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Pulse duration dependence of strong-field-induced fragmentation of ethylene and acetylene molecules

POSTER

Abstract

Understanding the fragmentation of small polyatomic molecules induced by a strong laser field is one of the key steps towards laser-controlled chemistry. For hydrocarbons, such fragmentation dynamics often involve hydrogen migration in different stages of the breakup process. Here we show how the breakup patterns of ethylene and acetylene molecules exposed to intense 800 nm laser fields change as a function of a laser pulse duration. Performing coincident momentum imaging of ionic fragments resulting from two- and three-body breakup of doubly and triply ionized molecules, we trace the signatures of hydrogen migration, analyze the role of different intermediate states, and discuss possible contributions of ``concerted'' and ``sequential'' fragmentation pathways.

Authors

  • Yubaraj Malakar

    J. R. Macdonald Laboratory, Department of Physics, Kansas State University

  • Farzaneh Ziaee

    J.R. Macdonald Laboratory, Department of Physics, Kansas State University, J. R. Macdonald Laboratory, Department of Physics, Kansas State University, Kansas State University

  • Surjendu Bhattacharyya

    Kansas State University, J. R. Macdonald Laboratory, Department of Physics, Kansas State University

  • Keyu Chen

    J. R. Macdonald Laboratory, Department of Physics, Kansas State University, Kansas State University

  • Kurtis Borne

    J. R. Macdonald Laboratory, Department of Physics, Kansas State University, Kansas State University

  • Wright Lee Pearson

    J. R. Macdonald Laboratory, Department of Physics, Kansas State University

  • Daniel Rolles

    Kansas State University, J.R. Macdonald Lab, Kansas State University, J. R. Macdonald Laboratory, Department of Physics, Kansas State University

  • Artem Rudenko

    Kansas State University, J. R. Macdonald Laboratory, Department of Physics, Kansas State University