Two‐electron processes in atom‐photon interactions have been studied. Various mechanisms of double photoionization, angular correlations, total cross sections, energy distributions and results for non‐Helium like systems are discussed.
Until recently, the nonlinear interaction between light and matter has been restricted to only low photon energies produced by optical lasers. However, about a decade ago, the rise of free-electron laser facilities revolutionized the field of nonlinear light-matter interaction by delivering intense high-energy light pulses. Today, such lasers are used for research in materials science, chemical technology, biophysical science, solid state physics as well as fundamental research. It is the new experimental possibilities provided by free-electron lasers that motivated the work presented in this thesis. Two-photon ionization process is one of the simplest nonlinear interactions in which absorption of two photons by an atom (or a molecule) leads to promoting one of its bound electrons to continuum. This work presents studies of two-photon ionization of neutral atoms. After a brief historical introduction to the topic of nonlinear light-matter interaction, the density matrix describing the state of an atom and a photoelectron following two-photon ionization is derived. In each successive chapter, part of this density matrix is used to obtain characteristic quantities such as total two-photon ionization cross section, photoelectron angular distributions, ion polarization or degree of polarization of fluorescence photon produced by subsequent decay of the photoion. Physical properties of these quantities are studied and intriguing phenomena, such as elliptical dichroism, polarization transfer as well as relativistic and screening effects are investigated.
A brief review is given on development of electron-photon coincidence studies from electron impact of atoms. The theory of electron-photon correlations is outlined in detail in terms of cross sections of excited atoms and excited state charge clouds. The state of a target atom is determined by the various orientation and alignment parameters and the multipole moments of the excited atom. General considerations, such as coherence effects in impact excitation, the influence of fine and hyperfine structures in correlations are taken into account. The relationship between scattering amplitudes (including their phases) and target parameters is worked out for singlet and doublet transitions.
We investigate the two-photon double ionization of beryllium atom induced by ultrashort pulses. We use a time-dependent formalism to evaluate the ionization amplitudes and generalized cross sections for the ejection of the 2s2 valence shell electrons in the presence of a fully occupied 1s2 frozen core shell. The relative contributions of the two-photon direct and sequential process are systematically explored by varying both pulse duration and central frequency. The energy and angular differential ionization yields reveal the signatures of both mechanisms, as well as the role of electron correlation in both the single and double ionization continua. In contrast with previous results on the helium atom, the presence of an electronic core strongly affects the final state leading to back-to-back electron emission even in the a priori less correlated two-photon sequential mechanism. In particular, a dominant pathway via excitation ionization through the Be+(2p) determines the profiles and pulse-duration dependencies of the energy and angle differential yields.
We report in detail our complete characterization of atomic photoionization via a single measurement, namely, that of the two-photon photoelectron angular distribution using elliptically polarized light. Through these measurements we are able to determine the atomic parameters necessary to unambiguously describe two-photon ionization of atomic rubidium. These parameters include relative cross sections for photoionization into various outgoing channels as well as the phase difference between the continuum S and D partial waves. We present a derivation of the angular distribution with arbitrarily polarized light in terms of these cross sections and phases, demonstrate the advantages of using elliptically polarized light, discuss details of the experiment, and report the results of our measurements in this paper. While measured phase differences are in excellent agreement with expected values over the entire range of photoelectron kinetic energy of our measurements from 0 to 0.5 eV, ratios of cross sections for photoionization into the two D channels are anomalous, suggesting unexpected fine structure effects in these continua.