We have investigated the intensity dependence of high-order harmonic generation in argon when the two shortest quantum paths contribute to the harmonic emission. For the first time to our knowledge, experimental conditions were found to clearly observe interference between these two quantum paths that are in excellent agreement with theoretical predictions. This result is a first step towards the direct experimental characterization of the full single-atom dipole moment and demonstrates an unprecedented accuracy of quantum path control on an attosecond time scale.
We demonstrate an extremely accurate method for measuring ultrabroadband, sub-10 fs pulses even if they exhibit a highly modulated spectrum, space-time coupling, or both. The method uses a spatially encoded arrangement for spectral phase interferometry for direct electric field reconstruction, which allows a zero additional phase measurement to be performed with a relatively low signal-to-noise ratio in real time and single shot.
We propose a method for the complete characterization of attosecond duration electromagnetic pulses produced by high harmonic generation in an atomic gas. Our method is based on self-referencing spectral interferometry of two spectrally sheared extreme ultraviolet pulses, which is achieved by pumping the harmonic source with two sheared optical driving pulses. The resulting interferogram contains sufficient information to completely reconstruct the temporal behavior of the electric field. We demonstrate that such a method is feasible, and outline two possible experimental configurations.
We present a technique for frequency-resolved wavefront characterization of high harmonics based on lateral shearing interferometry. Tilted replicas of the driving laser pulse are produced by a Mach-Zehnder interferometer, producing separate focii in the target. The interference of the resulting harmonics on a flat-field extreme ultraviolet spectrometer yields the spatial phase derivative. A comprehensive set of spatial profiles, resolved by harmonic order, validate the technique and reveal the interplay of single-atom and macroscopic effects.
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