Density functional theory for molecular multiphoton ionization in the perturbative regime

A general implementation of the lowest nonvanishing order perturbation theory for the calculation of molecular multiphoton ionization cross sections is proposed in the framework of density functional theory. Bound and scattering wave functions are expanded in a multicentric basis set and advantage is taken of the full molecular point group symmetry, thus enabling the application of the formalism to medium-size molecules. Multiphoton ionization cross sections and angular asymmetry parameters have been calculated for the two- and four-photon ionization of the H2+ molecule, for linear and circular light polarizations. Both fixed and random orientations of the target molecule have been considered. To demonstrate the efficiency of the proposed methodology, the two-photon cross section and angular asymmetry parameters for the HOMO and HOMO-1 orbital ionization of benzene are also presented

Photoionization of endohedral atoms: Molecular and interchannel-coupling effects

Calculations of the photoionization cross section of the 2p and 3s subshells of free Ar and Ar@C-60 as examples have been performed using the molecular structure of the confined system and time-dependent density functional theory for the dynamical quantities. The results for Ar 2p in the combined system exhibit significant confinement resonances with the lower-energy ones being quite sharp, in contrast to the results of jellium-model calculations. In addition, calculations done with and without interchannel coupling between the photoionization channels of the 2p subshell of the Ar atom and the 1s subshell of the C-60 shell show that, in this case, the coupling is of negligible importance, even though the C 1s cross section is more than an order of magnitude larger than that of Ar 2p in the 300 eV range. The Ar 3s, which is not hybridized, also exhibits confinement resonances, but is very strongly affected by interchannel coupling with photoionization channels from the C-60 shell. The phenomenology of both 2p and 3s subshells is explained in terms of the interchannel-coupling matrix elements. These results should be applicable to inner-shell ionization of essentially any endohedral fullerene system

Theoretical Study of Ultrafast Electron Dynamics in Amino Acids

Prompt ioiuzatiou of large biological molecules may mince ultra fast charge migration along the molecular skeleton, preceding any unclear rearrangement[1, 2]. This phenomenon lots been recently observed in the amino acid phenylalanine [3] in a two-color pump probe experiment, where the production of ionic fragments Was measured as a function of the time delay between the two pulses and charge fluctuations manifested as sub-4.5 fs oscillations in the quantum yield of a spcific doubly charged fragment. We present our latcst results in glycine, and compare with previous findings in pheitylalanine [3]. We seek to perform a systematic study including larger aminoncids such as tryptophan

Accurate Description of Photoionization Dynamical Parameters

Calculation of dynamical parameters for photoionization requires an accurate description of the initial and final states of the system, as well as of the outgoing electron. We show that using a linear combination of atomic orbitals B-spline density functional theory (DFT) method to describe the outgoing electron, in combination with correlated equation of motion coupled cluster singles and double Dyson orbitals, gives good agreement with experiment and outperforms other simpler approaches, like plane and Coulomb waves, used to describe the photoelectron. Results are presented for cross-sections, angular distributions, and dichroic parameters in chiral molecules, as well as for photoionization from excited states. We also present a comparison with the results obtained using Hartree-Fock and DFT molecular orbitals selected according to Koopmans' theorem for the bound states

Accurate photoionisation cross section for He at non-resonant photon energies

The total single-photon ionisation cross section was calculated for helium atoms in their ground state. Using a full configuration-interaction approach the photoionisation cross section was extracted from the complex-scaled resolvent. In the energy range from ionisation threshold to 59\,eV our results agree with an earlier $B$-spline based calculation in which the continuum is box discretised within a relative error of $0.01\%$ in the non-resonant part of the spectrum. Above the \He^{++} threshold our results agree on the other hand very well to a recent Floquet calculation. Thus our calculation confirms the previously reported deviations from the experimental reference data outside the claimed error estimate. In order to extend the calculated spectrum to very high energies, an analytical hydrogenic-type model tail is introduced that should become asymptotically exact for infinite photon energies. Its universality is investigated considering also H$^-$, Li$^+$, and HeH$^+$. With the aid of the tail corrections to the dipole approximation are estimated.Comment: 20 pages, 7 figures, 2 table

Density Functional Theory for the Photoionization Dynamics of Uracil

Photoionization dynamics of the RNA base Uracil is studied in the framework of Density Functional Theory (DFT). The photoionization calculations take advantage of a newly developed parallel version of a multicentric approach to the calculation of the electronic continuum spectrum which uses a set of B-spline radial basis functions and a Kohn-Sham density functional hamiltonian. Both valence and core ionizations are considered. Scattering resonances in selected single-particle ionization channels are classified by the symmetry of the resonant state and the peak energy position in the photoelectron kinetic energy scale; the present results highlight once more the site specificity of core ionization processes. We further suggest that the resonant structures previously characterized in low-energy electron collision experiments are partly shifted below threshold by the photoionization processes. A critical evaluation of the theoretical results providing a guide for future experimental work on similar biosystems

Scattering effects from neighboring atoms in core-level WSe2 photoemission

Methods of attosecond science originally developed to investigate systems in the gas phase are currently being adapted to obtain temporal information on the electron dynamics that takes place in condensed-matter systems. In particular, streaking measurements have recently been performed to determine photoemission time delays from the WSe2 dichalcogenide. In this work we present a fully atomistic description of the photoemission process in WSe2 and provide angularly resolved photoemission cross sections and time delays from the W 4f, Se 3d and Se 4s core states of the system. Since these states are spatially localized, we propose a cluster approach in which we build up from smaller to larger clusters, so that we can assess the importance of scattering effects by each new layer of neighboring atoms. We use a static-exchange density functional theory method with B-spline functions, where a one-center angular-momentum expansion is supplemented by off-center expansions with fewer partial waves. This enhances convergence in comparison with a one-center expansion, which would require very high angular momenta to characterize the localized fast oscillations near each off-center atomic core. We find that the photoemission delays and fully differential cross sections are strongly affected by scattering events that take place off the neighboring atoms, implying the need to consider their effects for quantitative descriptions of the photoemission proces

Attosecond spectroscopy of bio-chemically relevant molecules

Understanding the role of the electron dynamics in the photochemistry of bio-chemically relevant molecules is key to getting access to the fundamental physical processes leading to damage, mutation and, more generally, to the alteration of the final biological functions. Sudden ionization of a large molecule has been proven to activate a sub-femtosecond charge flow throughout the molecular backbone, purely guided by electronic coherences, which could ultimately affect the photochemical response of the molecule at later times. We can follow this ultrafast charge flow in real time by exploiting the extreme time resolution provided by attosecond light sources. In this work recent advances in attosecond molecular physics are presented with particular focus on the investigation of bio-relevant molecules

Strong field ionization to multiple electronic states in water

High harmonic spectra show that laser-induced strong field ionization of water has a significant contribution from an inner-valence orbital. Our experiment uses the ratio of H2O and D2O high harmonic yields to isolate the characteristic nuclear motion of the molecular ionic states. The nuclear motion initiated via ionization of the highest occupied molecular orbital (HOMO) is small and is expected to lead to similar harmonic yields for the two isotopes. In contrast, ionization of the second least bound orbital (HOMO-1) exhibits itself via a strong bending motion which creates a significant isotope effect. We elaborate on this interpretation by simulating strong field ionization and high harmonic generation from the water isotopes using the time-dependent Schr\"odinger equation. We expect that this isotope marking scheme for probing excited ionic states in strong field processes can be generalized to other molecules