 30-40 eV is observed. The observation of relatively low-energy photoelectrons is in good agreement with calculations using a time-dependent Thomas-Fermi model and gives experimental evidence of an outer ionization process of the clusters, due to delayed thermoelectronic emission.

The response of Ar clusters to intense vacuum-ultraviolet pulses is investigated with photoion spec-troscopy. By varying the laser wavelength, the initial excitation was either tuned to absorption bands of surface or bulk atoms of clusters. Multiple ionization is observed, which leads to Coulomb explosion. The efficiency of resonant 2-photon ionization for initial bulk and surface excitation is compared with that of the nonresonant process at different laser intensities. The specific electronic structure of clusters plays almost no role in the explosion dynamics at a peak intensity larger than 1.8 x 10(12) W/cm(2). The inner ionization of atoms for resonant and nonresonant excitation is then saturated and the energy deposition is mainly controlled by the plasma heating rate. Molecular dynamics simulations indicate that standard collisional heating cannot fully account for the strong energy absorption.

The interaction of He atoms with intense vacuum-ultraviolet light of a free-electron laser is investigated using time-of-flight mass spectroscopy and photoelectron spectroscopy. The atoms were irradiated with 100 fs pulses at 95 nm wavelength, which corresponds to ϳ13 eV photon energy. The ionization of He atoms is observed at a peak intensity of 10 10 -10 13 W/cm 2 , which is due both to nonlinear multiphoton ionization with the fundamental wavelength and single-photon ionization with third harmonic radiation of the free-electron laser. The observation of two sharp photoelectron peaks in the kinetic energy spectra, that are separated by the photon energy, is in agreement with the numerical solution of the time-dependent Schrödinger equation. The calculation was done using the fully quantized field and a limited but representative set of basis states. The ionization rate dependence on the laser peak intensity indicates that: ͑a͒ The low-energy peak in the photoelectron spectra is mainly due to two-photon absorption of the fundamental, but ͑b͒ the high-energy peak at 15.4 eV is probably due to third harmonic FEL radiation. The theoretically predicted contribution from threephoton absorption of the fundamental is of about the same order of magnitude and could not be separated from the third harmonic background signal. Particularly, the photoelectron spectra and He + time-of-flight data give evidence that the intensity of third harmonic light is high enough to perform single-shot spectroscopy on gas phase samples.