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arXiv:2204.07812 · Physical Review A

Two-path interference in resonance-enhanced few-photon ionization of Li atoms

B. P. Acharya, Santwana Dubey, K. L. Romans, A. H. N. C. De Silva, K. Foster, O. Russ, Klaus Bartschat, Nicolas Douguet, D. Fischer

Published Aug 19, 2022• 9 citations
arXivHTMLPDF

Abstract

We investigate the resonance-enhanced few-photon ionization of atomic lithium by linearly polarized light whose frequency is tuned near the $2s\text{\ensuremath{-}}2p$ transition. Considering the direction of light polarization orthogonal to the quantization axis, the process can be viewed as an atomic ``double-slit experiment'' where the $2p$ states with magnetic quantum numbers ${m}_{\ensuremath{\ell}}=\ifmmode\pm\else\textpm\fi{}1$ act as the slits. In our experiment, we can virtually close one of the two slits by preparing lithium in one of the two circularly polarized $2p$ states before subjecting it to the ionizing radiation. This allows us to extract the interference term between the two pathways and obtain complex phase information on the final state. The experimental results show very good agreement with numerical solutions of the time-dependent Schr\"odinger equation. The validity of the two-slit model is also analyzed theoretically using a time-dependent perturbative approach.

DOI
10.1103/physreva.106.023113

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We investigate few-photon ionization of lithium atoms prepared in the polarized $2p\phantom{\rule{0.16em}{0ex}}({m}_{\ensuremath{\ell}}=+1)$ state when subjected to femtosecond light pulses with left- or right-handed circular polarization at wavelengths between 665 and 920 nm. We consider whether ionization proceeds more favorably for the electric field co- or counter-rotating with the initial electronic current density. Strong asymmetries are found and quantitatively analyzed in terms of ``circular dichroism'' (CD). While the intensity dependence of the measured CD values is rather weak throughout the investigated regime, a very strong sensitivity on the center wavelength of the incoming radiation is observed. While the co-rotating situation overall prevails, the counter-rotating geometry is strongly favored around 800 nm due to the $2p\text{\ensuremath{-}}3s$ resonant transition, which can only be driven by counter-rotating fields. The observed features provide insights into the helicity dependence of light-atom interactions, and on the possible control of electron emission in atomic few-photon ionization by polarization-selective resonance enhancement.
Abstract An all-optical, near-resonant laser atom trap is used to prepare an electronically excited and polarized gas target at mK-temperature for complete photo-ionization studies. As a proof-of-principal experiment, lithium atoms in the 2 2 P 3/2 ( m l = +1) state are ionized by a 266 nm laser source, and emitted electrons and Li + ions are momentum analyzed in a COLTRIMS spectrometer. The excellent resolution achieved in the present experiment allows not only to extract the relative phase and amplitude of all partial waves contributing to the final state, it also enables to characterize the experiment regarding target and spectrometer properties. Photo-electron angular distributions are measured for five different laser polarizations and described in a one-electron approximation with excellent agreement.
A single-atom "double-slit" experiment is realized by photoionizing rubidium atoms using two independent low power lasers. The photoelectron wave of well-defined energy recedes to the continuum either from the 5P or 6P states in the same atom, resulting in two-path interference imaged in the far field using a photoelectron detector. Even though the lasers are independent and not phase locked, the transitions within the atom impart the phase relationship necessary for interference. The experiment is designed so that either 5P or 6P states are excited by one laser, before ionization by the second beam. The measurement cannot determine which excitation path is taken, resulting in interference in wave-vector space analogous to Young's double-slit studies. As the lasers are tunable in both frequency and intensity, the individual excitation-ionization pathways can be varied, allowing dynamic control of the interference term. Since the electron wave recedes in the Coulomb potential of the residual ion, a quantum model is used to capture the dynamics. Excellent agreement is found between theory and experiment.
Abstract We study the three-photon ionization of atomic lithium by intense, short light pulses, via numerically solving the time-dependent Schrödinger equation. Two-photon Rabi oscillations are induced between the 2s and 4s states, which are damped due to single-photon ionization to the p continuum. Developing a minimal three-level model, we analyze the spectral features of the Autler–Townes (AT) doublet that is formed upon the resonant coupling with the laser pulse. Furthermore, we show that this 2 s →→ 4 s → p c o n t i n u u m pathway is the dominant process, if the duration of the laser pulse exceeds a certain value. For shorter pulses, ionization through the 2p state ( 2 s → 2 p → 4 d → f c o n t i n u u m ) gradually becomes the dominant process, provided that the pulse is strong enough to induce several Rabi floppings. Here, we trace the competition of these ionization pathways by observing the structural changes in the shape of the AT doublet.