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Lidija Andric

Bio: Lidija Andric is an academic researcher from University of Paris. The author has contributed to research in topics: Ionization & Photoionization. The author has an hindex of 17, co-authored 70 publications receiving 1073 citations. Previous affiliations of Lidija Andric include Centre national de la recherche scientifique & Pierre-and-Marie-Curie University.


Papers
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Journal ArticleDOI
TL;DR: A magnetic bottle spectrometer of the type recently developed by Eland et al. has been implemented for use with synchrotron radiation, allowing multidimensional electron spectroscopy as mentioned in this paper.
Abstract: A magnetic bottle spectrometer of the type recently developed by Eland et al [Phys Rev Lett 90, 053003 (2003)] has been implemented for use with synchrotron radiation, allowing multidimensional electron spectroscopy Its application to the Xe 4d double Auger decay reveals all the energy pathways involved The dominant path is a cascade process with a rapid (6 fs) ejection of a first Auger electron followed by the slower (>23 fs) emission of a second Auger electron Weaker processes implying 3 electron processes are also revealed, namely, direct double Auger and associated Rydberg series

102 citations

Journal ArticleDOI
TL;DR: Detailed properties are presented such as the spectroscopy, formation, and decay dynamics of the N(2)(2+) K(-2) main and satellite states and the strong chemical shifts of double K holes on an oxygen atom in CO, CO2, and O2 molecules.
Abstract: The formation of hollow molecules (with a completely empty K shell in one constituent atom) through single-photon core double ionization has been demonstrated using a sensitive magnetic bottle experimental technique combined with synchrotron radiation. Detailed properties are presented such as the spectroscopy, formation, and decay dynamics of the N(2)(2+) K(-2) main and satellite states and the strong chemical shifts of double K holes on an oxygen atom in CO, CO2, and O2 molecules.

79 citations

Journal ArticleDOI
TL;DR: A simple theoretical model based on the knockout mechanism gives reasonable agreement with experiment on the formation in a single-photon transition of two core holes, each at a different carbon atom of the C2H2 molecule.
Abstract: We observe the formation in a single-photon transition of two core holes, each at a different carbon atom of the C2H2 molecule. At a photon energy of 770.5 eV, the probability of this 2-site core double ionization amounts to 1.6 ± 0.4% of the 1-site core double ionization. A simple theoretical model based on the knockout mechanism gives reasonable agreement with experiment. Spectroscopy and Auger decays of the associated double core hole states are also investigated.

70 citations

Journal ArticleDOI
TL;DR: In this paper, the angular distributions of the vibrationally inelastic peaks were measured for n−propane and cyclopropane and the results indicated that the major cause of the dramatic differences in spectral appearance between linear and cyclic alkanes are not major changes of resonant energies, but decrease of their (lifetime-determined) width, caused by higher symmetry, rigidity, and consequently larger contribution of partial waves with high l to the scattering.
Abstract: Electron‐energy‐loss spectra in the range of vibrational excitation, and excitation functions for selected vibrational peaks, were measured for the title compounds. Angular distributions of the vibrationally inelastic peaks were measured for n‐propane and cyclopropane. The results in n‐propane are similar to the published results in ethane, only one very broad band is observed in all channels, with gradual onset at about 3 eV and a maximum around 8 eV. In contrast, narrower resonances emerge in all cyclic compounds. The effect is most pronounced in cyclopropane, where two resonances appear, at 2.6 and 5.5 eV. The latter is exceptional in several respects. It is narrow and thus relatively long lived for a shape resonance of this energy. It causes ring stretch excitation with very high selectivity and pronounced angular distribution, which is reproduced very well by the theory of Read and Andrick, revealing dominance of a partial wave with an unusually high angular momentum, l=3, m=3, and unambiguously identifying the resonance as a2′. The resonances in ethylene oxide are similar, but somewhat broader and shifted to 3 and 4.8 eV, respectively. Resonances in cyclopentane and cyclohexane resemble loosely the cyclopropane case. It is concluded that the major cause of the dramatic differences in spectral appearance between linear and cyclic alkanes are not major changes of resonant energies, but decrease of their (lifetime‐determined) width, caused by higher symmetry, rigidity, and consequently larger contribution of partial waves with high l to the scattering. This implies that the vertical electron affinity of linear alkanes is not around −8 eV, as could be assumed from the position of the peak in the attachment spectra, but higher, around −3 eV.

67 citations

Journal ArticleDOI
TL;DR: In this paper, the emission of one or two Auger electrons, following inner-shell ionization by synchrotron light, has been investigated both experimentally and theoretically, and all electrons emitted in the process are detected in coincidence and analyzed in energy thanks to a magnetic-bottle electron time-of-flight spectrometer.
Abstract: The emission of one or two Auger electrons, following Kr $3d$ inner-shell ionization by synchrotron light, has been investigated both experimentally and theoretically. All electrons emitted in the process are detected in coincidence and analyzed in energy thanks to a magnetic-bottle electron time-of-flight spectrometer. In addition, noncoincident high-resolution electron spectra have been measured to characterize the cascade double-Auger paths more fully. Combination of the two experimental approaches and of our calculations allows a full determination of the decay pathways and branching ratios in the case of Kr $3d$ single- and double-Auger decays. The ${\mathrm{Kr}}^{3+}$ threshold is found at $74.197\ifmmode\pm\else\textpm\fi{}0.020$ eV.

64 citations


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TL;DR: In this article, the authors present the landmarks of the 30-odd-year evolution of ultrashort-pulse laser physics and technology culminating in the generation of intense few-cycle light pulses and discuss the impact of these pulses on high-field physics.
Abstract: The rise time of intense radiation determines the maximum field strength atoms can be exposed to before their polarizability dramatically drops due to the detachment of an outer electron. Recent progress in ultrafast optics has allowed the generation of ultraintense light pulses comprising merely a few field oscillation cycles. The arising intensity gradient allows electrons to survive in their bound atomic state up to external field strengths many times higher than the binding Coulomb field and gives rise to ionization rates comparable to the light frequency, resulting in a significant extension of the frontiers of nonlinear optics and (nonrelativistic) high-field physics. Implications include the generation of coherent harmonic radiation up to kiloelectronvolt photon energies and control of the atomic dipole moment on a subfemtosecond $(1{\mathrm{f}\mathrm{s}=10}^{\mathrm{\ensuremath{-}}15}\mathrm{}\mathrm{s})$ time scale. This review presents the landmarks of the 30-odd-year evolution of ultrashort-pulse laser physics and technology culminating in the generation of intense few-cycle light pulses and discusses the impact of these pulses on high-field physics. Particular emphasis is placed on high-order harmonic emission and single subfemtosecond extreme ultraviolet/x-ray pulse generation. These as well as other strong-field processes are governed directly by the electric-field evolution, and hence their full control requires access to the (absolute) phase of the light carrier. We shall discuss routes to its determination and control, which will, for the first time, allow access to the electromagnetic fields in light waves and control of high-field interactions with never-before-achieved precision.

2,547 citations

Journal ArticleDOI
TL;DR: The cold target recoil ion momentum spectroscopy (COLTRIMS) is a momentum space imaging technique for the investigation of the dynamics of ionizing ion, electron or photon impact reactions with atoms or molecules as mentioned in this paper.

985 citations

Journal ArticleDOI
05 Apr 2007-Nature
TL;DR: The real-time observation of this most elementary step in strong-field interactions: light-induced electron tunnelling is reported, and the process is found to deplete atomic bound states in sharp steps lasting several hundred attoseconds, suggesting a new technique, attose Cond Tunnelling, for probing short-lived, transient states of atoms or molecules with high temporal resolution.
Abstract: Atoms exposed to intense light lose one or more electrons and become ions. In strong fields, the process is predicted to occur via tunnelling through the binding potential that is suppressed by the light field near the peaks of its oscillations. Here we report the real-time observation of this most elementary step in strong-field interactions: light-induced electron tunnelling. The process is found to deplete atomic bound states in sharp steps lasting several hundred attoseconds. This suggests a new technique, attosecond tunnelling, for probing short-lived, transient states of atoms or molecules with high temporal resolution. The utility of attosecond tunnelling is demonstrated by capturing multi-electron excitation (shake-up) and relaxation (cascaded Auger decay) processes with subfemtosecond resolution.

753 citations

Journal ArticleDOI
TL;DR: In this article, the Fourier series for differentiable functions of higher differentiability has been studied and an alternative method of estimation has been proposed for estimating the Gibbs oscillations of the finite Fourier expansion.
Abstract: Preface Bibliography 1. Interpolation. Introduction The Taylor expansion The finite Taylor series with the remainder term Interpolation by polynomials The remainder of Lagrangian interpolation formula Equidistant interpolation Local and global interpolation Interpolation by central differences Interpolation around the midpoint of the range The Laguerre polynomials Binomial expansions The decisive integral transform Binomial expansions of the hypergeometric type Recurrence relations The Laplace transform The Stirling expansion Operations with the Stirling functions An integral transform of the Fourier type Recurrence relations associated with the Stirling series Interpolation of the Fourier transform The general integral transform associated with the Stirling series Interpolation of the Bessel functions 2. Harmonic Analysis. Introduction The Fourier series for differentiable functions The remainder of the finite Fourier expansion Functions of higher differentiability An alternative method of estimation The Gibbs oscillations of the finite Fourier series The method of the Green's function Non-differentiable functions Dirac's delta function Smoothing of the Gibbs oscillations by Fejer's method The remainder of the arithmetic mean method Differentiation of the Fourier series The method of the sigma factors Local smoothing by integration Smoothing of the Gibbs oscillations by the sigma method Expansion of the delta function The triangular pulse Extension of the class of expandable functions Asymptotic relations for the sigma factors The method of trigonometric interpolation Error bounds for the trigonometric interpolation method Relation between equidistant trigonometric and polynomial interpolations The Fourier series in the curve fitting 3. Matrix Calculus. Introduction Rectangular matrices The basic rules of matrix calculus Principal axis transformation of a symmetric matrix Decomposition of a symmetric matrix Self-adjoint systems Arbitrary n x m systems Solvability of the general n x m system The fundamental decomposition theorem The natural inverse of a matrix General analysis of linear systems Error analysis of linear systems Classification of linear systems Solution of incomplete systems Over-determined systems The method of orthogonalisation The use of over-determined systems The method of successive orthogonalisation The bilinear identity Minimum property of the smallest eigenvalue 4. The Function Space. Introduction The viewpoint of pure and applied mathematics The language of geometry Metrical spaces of infinitely many dimensions The function as a vector The differential operator as a matrix The length of a vector The scalar product of two vectors The closeness of the algebraic approximation The adjoint operator The bilinear identity The extended Green's identity The adjoint boundary conditions Incomplete systems Over-determined systems Compatibility under inhomogeneous boundary conditions Green's identity in the realm of partial differential operators The fundamental field operations of vector analysis Solution of incomplete systems 5. The Green's Function. Introduction The role of the adjoint equation The role of Green's identity The delta function -- The existence of the Green's function Inhomogeneous boundary conditions The Green's vector Self-adjoint systems The calculus of variations The canonical equations of Hamilton The Hamiltonisation of partial operators The reciprocity theorem Self-adjoint problems Symmetry of the Green's function Reciprocity of the Green's vector The superposition principle of linear operators The Green's function in the realm of ordinary differential operators The change of boundary conditions The remainder of the Taylor series The remainder of the Lagrangian interpolation formula

554 citations

Journal ArticleDOI
TL;DR: In this article, high-resolution recoil-ion momentum spectroscopy (RIMS) is used to determine the charge state and the complete final momentum vector of a recoiling target ion emerging from an ionizing collision of an atom with any kind of radiation.
Abstract: High-resolution recoil-ion momentum spectroscopy (RIMS) is a novel technique to determine the charge state and the complete final momentum vector of a recoiling target ion emerging from an ionizing collision of an atom with any kind of radiation. It offers a unique combination of superior momentum resolution in all three spatial directions of with a large detection solid angle of . Recently, low-energy electron analysers based on rigorously new concepts and reaching similar specifications were successfully integrated into RIM spectrometers yielding so-called `reaction microscopes'. Exploiting these techniques, a large variety of atomic reactions for ion, electron, photon and antiproton impact have been explored in unprecedented detail and completeness. Among them kinematically complete experiments on electron capture, single and double ionization in ion - atom collisions at projectile energies between 5 keV and 1.4 GeV have been carried out. Double photoionization of He has been investigated at energies close to the threshold up to . At the contributions to double ionization after photoabsorption and Compton scattering were separated kinematically for the first time. These and many other results will be reviewed in this paper. In addition, the experimental technique is described in some detail and emphasis is given to envisaging the rich future potential of the method in various fields of atomic collision physics with atoms, molecules and clusters.

374 citations