High-harmonic spectroscopy is an all-optical nonlinear technique with inherent attosecond temporal resolution. It has been applied to a variety of systems in the gas phase and solid state. Here we extend its use to liquid samples. By studying high-harmonic generation over a broad range of wavelengths and intensities, we show that the cut-off energy is independent of the wavelength beyond a threshold intensity and that it is a characteristic property of the studied liquid. We explain these observations with a semi-classical model based on electron trajectories that are limited by the
electron scattering. This is further confirmed by measurements performed with elliptically polarized light and with ab-initio time-dependent density functional theory calculations. Our results propose high-harmonic spectroscopy as an all-optical approach for determining the effective mean free paths of slow electrons in liquids.
Effects of extreme nonlinear optics, such as high harmonic generation (HHG), are conventionally modeled with classical electromagnetic fields: both the driving and emitted fields are treated classically. We present the fully quantum electrodynamical theory of extreme nonlinear optics and use it to predict new quantum effects in HHG. The quantum description shows new effects in both the spectral and statistical properties of HHG. We also describe how the HHG process changes in the single-atom regime and discuss experiments that can test our various predictions. Revealing the quantum-optical nature of HHG could lead to novel sources of attosecond light having intrinsically quantum statistics, such as squeezing and entanglement.
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