Direct mapping of curve-crossing dynamics in IBr by attosecond transient absorption spectroscopy

Author:

Kobayashi Yuki1ORCID,Chang Kristina F.1ORCID,Zeng Tao2ORCID,Neumark Daniel M.13ORCID,Leone Stephen R.134ORCID

Affiliation:

1. Department of Chemistry, University of California, Berkeley, CA 94720, USA.

2. Department of Chemistry, Carleton University, Ottawa, Ontario K1S5B6, Canada.

3. Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

4. Department of Physics, University of California, Berkeley, CA 94720, USA.

Abstract

A panoramic view of photodissociation As light pulses get shorter in time, they correspondingly get broader in frequency. Kobayashi et al. take advantage of both properties of attosecond pulses to elucidate iodine monobromide (IBr) photodissociation by detecting ultrafast bromine and iodine spectral shifts simultaneously. A preliminary burst of light weakens the I–Br bond. Then, as the atoms fly apart, they reach a configuration where the bond vibration can couple ground and excited electronic states. The broadband probe pulse reveals rapid changes in each atom's electronic structure at this juncture. Science , this issue p. 79

Funder

National Science Foundation

National Institutes of Health

Army Research Office

Carleton University

Natural Sciences and Engineering Research Council of Canada

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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