We present studies of high-order harmonic generation (HHG) in laser ablation plumes of the ribonucleic acid nucleobase uracil and its deoxyribonucleic acid counterpart thymine. Harmonics were generated using 780 nm, 30 fs and 1300 nm, 40 fs radiation upon ablation with 1064 nm, 10 ns or 780 nm, 160 ps pulses. Strong HHG signals were observed from uracil plumes with harmonics emitted with photon energies >55 eV. Results obtained in uracil plumes were compared with those from thymine, which did not yield signs of harmonic generation. The ablation plumes of the two compounds were examined by collection of the ablation debris on a silicon substrate placed in close proximity to the target and by time-of-flight mass spectrometry. From this evidence we conclude that the differences in HHG signal are due to the different fragmentation dynamics of the molecules in the plasma plume. These studies constitute the first attempt to analyse differences in structural properties of complex molecules through plasma ablation-induced HHG spectroscopy.

Ultrashort optical pulses can trigger a variety of non-equilibrium processes in magnetic thin films affecting electrons and spins on femtosecond timescales. In order to probe the charge and magnetic degrees of freedom simultaneously, we developed an X-ray streaking technique that has the advantage of providing a jitter-free picture of absorption cross-section changes. In this paper, we present an experiment based on this approach, which we performed using five photon probing energies at the Ni M2,3-edges. This allowed us to retrieve the absorption and magnetic circular dichroism time traces, yielding detailed information on transient modifications of electron and spin populations close to the Fermi level. Our findings suggest that the observed absorption and magnetic circular dichroism dynamics both depend on the extreme ultraviolet (XUV) probing wavelength, and can be described, at least qualitatively, by assuming ultrafast energy shifts of the electronic and magnetic elemental absorption resonances, as reported in recent work. However, our analysis also hints at more complex changes, highlighting the need for further experimental and theoretical studies in order to gain a thorough understanding of the interplay of electronic and spin degrees of freedom in optically excited magnetic thin films.

High-order harmonic generation in graphite-ablated plasmas was systematically studied using ultrashort (3.5 and 30 fs) laser pulses. We observed the efficient frequency conversion of 3.5 fs Ti:sapphire laser pulses in the range of 15–26 eV. Stabilization of the harmonic yield at a 1 kHz pulse repetition rate was accomplished using a rotating graphite target. We also show the results of harmonic generation in carbon plasma using 1300 nm, 40 ps pulses, which allowed the extension of the harmonic cutoff while maintaining a comparable conversion efficiency to the case of 780 nm driving radiation. The time-of-flight mass spectrometric analysis of the plasma components and the scanning electron microscopy of plasma debris under optimal conditions for harmonic generation suggest the presence of small carbon clusters (C10–C30) in the plasma plume at the moment of femtosecond pulse propagation, which further aggregate on nearby substrates. We present the results of plasma spectroscopy obtained under unoptimized plasma conditions that elucidate the reduction in harmonic signal. We also present calculations of plasma concentration under different excitation conditions of the ablated graphite target.

Enhanced single harmonic generation is analyzed in indium laser ablation plasmas at excitation conditions of multicycle (30 fs) and few-cycle (3.5 fs) pulses. We demonstrate the strong influence of pulse duration, on the emission spectra from the indium plasma. For few-cycle pulses, the enhanced emissions do not coincide with the expected harmonic wavelengths, which is the case for multicycle pulses. We test the coherent properties of an enhanced emission around 20 eV using polarization and double-slit interference techniques. We also characterize the dynamics of the emissions from the indium plasma by tuning the laser pulse duration. A theoretical analysis is presented to describe the indium plasma emission upon excitation by few-cycle pulses.

The use of structured ultrashort pulses with coupled spatiotemporal properties is emerging as a key tool for ultrafast manipulation. Ultrafast vector beams are opening exciting opportunities in different fields such as microscopy, time-resolved imaging, nonlinear optics, particle acceleration or attosecond science. Here, we implement a technique for the full characterization of structured time-dependent polarization light waveforms with spatiotemporal resolution, using a compact twofold spectral interferometer, based on in-line bulk interferometry and fibre-optic coupler assisted interferometry. We measure structured infrared femtosecond vector beams, including radially polarized beams and complex-shaped beams exhibiting both temporal and spatial evolving polarization. Our measurements confirm that light waveforms with polarization evolving at the micrometer and femtosecond scales can be achieved through the use of structured waveplates and polarization gates. This new scale of measurement achieved will open the way to predict, check and optimize applications of structured vector beams at the femtosecond and micrometer scales.

We report on high-order-harmonic generation in nanoparticle-containing laser ablation plasmas using a Ti:sapphire driving laser at a repetition rate of 1 kHz and on the relation of the harmonic signals with the morphological and spectroscopic characteristics of the ablation deposits. The study of the deposits has allowed the definition of ablation conditions, leading to the generation of a plasma containing nanoparticles of similar sizes to the ones used as target material. The corresponding plasma plumes lead to efficient conversion of the IR photons towards the short-wavelength range through high-order harmonic generation and show superior performance to those corresponding to bulk targets of the same metallic element.

Spatially and temporally resolved optical emission spectroscopy has been used to study plasmas formed by 1064 nm pulsed laser ablation of silver targets in a vacuum.

Ultrafast phenomena on a femtosecond timescale are commonly examined by pump-probe experiments. This implies multiple measurements, where the sample under investigation is pumped with a short light pulse and then probed with a second pulse at various time delays to follow its dynamics. Recently, the principle of streaking extreme ultraviolet (XUV) pulses in the temporal domain has enabled recording the dynamics of a system within a single pulse. However, separate pump-probe experiments at different absorption edges still lack a unified timing, when comparing the dynamics in complex systems. Here, we report on an experiment using a dedicated optical element and the two-color emission of the FERMI XUV free-electron laser to follow the charge and spin dynamics in composite materials at two distinct absorption edges, simultaneously. The sample, consisting of ferromagnetic Fe and Ni layers, separated by a Cu layer, is pumped by an infrared laser and probed by a two-color XUV pulse with photon energies tuned to the M-shell resonances of these two transition metals. The experimental geometry intrinsically avoids any timing uncertainty between the two elements and unambiguously reveals an approximately 100 fs delay of the magnetic response with respect to the electronic excitation for both Fe and Ni. This delay shows that the electronic and spin degrees of freedom are decoupled during the demagnetization process. We furthermore observe that the electronic dynamics of Ni and Fe show pronounced differences when probed at their resonance, while the demagnetization dynamics are similar. These observations underline the importance of simultaneous investigation of the temporal response of both charge and spin in multi-component materials. In a more general scenario, the experimental approach can be extended to continuous energy ranges, promising the development of jitter-free transient absorption spectroscopy in the XUV and soft X-ray regimes.