Ultrafast Time-Resolved Soft X-Ray Photoelectron Spectroscopy of Dissociating Br2

Lora Nugent-Glandorf, Michael Scheer, David A. Samuels, Anneliese M. Mulhisen, Edward R. Grant, Xueming Yang, Veronica M. Bierbaum, and Stephen R. Leone
Phys. Rev. Lett. 87, 193002 – Published 22 October 2001
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Abstract

The dissociation of excited state Br2 is probed with the novel technique of ultrafast soft x-ray photoelectron spectroscopy. Excited Br2 molecules are prepared in the dissociative Πu1 state with 80 fs, 400 nm pulses, and a series of photoelectron spectra are obtained during dissociation with pulses of soft x-ray light (47 nm, 26.4 eV, 250 fs). The formation of Br atoms is readily detected and the data support an extremely fast dissociation time for Br2 on the order of 40 fs. Amplitudes of the pump-probe features reveal that the ionization cross section of atomic Br at 47 nm is 40 times larger than that of Br2.

  • Received 21 May 2001

DOI:https://doi.org/10.1103/PhysRevLett.87.193002

©2001 American Physical Society

Authors & Affiliations

Lora Nugent-Glandorf, Michael Scheer*, David A. Samuels, Anneliese M. Mulhisen, Edward R. Grant, Xueming Yang, Veronica M. Bierbaum, and Stephen R. Leone§

  • JILA, National Institute of Standards and Technology and Department of Chemistry and Biochemistry, Department of Physics, University of Colorado, Boulder, Colorado 80309-0440

  • *Present address: Nortel Networks, MS 04332F15, Nepean, Ontario, Canada, K2H 8E9.
  • JILA Visiting Fellow. Permanent address: Department of Chemistry, Purdue University, West Lafayette, IN 47907.
  • JILA Visiting Fellow. Permanent address: Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei, Taiwan.
  • §Also Quantum Physics Division, National Institute of Standards and Technology.

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Vol. 87, Iss. 19 — 5 November 2001

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