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Journal of the Optical Society of America B

Fully relativistic description of the power spectrum

Octavian Postavaru

Published Jul 26, 2018• 4 citations
Publisher

Abstract

Resonance fluorescence of laser-driven atoms is studied in the relativistic regime by solving the time-dependent Dirac equation in a multi-level model. Electron spin and retardation of the electron–photon interaction give rise to new phenomena such as splitting of sideband peaks and modification of the Rabi oscillator frequencies not explainable in a nonrelativistic theory. In our theoretical investigation, we show how, by applying coherent light with x-ray frequencies, the relativistic fluorescence spectrum can be exploited to determine atomic multipole matrix elements.

DOI
10.1364/josab.35.002000

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Resonance fluorescence of laser-driven atoms is studied in the relativistic regime by solving the time-dependent Dirac equation in a multi-level model. Electron spin and retardation of the electron–photon interaction give rise to new phenomena such as splitting of sideband peaks and modification of the Rabi oscillator frequencies not explainable in a nonrelativistic theory. In our theoretical investigation, we show how, by applying coherent light with x-ray frequencies, the relativistic fluorescence spectrum can be exploited to determine atomic multipole matrix elements.
We present the relativistic power spectrum for the interaction of an x-ray field with an highly charged ion, obtained by solving the time-dependent Dirac equation in a two-level approximation [1]. The phenomenon of splitting of sideband peaks is obtained as a consequence of the introduction in theory of the electronic spin. Also this phenomenon together with the retardation of the electron-photon interaction changes the values of Rabi frequencies. After describing the fluorescence spectrum, we show how it can be used to determine atomic multipole matrix elements.
Resonance fluorescence of laser-driven highly charged ions is investigated with regard to precisely measuring atomic properties. For this purpose an ab initio approach based on the Dirac equation is employed that allows for studying relativistic ions. These systems provide a sensitive means to test correlated relativistic dynamics, quantum electrodynamic phenomena and nuclear effects by applying x-ray lasers. We show how the narrowing of sidebands in the x-ray fluorescence spectrum by interference due to an additional optical driving can be exploited to determine atomic dipole or multipole moments to unprecedented accuracy.
The phenomenon of resonance fluorescence provides an interesting manifestation of the quantum theory of light and is a “real world” application of the material of the Chapters 8 and 9. In this process, a two-level atom is typically driven by a resonant continuous-wave laser field and the spectral and quantum statistical properties of the fluorescent light emitted by the atom are measured. Experimentally this can be achieved by scattering a laser off a collimated atomic beam such that the directions of the laser beam, atomic beam, and detector axis are mutually perpendicular as shown in Fig. 10.1. If the driving field is monochromatic, then at low excitation intensity the atom absorbs a photon at the excitation frequency and reemits it at the same frequency as a consequence of conservation of energy. The spectral width of the fluorescent light is therefore very narrow. The situation, however, is considerably more complicated when the excitation intensity increases and the Rabi frequency associated with the driving field becomes comparable to, or larger than, the atomic linewidth. At such intensity levels, the Rabi oscillations show up as a modulation of the quantum dipole moment and sidebands start emerging in the spectrum of the emitted radiation. This so-called dynamic Stark splitting is an interesting feature of the atom–field interaction. In addition to that, the fluorescent light exhibits certain nonclassical properties including photon antibunching and squeezing. In this chapter, we develop a theory of resonance fluorescence to explain these phenomena.
In this thesis we investigate strong-field relativistic processes in highly charged ions. In the first part,we study resonance fluorescence of laser-driven highly charged ions in the relativistic regime by solving the time-dependent master equation in a multi-level model. Our ab initio approach based on the Dirac equation allows for investigating highly relativistic ions, and, consequently, provides a sensitive means to test correlated relativistic dynamics, bound-state quantum electrodynamic phenomena and nuclear effects by applying coherent light with x-ray frequencies. Atomic dipole or multipole moments may be determined to unprecedented accuracy by measuring the interference-narrowed fluorescence spectrum. Furthermore, we investigate the level structure of heavy hydrogenlike ions in laser beams. Interaction with the light field leads to dynamic shifts of the electronic energy levels, which is relevant for spectroscopic experiments. We apply a fully relativistic description of the electronic states by means of the Dirac equation. Our formalism goes beyond the dipole approximation and takes into account non-dipole effects of retardation and interaction with the magnetic field components of the laser beam. We predicted cross sections for the inter-shell trielectronic recombination (TR) and quadruelectronic recombination processes which have been experimentally confirmed in electron beam ion trap measurements, mainly for C-like ions, of Ar, Fe and Kr. For Kr30+, inter-shell TR contributions of nearly 6% to the total resonant photorecombination rate were found.
The spectrum of resonance fluorescence is calculated for a two-level system excited by an intense, ultrashort x-ray pulse made available, for instance, by free-electron lasers such as the Linac Coherent Light Source. We allow for inner-shell hole decay widths and destruction of the system by further photoionization. This two-level description is employed to model neon cations strongly driven by x rays tuned to the $1s2{p}^{\ensuremath{-}1}\ensuremath{\rightarrow}1{s}^{\ensuremath{-}1}2p$ transition at 848eV848\phantom{\rule{0.28em}{0ex}}\phantom{\rule{0.16em}{0ex}}\mathrm{eV}848eV; the x rays induce Rabi oscillations which are so fast that they compete with Ne 1s1s1s-hole decay. We predict resonance fluorescence spectra for two different scenarios: first, chaotic pulses based on the self-amplified spontaneous emission principle, like those presently generated at x-ray free-electron-laser facilities and, second, Gaussian pulses which will become available in the foreseeable future with self-seeding techniques. As an example of the exciting opportunities derived from the use of seeding methods, we predict, in spite of the above obstacles, the possibility to distinguish at x-ray frequencies a clear signature of Rabi flopping in the spectrum of resonance fluorescence.
Electron spin dynamics in Kapitza-Dirac scattering from a standing laser wave of high frequency and high intensity is studied. We develop a fully relativistic quantum theory of the electron motion based on the time-dependent Dirac equation. Distinct spin dynamics, with Rabi oscillations and complete spin-flip transitions, is demonstrated for Kapitza-Dirac scattering involving three photons in a parameter regime accessible to future high-power x-ray laser sources. The Rabi frequency and, thus, the diffraction pattern is shown to depend crucially on the spin degree of freedom.