Magnetic dichroism in the few-photon ionization of un-polarized and polarized lithium atoms
POSTER
Abstract
In the last decade, the interaction of atoms with circular and elliptically polarized light has been studied extensively. For tunnel-ionization in intense and CEP stabilized laser pulses, it was found that the electron angular distribution exhibits an angular shift. This shift was interpreted to be caused by the finite tunneling time of the active electron that translates into a shift of the mean emission angle due to an angular streaking mechanism often referred to as ‘attoclock’. Here, we report on an experiment where the angular distribution in the two- and three-photon ionization of lithium is investigated. The lithium target can be prepared un-polarized in the 2s ground state or polarized in the 2p (m$_l$=+1) state. A shift in the photo-electron angular distributions is observed that remains even for a fully linearly polarized light if the target atoms are initially excited with a polarization direction perpendicular to ionizing electric field. The observed angular shift is a magnetic dichroism that can interpreted in terms of non-vanishing phase angles between contributing partial waves with different orbital angular momentum. The resemblances and differences of the presently observed angular shift and the attoclock mechanism will be discussed.
Authors
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Santwana Dubey
Missouri University of Science and Technology, Missouri S&T
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Bishnu Acharya
Missouri University of Science and Technology, Missouri S&T
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Kevin Romans
Missouri University of Science and Technology, Missouri S&T
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Nish de Silva
Missouri University of Science and Technology, Missouri S&T
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Katrina Compton
Missouri University of Science and Technology, Missouri S&T
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Kyle Foster
Missouri University of Science and Technology, Missouri S&T
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Cole Rischbieter
Missouri University of Science and Technology, Missouri S&T
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Onyx Russ
Missouri University of Science and Technology, Missouri S&T
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Daniel Fischer
Missouri University of Science and Technology, Missouri S&T