4.6 Article

Angular dependence of the strong-field ionization measured in randomly oriented hydrogen molecules

Journal

PHYSICAL REVIEW A
Volume 79, Issue 3, Pages -

Publisher

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevA.79.033408

Keywords

deuterium; hydrogen neutral molecules; molecular orientation; molecule-photon collisions; photodissociation; photoionisation

Funding

  1. Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy
  2. NSF

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We employed electron-ion coincidence momentum spectroscopy to measure the relative angle between an emitted electron and a deuteron resulting from field dissociation of the molecular ion produced by a circularly polarized pulse. We deduced the angular dependence of the molecular ionization probability without having to align the molecules first. We determined that with 50 fs pulses of 1850 nm wavelength and 2x10(14) W/cm(2) intensity neutral D-2 molecules are 1.15 times more likely to be ionized when the laser electric field is parallel to the molecular axis than for the perpendicular orientation, in excellent agreement with our ab initio theoretical model. Our results also agree with predictions of the molecular Ammosov-Delone-Krainov (mo-ADK) theory, as well as those of a similar experiment performed with 800 nm pulses of comparable intensity and duration on H-2 molecules.

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