Abstract
Attosecond pulses at photon energies that cover the principal absorption edges of the building blocks of materials are a prerequisite for time-resolved probing of the triggering events leading to electronic dynamics such as exciton formation and annihilation. We demonstrate experimentally the isolation of individual attosecond pulses at the carbon K-shell edge (284 eV) in the soft X-ray water window with pulse duration below 400 as and with a bandwidth supporting a 30-as pulse duration. Our approach is based on spatiotemporal isolation of long-wavelength-driven harmonics and validates a straightforward and scalable approach for robust and reproducible attosecond pulse isolation.
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CITATION STYLE
Silva, F., Teichmann, S. M., Cousin, S. L., Hemmer, M., & Biegert, J. (2015). Spatiotemporal isolation of attosecond soft X-ray pulses in the water window. Nature Communications, 6. https://doi.org/10.1038/ncomms7611
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