The generation of ever shorter pulses is a key to exploring the dynamic behavior of matter on ever shorter time scales. Over the past decade novel ultrafast optical technologies have pushed the duration of laser pulses close to its natural limit, to the wave cycle, which lasts about one femtosecond (1 fs = 10{sup}-15 s) in the visible spectral range. Time-resolved measurements with these pulses are able to trace atomic motion in molecules and related chemical processes. However, electronic dynamics inside atoms often evolve on an attosecond (1 as = 10{sup}-18 s) timescale and require sub-femtosecond pulses for capturing them. This talk will review the recent generation, measurement and first applications of sub-femtosecond soft-X-ray pulses (near 100 eV). These X-ray pulses together with the few-cycle laser pulses used for their generation have opened the way to the development of a technique for attosecond sampling of electrons ejected from atoms. This is accomplished by probing electron emission with the oscillating electric field of the few-cycle laser pulse following an excitation of the atom by the synchronized sub-femtosecond X-ray pulse. Sampling the emission of photo electrons in this manner - with an apparatus that may be regarded as an optical-field-driven "streak camera" - allows time-resolved measurement of the X-ray pulse duration as well as of the laser field oscillations (fig. 1). Tracking the evolution of secondary (Auger) electron emission in addition to that of the primary (photo) electrons with the same system provides time-domain access to inner-shell atomic electron dynamics.
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