Article

Nature 414, 509-513 (29 November 2001) | doi:10.1038/35107000; Received 1 October 2001; Accepted 19 October 2001

Attosecond metrology

M. Hentschel1,2, R. Kienberger1,2, Ch. Spielmann1, G. A. Reider1, N. Milosevic1, T. Brabec1, P. Corkum3, U. Heinzmann4, M. Drescher4 and F. Krausz1

  1. Institut für Photonik, Technische Universität Wien, Gusshausstr. 27, A-1040 Wien, Austria
  2. Steacie Institute of Molecular Sciences, NRC Canada, Ottawa, Canada K1A 0R6
  3. Fakultät für Physik, Universität Bielefeld, D-33615 Bielefeld, Germany
  4. These authors contributed equally to this work

Correspondence to: F. Krausz1 Correspondence and requests for materials should be addressed to F.K. (e-mail: Email: ferenc.krausz@tuwien.ac.at).

The generation of ultrashort pulses is a key to exploring the dynamic behaviour of matter on ever-shorter timescales. Recent developments have pushed the duration of laser pulses close to its natural limit—the wave cycle, which lasts somewhat longer than one femtosecond (1 fs = 10-15 s) in the visible spectral range. Time-resolved measurements with these pulses are able to trace dynamics of molecular structure, but fail to capture electronic processes occurring on an attosecond (1 as = 10-18 s) timescale. Here we trace electronic dynamics with a time resolution of less than or equal to 150 as by using a subfemtosecond soft-X-ray pulse and a few-cycle visible light pulse. Our measurement indicates an attosecond response of the atomic system, a soft-X-ray pulse duration of 650 plusminus 150 as and an attosecond synchronism of the soft-X-ray pulse with the light field. The demonstrated experimental tools and techniques open the door to attosecond spectroscopy of bound electrons.

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