Article

Nature 419, 803-807 (24 October 2002) | doi:10.1038/nature01143; Received 5 August 2002; Accepted 20 September 2002

Time-resolved atomic inner-shell spectroscopy

M. Drescher1,2, M. Hentschel1, R. Kienberger1, M. Uiberacker1, V. Yakovlev1, A. Scrinzi1, Th. Westerwalbesloh2, U. Kleineberg2, U. Heinzmann2 and F. Krausz1

  1. Institut für Photonik, Technische Universität Wien, Gusshausstrasse 27, A-1040 Wien, Austria
  2. Fakultät für Physik, Universität Bielefeld, Universitätsstrasse 25, D-33615 Bielefeld, Germany

Correspondence to: M. Drescher1,2F. Krausz1 Correspondence and requests for materials should be addressed to M.D. (e-mail: Email: drescher@physik.uni-bielefeld.de) or F.K. (e-mail: Email: ferenc.krausz@tuwien.ac.at).

The characteristic time constants of the relaxation dynamics of core-excited atoms have hitherto been inferred from the linewidths of electronic transitions measured by continuous-wave extreme ultraviolet or X-ray spectroscopy. Here we demonstrate that a laser-based sampling system, consisting of a few-femtosecond visible light pulse and a synchronized sub-femtosecond soft X-ray pulse, allows us to trace these dynamics directly in the time domain with attosecond resolution. We have measured a lifetime of 7.9-0.9+1.0 fs of M-shell vacancies of krypton in such a pump–probe experiment.

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