Attosecond metrology has so far largely remained limited to titanium:sapphire lasers combined with an active stabilization of the carrier-envelope phase (CEP). These sources limit the achievable photon energy to ∼100 eV which is too low to access X-ray absorption edges of most second- and third-row elements which are central to chemistry, biology and material science. Therefore, intense efforts are underway to extend attosecond metrology to the soft-X-ray (SXR) domain using mid-infrared (mid-IR) drivers. Here, we introduce and experimentally demonstrate a method that solves the long-standing problem of the complete temporal characterization of ultra-broadband (≫10 eV) attosecond pulses. We generalize the recently proposed Volkov-transform generalized projection algorithm (VTGPA) to the case of multiple overlapping photoelectron spectra and demonstrate its application to isolated attosecond pulses. This new approach overcomes all key limitations of previous attosecond-pulse reconstruction methods, in particular the central-momentum approximation (CMA), and it incorporates the physical, complex-valued and energy-dependent photoionization matrix elements. These properties make our approach general and particularly suitable for attosecond supercontinua of arbitrary bandwidth. We apply this method to attosecond SXR pulses generated from a two-cycle mid-IR driver, covering a bandwidth of ∼100 eV and reaching photon energies up to 180 eV. We extract an SXR pulse duration of (43±1) as from our streaking measurements, defining a new world record. Our results prove that the popular and broadly available scheme of post-compressing the output of white-light-seeded optical parametric amplifiers is adequate to produce high-contrast isolated attosecond pulses covering the L-edges of silicon, phosphorous and sulfur. Our new reconstruction method and experimental results open the path to the production and characterization of attosecond pulses lasting less than one atomic unit of time (24 as) and covering X-ray absorption edges of most light elements.

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High–harmonic generation (HHG) in gases has been the main enabling technology of attosecond science since its discovery. Recently, HHG from solids has been demonstrated, opening a lively area of research. In contrast, harmonic generation from liquids has so far remained restricted to low harmonics in the visible regime. Here, we report the observation and detailed characterization of extreme ultraviolet HHG from liquid water and several alcohols extending beyond 20 eV. This advance was enabled by the implementation of the recent liquid flat–microjet technology, which we show to facilitate the spatial separation of HHG from the bulk liquid and the surrounding gas phase. We observe striking differences between the HHG spectra of water and several alcohols. A comparison with a strongly–driven few–band model establishes the sensitivity of HHG to the electronic structure of liquids. Our results suggest liquid–phase high–harmonic spectroscopy as a new method for studying the electronic structure and ultrafast scattering processes in liquids.

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We demonstrate intense high-order harmonic generation from plasma that is created from different carbon targets. We obtain high-order harmonic energy in the multi-microjoule range for each harmonic order from the 11th to the 17th harmonic. By analyzing the target morphology and the plasma composition, we conclude that the intense harmonics from the bulk carbon targets originate from nanoparticles target.