Probing Electron Dynamics in Simple Molecules with Attosecond Pulses

  • Paula Rivière
  • Alicia Palacios
  • Jhon Fredy Pérez-Torres
  • Fernando Martín
Chapter
Part of the Springer Series in Chemical Physics book series (CHEMICAL, volume 103)

Abstract

Attosecond pulses are an ideal tool to explore electron and nuclear dynamics in atoms and molecules. Either as single attosecond pulses (SAP), in attosecond pulse trains (APT), or in combination with infrared (IR) pulses, these pulses, with frequencies in the VUV-XUV regime, have been widely used to probe ionization, electron tunneling, or autoionization in atoms. More recently, similar processes have been studied in molecules. A correct theoretical description of such processes in molecules often requires a fully dimensional treatment due to the important role of nuclear motion and electron correlation. This restricts ab initio calculations to the simplest molecules. In this chapter, we discuss single ionization of hydrogen molecules (H2 and D2) induced by time-delayed SAP+IR and APT+IR schemes. Ab initio time-dependent theoretical calculations are compared with existing experiments.

Keywords

Ionization Probability Dissociative Ionization Kinetic Energy Distribution Attosecond Pulse Nuclear Dynamic 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2012

Authors and Affiliations

  • Paula Rivière
    • 1
  • Alicia Palacios
    • 1
  • Jhon Fredy Pérez-Torres
    • 1
  • Fernando Martín
    • 1
    • 2
  1. 1.Departamento de Química, Módulo 13Universidad Autónoma de MadridMadridSpain
  2. 2.Instituto Madrileño de Estudios Avanzados en NanocienciaMadridSpain

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