Second-order autocorrelation of XUV FEL pulses via time resolved two-photon single ionization of He.

Second-order autocorrelation spectra of XUV free-electron laser pulses from the Spring-8 Compact SASE Source (SCSS) have been recorded by time and momentum resolved detection of two-photon single ionization of He at 20.45 eV using a split-mirror delay-stage in combination with high-resolution recoil-ion momentum spectroscopy (COLTRIMS). From the autocorrelation trace we extract a coherence time of 8 ± 2 fs and a mean pulse duration of 28 ± 5 fs, much shorter than estimations based on electron bunch-length measurements. Simulations within the partial coherence model [Opt. Lett. 35, 3441 (2010)] are in agreement with experiment if a pulse-front tilt across the FEL beam diameter is taken into account that leads to a temporal shift of about 6 fs between both pulse replicas.

Ultrafast extreme ultraviolet induced isomerization of acetylene cations.

Ultrafast isomerization of acetylene cations ([HC=CH](+)) in the low-lying excited A(2)Σ(g)(+) state, populated by the absorption of extreme ultraviolet (XUV) photons (38 eV), has been observed at the Free Electron Laser in Hamburg, (FLASH). Recording coincident fragments C(+) + CH2(+) as a function of time between XUV-pump and -probe pulses, generated by a split-mirror device, we find an isomerization time of 52±15 fs in a kinetic energy release (KER) window of 5.8

Attosecond control of electron dynamics in carbon monoxide.

Laser pulses with stable electric field waveforms establish the opportunity to achieve coherent control on attosecond time scales. We present experimental and theoretical results on the steering of electronic motion in a multielectron system. A very high degree of light-waveform control over the directional emission of C(+) and O(+) fragments from the dissociative ionization of CO was observed. Ab initio based model calculations reveal contributions to the control related to the ionization and laser-induced population transfer between excited electronic states of CO(+) during dissociation.

Three-dimensional momentum imaging of electron wave packet interference in few-cycle laser pulses.

Using a reaction microscope, three-dimensional (3D) electron (and ion) momentum (P) spectra have been recorded for carrier-envelope-phase (CEP) stabilized few-cycle ( approximately 5 fs), intense ( approximately 4 x 10(14) W/cm2) laser pulses (740 nm) impinging on He. Preferential emission of low-energy electrons (E(e)<15 eV) to either hemisphere is observed as a function of the CEP. Clear interference patterns emerge in P space at CEPs with maximum asymmetry, interpreted as attosecond interferences of rescattered and directly emitted electron wave packets by means of a simple model.