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Marko Horbatsch

Publications and source records attributed to Marko Horbatsch.

At least 19 recordsLinked to original sources

A criterion for an effective discretization of a continuous Schr\"odinger spectrum using a pseudostate basis

We consider a Hamiltonian $\hat H$ with a (partially) continuous spectrum and examine the zero-overlap condition which involves the projection onto exact continuum eigenstates of a set of pseudostates obtained from the diagonalization of $\hat H$ in a finite basis of square-integrable functions. For each projected pseudostate the condition implies the occurrence of zeros at all energies that correspond to the pseudo-continuum matrix eigenvalues, except for the eigenenergy associated with that pseudostate. This feature was observed for the Coulomb continuum represented in a Laguerre basis [M. McGovern et al., Phys. Rev. A 79, 042707 (2009)] and later explained using special properties of the Laguerre functions [I. B. Abdurakhmanov et al., J. Phys. B 44, 075204 (2011)]. We establish that a sufficient condition for the zero-overlap condition to occur is that the image space of the operator $\hat Q \hat H \hat P$, where $\hat P$ is the projection operator onto the subspace spanned by the basis and $\hat Q = \hat 1 - \hat P$ its complement, has dimension one. We show that the condition is met for the one-dimensional free-particle problem by a basis of harmonic oscillator eigenstates and by a minimal set of simple momentum-space wave functions, and for the Coulomb problem by a Laguerre basis, thus offering an alternative proof for the latter case. The zero-overlap condition ensures that in, e.g., an ionizing collision or laser-atom interaction process, transition probabilities obtained from the projection of a time-propagated pseudostate-expanded system wave function onto eigenstates of $ \hat H $ are asymptotically stable.

physics.atom-ph

A generalized independent atom model approach for net ionization of molecules by multiply-charged heavy-ion impact

The previously applied independent atom model (IAM) for highly charged ion-molecule collisions which implemented the suppression of multiple ionization and capture on the basis of geometric overlaps of cross-sectional areas representing ion-atom cross sections using a pixel counting method (PCM), [Phys. Rev. A {\bf 101}, 062709 (2020)] is extended to incorporate the possibility of multiple collisions within the molecule. This is accomplished on the basis of estimated mean free paths for sequential projectile-atom collisions. The IAM-PCM was demonstrated to be successful in describing proton-molecule collisions, and moderately-charged ion impact at high collision energies. The new model does agree with these results, but has important consequences for highly charged projectiles providing larger cross sections than IAM-PCM, but still well below the simple additivity rule results.

physics.atom-ph

The Independent Atom Model -- Pixel Counting Method for Ion-Molecule Collisions

The independent atom model - pixel counting method (IAM-PCM) for the description of ion-molecule collisions is reviewed. The method was introduced (in 2016) to improve on the simple additivity rule according to which scattering cross sections for a molecular target can be obtained by summing up the cross sections of the constituent atoms. The key idea of the IAM-PCM is the inclusion of weight factors in the summation, to be determined from a geometrical interpretation of the resultant cross section as a combined area of overlapping atomic contributions, which is calculated via a pixelization technique. We argue here that the IAM-PCM can be conceptualized in a different but equivalent way by associating each pixel in the area decomposition with a scattering event. The calculation of net and charge-state correlated capture and ionization cross sections is explained, and results for 10 keV to 10 MeV proton impact are discussed for a number of targets ranging from compact ten-electron systems to large biomolecules. A previously observed scaling behaviour of the net ionization cross sections is revisited and shown to be captured by a simple parametrization with remarkable accuracy.

physics.atom-ph

Calculation of DC Stark Resonances for the Ammonia Molecule

A model potential previously developed for the ammonia molecule is treated in a single-center partial-wave approximation in analogy with a self-consistent field method developed by Moccia. The latter was used in a number of collision studies. The model potential is used to calculate dc Stark resonance parameters, i.e., resonance positions and shifts within a single-center partial wave expansion, using the exterior complex scaling method for the radial coordinate. Three molecular valence orbitals are investigated for fields along the three Cartesian coordinates, i.e., along the molecular axis and in two perpendicular directions. The work extends previous work on the planar-geometry water molecule for which non-monotonic shifts were observed. We find such non-monotonic shifts for fields along the molecular axis. For perpendicular fields we report the splitting of the 1e orbitals into a fast- and a slow-ionizing orbital.

physics.chem-ph

Classical-trajectory model for ionizing proton-ammonia molecule collisions: the role of multiple ionization

We use an independent electron model with semi-classical approximation to electron dynamics to investigate differential cross sections for electron emission in fast collisions of protons with ammonia molecules. An effective potential model for the electronic orbitals is introduced, and utilized in the context of the classical-trajectory Monte Carlo (CTMC) approach for single-electron dynamics. Cross sections differential in electron emission angle and energy are compared with experimental data. Compared to previous scattering-theory based quantum-mechanical results the time-dependent semi-classical CTMC approach provides results of similar quality for intermediate and high ionized electron energies. We find some discrepancies in the total cross sections for $q$-fold ionization between the present model and independent-atom-model calculations. The double ionization cross sections are considerably larger than recent experimental data which are derived from coincidence counting of charged fragments. The calculated triple ionization cross sections exceed the experimental coincidence data for $q=3$ by several orders of magnitude at intermediate energies.

physics.atom-ph

Fitting for the energy levels of hydrogen

Atomic hydrogen energy levels calculated to high precision are required to assist experimental researchers working on spectroscopy in the pursuit of testing quantum electrodynamics (QED) and probing for physics beyond the Standard Model. There are two important parts to the problem of computing these levels: an accurate evaluation of contributions from QED and using an accurate value for the proton charge radius as an input. Recent progress on QED corrections to the fine structure, as well as increasing evidence that a proton charge radius in the range of 0.84 fm is favored over the previously adopted larger value in the 0.88 fm range, has advanced the field, yet several state-of-the-art measurements remain in contradiction with this smaller value. Motivated by on-going and future work in this area, we present here a simple parameterization for the energy levels of hydrogen at the level of hyperfine structure using the so-called relativistic Ritz approach. The fitting of a finite sample of QED-generated levels at low to intermediate principal quantum number, $n$, gives a generally applicable formula for \emph{all} values of $n$ for each distinct angular momentum channel, given in this work up to orbital angular momentum number $\ell=30$. We also provide a simple linear parameterization for the shift in hydrogen energy levels as a function of the proton radius, providing a useful cross check for extant and future measured energy intervals.

physics.atom-ph

Classical-trajectory time-dependent mean-field theory for ion-molecule collision problems

A mean-field model to describe electron transfer processes in ion-molecule collisions at the $\hbar =0$ level is presented and applied to collisions involving water and ammonia molecules. Multicenter model potentials account for the molecular structure and geometry. They include charge screening parameters which in the most advanced version of the model depend on the instantaneous degree of ionization so that dynamical screening effects are taken into account. The work is implemented using the classical-trajectory Monte Carlo method, i.e., Hamilton's equations are solved for classical statistical ensembles that represent the initially populated orbitals. The time-evolved trajectories are sorted into ionizing and electron capture events, and a multinomial analysis of the ensuing single-particle probabilities is employed to calculate differential and total cross sections for processes that involve single- and multiple-electron transitions. Comparison is made with experimental data and some previously reported calculations to shed light on the capabilities and limitations of the approach.

physics.atom-ph

Independent atom model description of multiple ionization of water, methane, and ammonia molecules by proton impact

We study multiple ionization in proton collisions with water, methane, and ammonia molecules using an independent-atom model. Previous work on total (net) capture and ionization cross sections is extended to treat the multiple ionization channels explicitly. We present the theoretical framework to treat charge-state correlated processes within the independent-atom model approach which uses the geometric screening introduced for different molecular geometries and orientations. Comparison of results is made for the target molecules $\rm H_2O, CH_4, NH_3$ with an emphasis on $q$-fold electron removal. Coincident measurements of produced molecular fragments can be used to estimate this quantity. We find very good agreement for the model calculations for the water molecule, where data exist for $q=1-4$. For methane we observe reasonable agreement with $q=1,2$, and for ammonia only for $q=1$, i.e., the experimental data show little support for a direct multiple ionization channel in the latter case.

physics.atom-ph

Non-monotonic dc Stark shifts in the rapidly ionizing orbitals of the water molecule

We extend a previously developed model for the Stark resonances of the water molecule. The method employs a partial-wave expansion of the single-particle orbitals using spherical harmonics. To find the resonance positions and decay rates, we use the exterior complex scaling approach which involves the analytic continuation of the radial variable into the complex plane and yields a non-hermitian Hamiltonian matrix. The real part of the eigenvalues provides the resonance positions (and thus the Stark shifts), while the imaginary parts $-\Gamma/2$ are related to the decay rates $\Gamma$, i.e., the full-widths at half-maximum of the Breit-Wigner resonances. We focus on the three outermost (valence) orbitals, as they are dominating the ionization process. We find that for forces directed in the three Cartesian co-ordinates, the fastest ionizing orbital always displays a non-monotonic Stark shift. For the case of fields along the molecular axis we also compare results as a function of the number of spherical harmonics included ($\ell_{\max}=3,4$). We also compare our results to the total molecular Stark shifts for the Hartree-Fock and coupled cluster methods.

quant-ph

Partial-wave approach to the Stark resonance problem of the water molecule

A partial-wave method is developed to deal with small molecules dominated by a central atom as an extension of earlier single-center methods. In particular, a model potential for the water molecule is expanded over a basis of spherical harmonics. A finite element method is employed to generate local polynomial functions in subintervals over a finite range for the radial variable. The angular parts of the system are represented by spherical harmonics. The problem of Stark resonances is treated with the exterior complex scaling method which incorporates a wavefunction discontinuity at the scaling radius. The resultant non-hermitian matrix eigenvalue problem yields resonance positions and widths (decay rates). We present these DC Stark shifts and exponential decay rates for the valence orbitals $1b_1$, $3a_1$, and the bonding orbital $1b_2$. Furthermore, comparison is made with total molecular decay rates and DC shifts obtained recently within the Hartree-Fock and coupled-cluster approaches.

physics.chem-ph

Classical versus quantum calculation of radiative electric quadrupole transition rates for hydrogenic states

The semiclassical Kepler-Coulomb problem and the quantum-mechanical Schr\"odinger-Coulomb problem are compared for their predictions of quadrupole E2 transitions. The semiclassical treatment involves an extension of previous work for the electric dipole transitions (Physical Review A 71, 020501), and rates are derived for $\Delta \ell= 0, \pm 2$ transitions on the basis of the multipolar properties of the emitted radiation. For the quantum case a derivation is presented within the Schr\"odinger framework without reference to spin. Comparison of the E2 rates shows reasonable agreement, but not as good as was found for the electric dipole case.

quant-ph

Calculation of Energy Loss in Antiproton Collisions with Many-Electron Systems using Ehrenfest's Theorem

Energy loss in collisions of charged projectiles with many-electron systems can be dealt with in time-dependent density functional theory by invoking Ehrenfest's theorem for the time evolution of expectation values of observables. We derive an exact expression for the evaluation of energy loss for systems described in a target reference frame, which is a functional of the electron density. Using an approximation scheme we then apply the expression to antiproton-atom collisions at intermediate and high energies within the framework of the basis generator method. The calculations are performed within the semiclassical approximation for the nuclear motion, and a straight-line trajectory is employed. The energy loss is evaluated from an expectation value of the time derivative of the time-dependent projectile potential and avoids the problem of identifying the excited and ionized many-electron contributions in the many-electron wavefunction. There is also no need to invoke the independent-event model, since the calculations are performed within the framework of the independent-electron mean-field model. Detailed comparisons are provided for net ionization and total energy loss of antiprotons colliding with hydrogen, helium, neon, carbon, nitrogen and oxygen. Reasonable agreement is found with the results from one-electron and two-electron calculations for atomic hydrogen and helium, and with experiment in the latter case. For the $\bar p - \rm Ne$ system at intermediate collision energies we find discrepancies with previous work that included only single-electron transitions. The sequence of results for C, N, O, Ne allows one to paint a consistent picture which awaits experimental verification.

physics.atom-ph

Classical calculation of radiative decay rates of hydrogenic Stark states

The Kepler-Coulomb problem is solved in parabolic coordinates and the Larmor radiation problem is analyzed to complement a previous study performed for the usual representation in spherical polar coordinates. A comparison with quantum spontaneous decay rates shows that for azimuthal quantum number $m = 0$ states only transitions to nearby $n-\Delta n$ principal quantum number states are described properly by the Wentzel-Kramers-Brillouin quantized classical motions, but that for $m > 0$ reasonable results emerge for many values of $\Delta n$. A simple approximate expression for the lifetime of $m \ne 0$ states emerges from the semi-classical analysis.

physics.atom-ph

Net electron capture in collisions of multiply charged projectiles with biologically relevant molecules

A model for the description of proton collisions from molecules composed of atoms such as hydrogen, carbon, nitrogen, oxygen and phosphorus (H, C, N, O, P) was recently extended to treat collisions with multiply charged ions with a focus on net ionization. Here we complement the work by focusing on net capture. The ion-atom collisions are computed using the two-center basis generator method. The atomic net capture cross sections are then used to assemble two models for ion-molecule collisions: an independent atom model (IAM) based on the Bragg additivity rule (labeled IAM-AR), and also the so-called pixel-counting method (IAM-PCM) which introduces dependence on the orientation of the molecule during impact. The IAM-PCM leads to significantly reduced capture cross sections relative to IAM-AR at low energies, since it takes into account the overlap of effective atomic cross sectional areas. We compare our results with available experimental and other theoretical data focusing on water vapor (H2O), methane (CH4) and uracil (C4H4N2O2). For the water molecule target we also provide results from a classical-trajectory Monte Carlo approach that includes dynamical screening effects on projectile and target. For small molecules dominated by a many-electron atom, such as carbon in methane, or oxygen in water we find a saturation phenomenon for higher projectile charges (Q = 3) and low energies, where the net capture cross section for the molecule is dominated by the net cross section for the many-electron atom, and the net capture cross section is not proportional to the total number of valence electrons.

physics.atom-ph

Non-perturbative scaling behavior for net ionization of biologically relevant molecules by multiply-charged heavy-ion impact

A recently developed model to describe proton collisions from molecules involving basic atoms such as hydrogen, carbon, nitrogen, oxygen and phosphorus (H, C, N, O, P) is extended to treat collisions with multiply charged ions. The ion-atom collisions are computed using the two-center basis generator method (TC-BGM), which has a proven track record of yielding accurate total cross sections for electron capture and ionization. The atomic net ionization cross sections are then used to assemble two models for ion-molecule collisions: an independent atom model (IAM) that follows the Bragg additivity rule (labeled IAM-AR), and also the so-called pixel-counting method (IAM-PCM). The latter yields reduced cross sections relative to IAM-AR near the maximum, since it takes into account the overlapping nature of effective cross sectional areas. The IAM-PCM for higher-charge projectiles leads to strong reductions of net ionization cross sections relative to the IAM-AR method, and is computed directly for projectile charges $Q=1, 2, 3$. The scaling behavior of the IAM-PCM is investigated over a wide range of energies $E$, and at high $E$ it converges towards the IAM-AR. An empirical scaling rule is established which allows to reproduce these results based on proton impact calculations. Detailed comparisons are provided for the uracil target ($\rm C_4 H_4 N_2 O_2$), for which other theoretical as well as experimental results are available. Based on the scaling model derived from the IAM-PCM data it is shown how the experimental data for uracil and water bombarded by multiply charged ions can be reduced to effective $Q=1$ cross sections respectively, and these are compared to proton impact data.

physics.atom-ph

Multi-charged ion-water molecule collisions in a classical-trajectory time-dependent mean-field theory

A recently proposed classical-trajectory dynamical screening model for the description of multiple ionization and capture during ion-water molecule collisions is extended to incorporate dynamical screening on both the multi-center target potential and the projectile ion. Comparison with available experimental data for He$^{2+}$ + H$_2$O collisions at intermediate energies (10-150 keV/u) and Li$^{3+}$ + H$_2$O at higher energies (100-850 keV/u) demonstrates the importance of both screening mechanisms. The question of how to deal with the repartitioning of the capture flux into allowed capture channels is addressed. The model also provides insights for data on highly-charged projectile ions (C$^{6+}$, O$^{8+}$, Si$^{13+}$) in the MeV/u range where the question of saturation effects in net ionization was raised in the literature.

physics.atom-ph

Properties of the Sachs electric form factor of the proton on the basis of recent $e-p$ scattering experiments and hydrogen spectroscopy

Recently published data on the Sachs electric form factor by the PRad collaboration (Nature {\bf 575}, 147-151) are analyzed to investigate their consistency with the known proton charge radius from muonic and electronic hydrogen spectroscopy, as well as theoretical predictions from dispersively improved chiral perturbation theory. It is shown that the latter is fully consistent with the data, and pointers are given how future $e-p$ scattering experiments can lead to an improvement of our knowledge of the form factor in the low-momentum-transfer regime.

nucl-ex

Classical-trajectory Monte Carlo calculations of differential electron emission in fast heavy-ion collisions with water molecules

A classical description of electron emission differential ionization cross sections for highly-charged high-velocity ions ($\sim$ 10 a.u.) impinging on water molecules is presented. We investigate the validity of the classical statistical mechanics description of ionization ($\hbar=0$ limit of quantum mechanics) in different ranges of electron emission energy and solid angle, where mechanisms such as soft and binary collisions are expected to contribute. The classical-trajectory Monte Carlo method is employed to calculate doubly and singly differential cross sections for C$^{6+}$, O$^{8+}$ and Si$^{13+}$ projectiles, and comparisons with Continuum Distorted Wave Eikonal Initial State theoretical results and with experimental data are presented. We implement a time-dependent screening effect in our model, in the spirit of mean-field theory to investigate its effect for highly charged projectiles. We also focus on the role of an accurate description of the molecular target by means of a three-center potential to show its effect on differential cross sections. Very good agreement with experiments is found at medium to high electron emission energies.

physics.atom-ph