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Physical Review A

Floquet description of multiphoton processes in Li

D. I. Duncan, J. G. Story, Thomas F. Gallagher

Published Sep 1, 1995• 10 citations
Publisher

Abstract

We have made several different types of measurements of the three-photon ionization of Li produced by 3-ps laser pulses and describe the results using a Floquet picture. Over the photon frequency range 15 000 to 15 800 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$, Li represents a strongly coupled three-state system with the 2s ground state coupled to the 2p and 3d states by one and two photons, respectively. Energy analysis of the photoelectrons allows the measurement of the intensity dependent shift of the 2s Floquet state during the laser pulse. The shift shows a strong frequency dependence that is not predicted by first-order perturbation theory. We have also measured the total ionization spectrum over several ranges of frequency, as well as the angular distribution of the ionization and the first above-threshold ionization peak for frequencies where the ground state is near resonance with the 4s and 4d excited states. Calculations based on the Floquet Hamiltonian indicate that all of these processes may be understood in terms of a Floquet description.

DOI
10.1103/physreva.52.2209

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We have made several different types of measurements of the three-photon ionization of Li produced by 3-ps laser pulses and describe the results using a Floquet picture. Over the photon frequency range 15 000 to 15 800 cm\ensuremath−1{\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}cm\ensuremath−1, Li represents a strongly coupled three-state system with the 2s ground state coupled to the 2p and 3d states by one and two photons, respectively. Energy analysis of the photoelectrons allows the measurement of the intensity dependent shift of the 2s Floquet state during the laser pulse. The shift shows a strong frequency dependence that is not predicted by first-order perturbation theory. We have also measured the total ionization spectrum over several ranges of frequency, as well as the angular distribution of the ionization and the first above-threshold ionization peak for frequencies where the ground state is near resonance with the 4s and 4d excited states. Calculations based on the Floquet Hamiltonian indicate that all of these processes may be understood in terms of a Floquet description.
We have measured the three photon ionization and electron energy spectra of Na from 5-ps laser pulses over the range 16 300 to 17 800 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$. Together these measurements suggest that multiphoton ionization can be understood in terms of a Floquet description. Sharp discontinuities in the ionization probability and Rabi splittings in the electron energy spectra are direct consequences of adiabatic and diabatic evolution, respectively, from the initial zero-field ground state.
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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.
When exposed to intense light of \ensuremath{\sim}580 nm, the ground state of K shifts up in energy, passing through two-photon resonances with Rydberg states and finally crossing the two-photon ionization limit. Using laser pulses of 0.5 to 13 ps duration, we have shown experimentally that ionization occurs for short pulses, but for long pulses the population is diverted into the Rydberg states where some population survives the peak intensity of the pulse, in excellent agreement with a dynamic Floquet model.
A joint experimental and theoretical study of four-photon ionization of Li is performed using a pump-probe setup with the laser frequency tuned in between the excitation energies of the 2s2s2s--4p4p4p and 2s2s2s--4f4f4f three-photon transitions. The three-dimensional photoelectron momentum pattern is recorded as a function of the delay time between two otherwise identical laser pulses. The process is modeled by numerically solving the time-dependent Schr\"odinger equation. While complicated interference patterns arise in the electron spectrum when the two pulses partially overlap in time, the expected quantum-beat phenomenon between Li atoms in either the 4p4p4p or the 4f4f4f state are seen when the fast oscillations involving the 2s2s2s initial state are averaged over. The qualitative agreement between the predicted and observed beating patterns is very good.
It has been widely believed that short-pulse multiphoton ionization is dominated by a resonance process: excited states of the atom are shifted by the radiation field into multiphoton resonance with the ground state, are populated, and then rapidly ionized. A recent experiment, shows significant population remaining in excited states at the end of the laser pulse, and this result has been interpreted as indicating that ionization proceeds slowly out of these states. We investigate this issue in the framework of Floquet theory, supplemented by direct numerical solution of the time-dependent Schrodinger equation. In this framework, the standard picture is portrayed as an adiabatic transition between Floquet eigenstates, which occurs as the amplitude of the laser field is ramped through the resonance value (i.e. through an avoided crossing of Floquet quasienergies). Thus it follows that the same type of transition must occur as the field is turned off. This mechanism can yield significant populations of excited states that do not suffer appreciable ionization. We exhibit this effect by numerical studies of a model atom with two bound states and two continua.