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Nature

Getting excited about helium

Randall G. Hulet

Published May 1, 2001• 1 citation
Publisher
DOI
10.1038/35078170

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Investigation of Population Inversion in Helium

W. J. Condell, O. VanGunten, HS Bennett

Get PDF Email Share Share with Facebook Tweet This Post on reddit Share with LinkedIn Add to CiteULike Add to Mendeley Add to BibSonomy Get Citation Copy Citation Text W. J. Condell, O. VanGunten, and H. S. Bennett, "Investigation of Population Inversion in Helium," J. Opt. Soc. Am. 50, 184_1-185 (1960) Export Citation BibTex Endnote (RIS) HTML Plain Text Citation alert Save article

Journal of the Optical Society of America•Feb 1, 1960•1 citation
We report the results of numerical modeling of the coherent action of a single short laser pulse on a multilevel quantum system of metastable and short-lived states of antiprotonic helium. Increasing the pulse intensity we observed more new states getting involved into the coherent interaction, their populations being affected by the pulse. Examples of intensity-dependent dynamics of the metastable states populations are considered. Extraction of spectroscopic information about the states of antiprotonic helium from the experiments with fixed-frequency variable-intensity laser pulses is discussed.
Abstract Ionization of laser-dressed atomic helium is investigated with focus on photoelectron angular distributions stemming from two-color multi-photon excited states. The experiment combines extreme ultraviolet (XUV) with infrared (IR) radiation, while the relative polarization and the temporal delay between the pulses can be varied. By means of an XUV photon energy scan over several electronvolts, we get access to excited states in the dressed atom exhibiting various binding energies, angular momenta, and magnetic quantum numbers. Furthermore, varying the relative polarization is employed as a handle to switch on and off the population of certain states that are only accessible by two-photon excitation. In this way, photoemission can be suppressed for specific XUV photon energies. Additionally, we investigate the dependence of the photoelectron angular distributions on the IR laser intensity. At our higher IR intensities, we start leaving the simple multi-photon ionization regime. The interpretation of the experimental results is supported by numerically solving the time-dependent Schrödinger equation in a single-active-electron approximation. Graphic abstract