Selective bond-breaking in formic acid by dissociative electron attachment.

We report the results of a joint experimental and theoretical study of dissociative electron attachment to formic acid (HCOOH) in the 6-9 eV region, where H- fragment ions are a dominant product. Breaking of the C-H and O-H bonds is distinguished experimentally by deuteration of either site. We show that in this region H- ions can be produced by formation of two or possibly three Feshbach resonance (doubly-excited anion) states, one of which leads to either C-H or O-H bond scission, while the other can only produce formyloxyl radicals by O-H bond scission. Comparison of experimental and theoretical angular distributions of the anion fragment allows the elucidation of state specific pathways to dissociation

Turning the Table: Plants Consume Microbes as a Source of Nutrients

Interactions between plants and microbes in soil, the final frontier of ecology, determine the availability of nutrients to plants and thereby primary production of terrestrial ecosystems. Nutrient cycling in soils is considered a battle between autotrophs and heterotrophs in which the latter usually outcompete the former, although recent studies have questioned the unconditional reign of microbes on nutrient cycles and the plants' dependence on microbes for breakdown of organic matter. Here we present evidence indicative of a more active role of plants in nutrient cycling than currently considered. Using fluorescent-labeled non-pathogenic and non-symbiotic strains of a bacterium and a fungus (Escherichia coli and Saccharomyces cerevisiae, respectively), we demonstrate that microbes enter root cells and are subsequently digested to release nitrogen that is used in shoots. Extensive modifications of root cell walls, as substantiated by cell wall outgrowth and induction of genes encoding cell wall synthesizing, loosening and degrading enzymes, may facilitate the uptake of microbes into root cells. Our study provides further evidence that the autotrophy of plants has a heterotrophic constituent which could explain the presence of root-inhabiting microbes of unknown ecological function. Our discovery has implications for soil ecology and applications including future sustainable agriculture with efficient nutrient cycles

Roadmap on photonic, electronic and atomic collision physics: I. Light-matter interaction

We publish three Roadmaps on photonic, electronic and atomic collision physics in order to celebrate the 60th anniversary of the ICPEAC conference. In Roadmap I, we focus on the light-matter interaction. In this area, studies of ultrafast electronic and molecular dynamics have been rapidly growing, with the advent of new light sources such as attosecond lasers and x-ray free electron lasers. In parallel, experiments with established synchrotron radiation sources and femtosecond lasers using cutting-edge detection schemes are revealing new scientific insights that have never been exploited. Relevant theories are also being rapidly developed. Target samples for photon-impact experiments are expanding from atoms and small molecules to complex systems such as biomolecules, fullerene, clusters and solids. This Roadmap aims to look back along the road, explaining the development of these fields, and look forward, collecting contributions from twenty leading groups from the field

Variational treatment of electron-polyatomic-molecule scattering calculations using adaptive overset grids

The complex Kohn variational method for electron-polyatomic-molecule scattering is formulated using an overset-grid representation of the scattering wave function. The overset grid consists of a central grid and multiple dense atom-centered subgrids that allow the simultaneous spherical expansions of the wave function about multiple centers. Scattering boundary conditions are enforced by using a basis formed by the repeated application of the free-particle Green's function and potential Ĝ0+V on the overset grid in a Born-Arnoldi solution of the working equations. The theory is shown to be equivalent to a specific Padé approximant to the T matrix and has rapid convergence properties, in both the number of numerical basis functions employed and the number of partial waves employed in the spherical expansions. The method is demonstrated in calculations on methane and CF4 in the static-exchange approximation and compared in detail with calculations performed with the numerical Schwinger variational approach based on single-center expansions. An efficient procedure for operating with the free-particle Green's function and exchange operators (to which no approximation is made) is also described

Fully differential single-photon double photoionization of atomic magnesium

The valence-shell double ionization of atomic magnesium is calculated using a grid-based representation of the 3s2 electron configuration in the presence of a fully occupied frozen-core configuration of the remaining ten electrons. Atomic orbitals are constructed from an underlying finite-element discrete variable representation that facilitates accurate representation of the interaction between the inner-shell electrons with those entering the continuum. Length and velocity gauge results are compared with recent theoretical calculations and experimental measurements for the total double-, single-, and triple-differential cross sections, particularly at the photon energy of 55.49 eV for the last one. Comparison between the similar processes of double ionization of the ns2 atoms helium, beryllium, and magnesium further illuminates the role of valence-shell electron correlation in atomic targets with heliumlike electronic configurations and symmetry

The Connection between Resonances and Bound States in the Presence of a Coulomb Potential.

The connection between resonant metastable states and bound states with changing potential strength in the presence of a Coulomb potential is fundamentally different from the case of short-range potentials. This phenomenon is central to the physics of dissociative recombination of electrons with molecular cations. Here, it is verified computationally that there is no direct connection between the resonance pole of the S-matrix and any pole in the bound state spectrum. A detailed analysis is presented of the analytic structure of the scattering matrix, in which the resonance pole remains distinct in the complex k-plane while a new state appears in the bound state spectrum. A formulation of quantum-defect theory is developed based on the scattering matrix, which nonetheless exposes a close analytic relation between the resonant and bound state poles and thereby reveals the connection between quantum-defect theory and analytic S-matrix theory in the complex energy and momentum planes. One-channel and multichannel versions of the expressions with numerical examples for simple models are given, and the formalism is applied to give a unified picture of ab initio electronic structure and scattering calculations for e-O2+ and e-H2+ scattering

Fully differential single-photon double photoionization of atomic magnesium

The valence-shell double ionization of atomic magnesium is calculated using a grid-based representation of the 3s2 electron configuration in the presence of a fully occupied frozen-core configuration of the remaining ten electrons. Atomic orbitals are constructed from an underlying finite-element discrete variable representation that facilitates accurate representation of the interaction between the inner-shell electrons with those entering the continuum. Length and velocity gauge results are compared with recent theoretical calculations and experimental measurements for the total double-, single-, and triple-differential cross sections, particularly at the photon energy of 55.49 eV for the last one. Comparison between the similar processes of double ionization of the ns2 atoms helium, beryllium, and magnesium further illuminates the role of valence-shell electron correlation in atomic targets with heliumlike electronic configurations and symmetry

Correlated variational treatment of ionization coupled to nuclear motion: Ultrafast pump and ionizing probe of electronic and nuclear dynamics in LiH

We demonstrate a theoretical treatment of dissociative single ionization of the LiH molecule using two-color UV-UV pulse sequences that makes use of a highly correlated description of both the ionization continuum and target molecular ion and neutral states to which it is coupled. The present results emphasize how the details of the ionization process at various internuclear distances combine to form a lens through which such experiments image the dynamics of intermediate electronic states populated by the pump pulse. While ionization yields (dissociative and nondissociative) provide information about the amplitudes and phases that build up the molecular wave packet in the neutral states, molecular frame photoelectron angular distributions exhibit the changing character of those states, i.e., from ionic to covalent. In addition, the time-dependent mean kinetic energy of the wave packet on neutral states is clearly mapped onto the kinetic energy release of the atomic fragments produced by the probe ionization pulse

Optimized pulses for Raman excitation through the continuum: Verification using the multiconfigurational time-dependent Hartree-Fock method

We have verified a mechanism for Raman excitation of atoms through continuum levels previously obtained by quantum optimal control using the multiconfigurational time-dependent Hartree-Fock (MCTDHF) method. For the optimal control, which requires running multiple propagations to determine the optimal pulse sequence, we used the computationally inexpensive time-dependent configuration interaction singles (TDCIS) method. TDCIS captures all of the necessary correlation of the desired processes but assumes that ionization pathways reached via double excitations are not present. MCTDHF includes these pathways and all multiparticle correlations in a set of time-dependent orbitals. The mechanism that was determined to be optimal in the Raman excitation of the Ne 1s22s22p53p1 valence state via the metastable 1s22s12p63p1 resonance state involves a sequential resonance-valence excitation. First, a long pump pulse excites the core-hole state, and then a shorter Stokes pulse transfers the population to the valence state. This process represents the first step in a multidimensional x-ray spectroscopy scheme that will provide a local probe of valence electronic correlations. Although at the optimal pulse intensities at the TDCIS level of theory the MCTDHF method predicts multiple ionization or excitation ionization of the atom, at slightly lower intensities (reduced by a factor of about 4) the TDCIS mechanism is shown to hold qualitatively. Quantitatively, the MCTDHF populations are reduced from the TDCIS calculations by a factor of 4