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Near threshold electron-impact double ionization of helium
We examine the break-up pattern for the electron-impact double ionization of helium using a time-dependent close-coupling approach. This ionization process is one of the simplest examples of the Coulomb four-body problem of three charged particles moving in the Coulomb field of a bare nucleus. Studies of this four-body process in the near-threshold region allow exploration of the break-up dynamics, which have been stimulated by differing predictions of the most likely geometries for break-up in the related processes of triple photoionization of lithium and electron-impact double ionization of helium. While both processes lead to the same final state of three electrons moving in the field of a bare nucleus, the preferred break-up pattern at low energies for the triple photoionization is predicted as a T-shape (Emmanouilidou et al 2008 Phys. Rev. Lett. 100 063002; Colgan et al 2013 Phys. Rev. Lett. 110 063001) and for the electron-impact double ionization as a 'triangle' pattern (Ren et al 2008 Phys. Rev. Lett. 101 093201). Our calculations at an excess energy of 5 eV show that a triangle break-up pattern is favored, confirming earlier experimental results (Ren et al 2008 Phys. Rev. Lett. 101 093201).
Interference in electron–molecule elastic scattering
General formulas describing the multiple scattering of electron by polyatomic molecules have been derived within the framework of the model of non-overlapping atomic potentials. These formulas are applied to different carbon molecules, both for fixed-in-space and randomly oriented molecules. Here, the molecular continuum wave function is represented as a plane wave plus a linear combination of the Green’s functions for free motion and the derivatives of these functions. Far from the target the electron spherical waves interfere as in the case of the Young’s double slits experiment. This interference manifests itself as diffraction oscillations in the differential and total cross sections for elastic electron scattering. The amplitude of electron scattering by a molecule is defined by the phase shifts for each of the atoms forming the target and its geometry. The numerical calculation of the scattering amplitude in closed form (rather than in the form of S-matrix expansion) is reduced to solving a system of algebraic equations. The number of atoms in a molecule and the atomic phase shifts for the orbital angular momenta included in the calculation define the number of equations.
Proton impact excitation of the Na atom
A time-dependent close-coupling (TDCC) method is developed and used to calculate proton impact excitation cross sections for atoms. Cross sections for $3s\to {nl}$ excitations of the Na atom are calculated for proton impact energies ranging from 1.0 to 100.0 keV. The TDCC cross sections are found to be in agreement for some energies with recommended cross sections from overall fits to theoretical and experimental atomic data.
The role of excited-state ionization on the effective ionization of neutral neon using non-perturbative atomic data
With the aim of providing accurate atomic data for plasma edge temperature and density modeling with neutral neon, new non-perturbative R-Matrix with Pseudostates (RMPS) calculations are performed for both the electron-impact excitation and ionization of neutral neon. The new calculations agree well with past measurements and calculations for both electron-impact excitation and ionization. For ionization, the addition of pseudostates from $5\bar{d}$ to $12\bar{i}$ allows us to extract new cross sections and rate coefficients for all of the excited states through 2p 5 5p. The new RMPS ionization calculation gives a 20% increase in the cross section for the $2{p}^{5}5s$ ionization compared with previous non-perturbative calculations and shows classically-expected n 4 -scaled convergence for the np and nd valence shells. Ionization from these excited states contributes significantly to the effective ionization rate coefficient: a factor of three more than the ground-state ionization rate coefficient at an electron temperature of 25 eV and density of 1014 cm -3 . An accurate, non-perturbative set of atomic rates, both LS- and LSJ-resolved, for neutral neon across a wide range of temperatures and densities is compiled.
Time-resolved quantum beats in the fluorescence of helium resonantly excited by XUV radiation
Abstract We report on the observation of time-resolved quantum beats in the helium fluorescence from the transition 1 s 3 p → 1 s 2 s , where the initial state is excited by XUV free electron laser radiation. The quantum beats originate from the Zeeman splitting of the magnetic substates due to an external magnetic field. We perform a systematic study of this effect and discuss the possibilities of studying this phenomenon in the XUV and x-ray regime.
Single photon simultaneous K-shell ionization/excitation in C 6 H 6 : experiment and theory
Single photon simultaneous core ionization/core excitation (K -2 V) of the Benzene molecule has been observed experimentally, using synchrotron radiation, by electron coincidence spectroscopy with a magnetic bottle time-of-flight electron spectrometer and reveals a rich spectrum. DFT and Post–Hartree–Fock calculations provide detailed assignments of K -2 V states. The specific Auger decay of these states has also been determined experimentally with a new technique to improve the energy resolution.
Imaging multiphoton ionization dynamics of CH 3 I at a high repetition rate XUV free-electron laser
XUV multiphoton ionization of molecules is commonly used in free-electron laser experiments to study charge transfer dynamics. However, molecular dissociation and electron dynamics, such as multiple photon absorption, Auger decay, and charge transfer, often happen on competing time scales, and the contributions of individual processes can be difficult to unravel. We experimentally investigate the Coulomb explosion dynamics of methyl iodide upon core–hole ionization of the shallow inner-shell of iodine (4d) and classically simulate the fragmentation by phenomenologically introducing ionization dynamics and charge transfer. Under our experimental conditions with medium fluence and relatively long XUV pulses (~75 fs), we find that fast Auger decay prior to charge transfer significantly contributes to the charging mechanism, leading to a yield enhancement of higher carbon charge states upon molecular dissociation. Furthermore, we argue for the existence of another charging mechanism for the weak fragmentation channels leading to triply charged carbon atoms. This study shows that classical simulations can be a useful tool to guide the quantum mechanical description of the femtosecond dynamics upon multiphoton absorption in molecular systems.
Dissociative electron attachment studies of gas-phase acetic acid using a velocity map imaging technique
Abstract Advancing instrumentation to explore dissociative electron attachment (DEA) studies allows previously unattainable information to be acquired. Using a newly constructed velocity map imaging spectrometer, we revisited a study on DEA to gas-phase acetic acid. We discuss possible fragmentation channels and compared the corresponding ion yields with previous high electron-energy resolution results. We focus on the channels occurring at higher energies, particularly near 10 eV, and calculate their thermodynamic thresholds. Moreover, we expand previous studies and perform time-sliced imaging near the 10 eV resonance to obtain the kinetic energy distribution of the fragment ions.
Quantum dynamics of positron-hydrogen scattering and three-body bound state formation with an assisting laser field: predictions of a reduced-dimensionality model
Abstract We investigate the quantum dynamics of target excitation and positronium formation in the positron-hydrogen atom scattering without and with an external assisting laser field within a reduced-dimensional quantum model. Strong interference fringes between the incident and reflected positron wave packets are observed in the reaction region. We further investigate the critical behavior of transition probabilities near the channel-opening thresholds for hydrogen excitation and positronium formation and find a strong competition between channels with similar threshold energies, but different parities. The transmission ratios of the incident positron in different reaction channels are calculated, and it is shown that only positronium formation in the ground state prefers forward scattering. Our simulation of the positron-hydrogen scattering with an assisting laser field indicates that the three-particle bound states can be formed during the collisions due to the photon emission induced by the external laser field.
Dipolar focusing in laser-assisted positronium formation
Abstract We consider positronium formation in collisions of positrons with excited hydrogen atoms H(n) in an infrared laser field theoretically. This process is assisted by the dipolar focusing effect: a positron moving in a superposition of a laser field and the dipolar field can approach the atomic target even if its trajectory starts with a very large impact parameter, leading to a significant enhancement of the Ps formation cross section. The classical trajectory Monte Carlo method, which is justified for n ⩾ 3 , allows efficient calculation of this enhancement. A similar effect can occur in collisions of positrons with other atoms in excited states, which can lead to improvements in the efficiency of positronium formation.
Cooper minima in high-Z atoms: effects of correlation and relativity on np photoionization
Abstract Photoionization dipole transition matrix elements pass through a zero or attain a minimum that leaves imprints on photoionization parameters like the cross-section, angular distribution asymmetry parameter, phase shift, and photoionization time delay. This minimum is commonly known as the ‘Cooper minimum’ (CM). The CM, in general, is strongly affected by relativistic and correlation effects. Previous works investigated CM in the 6pand 5psubshell photoionization up toZ= 100 using the single-particle Dirac-Slater (DS) method. The present work extends the earlier work toZup to 120 using more accurate methods; Dirac–Hartree–Fock (DHF) which includes the relativistic effects and exchange correlations, and the relativistic random phase approximation (RRPA) which includes both initial and final state electron-electron correlations along with relativistic effects. In addition to the study of photoionization from the 6pand 5psubshells, the 4psubshell has also been investigated in the present work. To demonstrate the prominent effects in the high-Z atoms, Rn (Z= 86), Ra (Z= 88), No (Z= 102), Cn (Z = 112), Og (Z= 118), and Ubn (Z= 120) are investigated.
Ultrafast x-ray scattering and electronic coherence at avoided crossings: complete isotropic signals
Abstract Nonadiabatic transitions at conical intersections and avoided crossings play a pivotal role in shaping the outcomes of photochemical reactions. Using the photodissociation of LiF as a model, this theoretical study explores the application of gas phase nonresonant ultrafast x-ray scattering to map nonadiabatic transitions at an avoided crossing, utilizing the part of the scattering signal that probes electronic coherence directly. The presented scattering signals are rotationally averaged and calculated from two- rather than one-electron (transition) densities, which inherently accounts for all possible electronic transitions driven by the x-ray photon. This approach provides quantitative predictions of the experimental signals, thereby facilitating future experimental endeavors to observe nonadiabatic effects and coherent electron dynamics with ultrafast x-ray scattering.
Protocols for x-ray transient grating pump/optical probe experiments at x-ray free electron lasers
Abstract Transient grating spectroscopy is a specialized application of the four-wave-mixing methodology and constitutes a versatile technique for investigating the dynamics of vibrational, magnetic and electronic degrees of freedom of matter in a background-free fashion. Recent developments in free-electron laser sources have enabled the extension of this technique into the extreme ultraviolet range. Ongoing efforts to expand transient grating spectroscopy into the x-ray regime promise numerous advantages: (1) substantial penetration depths that allow for probing bulk material properties, (2) element specificity via specific core-excited states, and (3) short wavelengths that allow for excitation gratings with higher momentum transfer and improved spatial resolution. In this study, we comprehensively outline the procedures for conducting x-ray transient grating pump/optical probe experiment. The process encompasses the design and alignment of the experimental setup, as well as the subsequent steps involved in data acquisition and analysis. This paper is intended as a comprehensive guide for researchers interested in implementing x-ray transient grating spectroscopy, providing valuable insights into the intricacies of the experimental workflow required for this novel technique. Furthermore, we discuss the potential for extending this methodology to an x-ray pump/x-ray probe scheme, envisioning a future direction that holds promise for enhancing the capabilities and scope of x-ray transient grating spectroscopy, opening new opportunities for studying ultrafast processes with unprecedented temporal and spatial resolutions.