In principle, the temporal beating of superposed high harmonics obtained by focusing a femtosecond laser pulse in a gas jet can produce a train of very short intensity spikes, depending on the relative phases of the harmonics. We present a method to measure such phases through two-photon, two-color photoionization. We found that the harmonics are locked in phase and form a train of 250-attosecond pulses in the time domain. Harmonic generation may be a promising source for attosecond time-resolved measurements.
The double ionization of helium in the strong-field limit has been studied using an electron-ion coincidence technique. The observed double ionization electron energy spectra differ significantly from the single ionization distributions. This gives new support to the rescattering model of double ionization and explicitly reveals the role of backward electron emission following the e-2e ionizing collision.
The absolute timing of the high-harmonic attosecond pulse train with respect to the generating IR pump cycle has been measured for the first time. The attosecond pulses occur 190+/-20 as after each pump field maxima (twice per optical cycle), in agreement with the "short" quantum path of the quasiclassical model of harmonic generation.
We present an alternative method for measuring ultrashort extreme-ultraviolet pulses that can be synchronized with an intense infrared pulse. The method, based on photoionization of a target atom by the extremeultraviolet pulse in the presence of the infrared pulse, has a potential accuracy of close to 1 fs and is susceptible to single-shot operation. It is demonstrated on harmonic 15 of a titanium:sapphire laser. The minimum pulse duration that can be measured is limited only by the frequency of the radiation used for the ponderomotive shift of the ionization potential ͑3 fs in the case of the titanium:sapphire fundamental͒.
We investigate high harmonics generated from rubidium atoms irradiated simultaneously by an intense 3.5 microm fundamental field and a weak cw diode laser. When 5p, 5d, and 4d excited states are populated through cascade excitation or deexcitation, orders-of-magnitude increases in harmonic yield as compared with the ground state are observed. It appears that, quite unexpectedly, the population accumulated in the 4d state alone is responsible for the observed enhancement.
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