Nonlinear responses to an optical field are universal in nature but have been difficult to observe in the extreme ultraviolet (XUV) and soft X-ray regions owing to a lack of coherent intense light sources. High harmonic generation is a well-known nonlinear optical phenomenon and is now drawing much attention in attosecond pulse generation. For the application of high harmonics to nonlinear optics in the XUV and soft X-ray regime, optical pulses should have both large pulse energy and short pulse duration to achieve a high optical electric field. Here we show the generation of intense isolated pulses from a single harmonic (photon energy 27.9 eV) by using a sub-10-femtosecond blue laser pulse, producing a large dipole moment at the relatively low (ninth) harmonic order nonadiabatically. The XUV pulses with pulse durations of 950 attoseconds and 1.3 femtoseconds were characterized by an autocorrelation technique, based on two-photon above-threshold ionization of helium atoms. Because of the small cross-section for above-threshold ionization, such an autocorrelation measurement of XUV pulses with photon energy larger than the ionization energy of helium has not hitherto been demonstrated. The technique can be extended to the characterization of higher harmonics at shorter wavelengths.
Time-resolved photoelectron spectroscopy (trPES) can directly detect transient electronic structure, thus bringing out its promising potential to clarify nonequilibrium processes arising in condensed matters. Here we report the result of core-level (CL) trPES on 1T -TaS 2 , realized by developing a high-intensity 60 eV laser obtained by high-order harmonic (HH) generation. Ta4f CL-trPES offers the transient amplitude of the charge-density-wave (CDW), via the site-selective and real-time observation of Ta electrons. The present result indicates an ultrafast photoinduced melting and recovery of CDW amplitude, followed by a peculiar long-life oscillation (i.e. collective amplitudon excitation) accompanying the transfer of 0.01 electrons among adjacent Ta atoms. CLtrPES offers a broad range of opportunities for investigating the ultrafast atom-specific electron dynamics in photo-related phenomena of interest.
We report on the development of an optical parametric chirpedpulse amplifier at a 1-kHz repetition rate with a 5.5-fs pulse duration, a 2.7-mJ pulse energy and carrier-envelope phase-control. The amplifier is pumped by a 450-nm pulse from a frequency-doubled Ti:sapphire laser.
We report the results of our studies on the selection of the quantum path in high-harmonic generation (HHG) with a relative-phase-locked two-color laser field. It is shown that by tuning the relative phase between fundamental and second-harmonic fields, The timing of tunnel ionization and subsequent electron trajectories on the sub-cycle time scale can be controlled. We have clearly observed a phase-dependent two-step feature in the harmonic spectra that can be attributed to the selection of two major trajectories in the two-color field HHG.
We demonstrate an optical parametric chirped-pulse amplification (OPCPA) system with the pulse energy of 1.5 mJ at a 1 kHz repetition rate. The newly developed 100 ps Ti:sapphire pump laser system, which was optically synchronized with OPCPA seed pulses, delivered 10 mJ, 400 nm pump pulses. After three-stage parametric amplification, recompression of the amplifier output from 45 ps to 6.4 fs was performed. The pulse width of 6.4 fs is, to our knowledge, the shortest ever obtained by OPCPA, and the average power of 1.5 W (1.5 mJ, 1 kHz) is believed to be the highest among few-cycle OPCPA systems.
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