Chemi-ionization Reactions Research Articles

Enthalpy of the Cerium (Ce) Chemi-Ionization Reaction and CeO+, CeC+, and CeCO+ Bond Energies Determined by Energy-Resolved Guided Ion Beam Mass Spectrometry Experiments.

Cerium (Ce) oxide, carbide, and carbonyl cation bond energies and the exothermicity of the Ce chemi-ionization (CI) reaction with atomic oxygen were investigated using guided-ion beam tandem mass spectrometry (GIBMS). The kinetic energy dependent product cross sections for reactions of Ce+ with O2, CO, and CO2 and CeO+ with O2, CO, Xe, and Ar were measured using GIBMS. For the reactions of Ce+ with O2 and CO2, CeO+ is formed through an exothermic reaction, whereas CeO+ formation is endothermic in the reaction with CO. This reaction also forms CeC+ and CeCO+ is formed in the reaction of Ce+ with CO2, both in endothermic processes. Reactions of CeO+ with all four gases led to endothermic collision-induced dissociation as well as exchange reactions to form CeO2+ for the O2 and CO reactants. Bond dissociation energies (BDEs) at 0 K were determined through analyses of the kinetic energy dependent cross sections for all endothermic reactions. We determined that the BDEs of CeO+, CeC+, and CeCO+ are 8.46 ± 0.15, 3.93 ± 0.16, and ≥0.25 ± 0.07 eV, respectively, where the CeO+ BDE is a weighted average of 6 independent 0 K threshold measurements. The CeO+ BDE is combined with the ionization energy (IE) of Ce to determine an exothermicity of 2.91 ± 0.15 eV for the Ce + O → CeO+ + e- chemi-ionization reaction. Combined with neutral BDEs from the literature, the thermochemistry determined here also provides IE(CeO) = 5.03 ± 0.12 eV and IE(CeC) = 6.50 ± 0.16 eV. Theoretical calculations for ground and some excited states were performed for CeO+, CeC+, and CeCO+ to provide insight into the bonding and a comparison with the experimentally determined BDEs for each molecule.

Collisional alignment and molecular rotation control the chemi-ionization of individual conformers of hydroquinone with metastable neon.

The relationship between the shape of a molecule and its chemical reactivity is a central tenet in chemistry. However, the influence of the molecular geometry on reactivity can be subtle and result from several opposing effects. Here, using a crossed-molecular-beam experiment in which individual rotational quantum states of specific conformers of a molecule are separated, we study the chemi-ionization reaction of hydroquinone with metastable neon atoms. We show that collision-induced alignment of the reaction partners caused by geometry-dependent long-range forces influences reaction pathways, which is, however, countered by molecular rotation. The present work provides insights into the conformation-specific stereodynamics of complex polyatomic systems and illustrates the capability of advanced molecule-control techniques to unravel these effects.

Intermolecular interactions and the weakly bound precursor states of elementary physicochemical processes

This study concerns the importance of the precursor (or pre-reactive) state of elementary physicochemical processes whose basic features, as structure, stability, and trapping effect of reagents, are controlled by the balance of intermolecular forces that arise at long range and operate at intermediate and short separation distances. The detailed formulation of such forces, determining formation probability and dynamical evolution of the precursor state, is of relevance in molecular science and difficult to be treated by quantum chemistry. Such a problem has been tackled by us exploiting the phenomenological approach, which employs semi-empirical and empirical formulas to represent strength, range and angular dependence of the leading interaction components involved. In addition to the study of transport phenomena, part of the attention is addressed to chemi-ionization (or Penning ionization) reactions for which neutral reagents lead to atomic and/or molecular ions plus electrons as products. Chemi-ionizations are bimolecular processes occurring in several environments of interest, where a reagent is a species, formed in excited-metastable electronic states by collisions with energetic electrons or cosmic rays. For such reactions all crucial electronic rearrangements, affecting stability and evolution of the weakly bound precursor state, here coincident with the reaction transition state, are characterized with a high detail. The results of the present study are of interest for many other processes, whose precursor states and their relevant features are difficult to characterize, often masked by several other effects.Graphical abstract

Ion-molecule studies of energetic oxygen allotropes in flow tubes: .

Starting in the 1960s, flow tube apparatuses have played a central role in the study of ion-molecule kinetics, allowing for immense chemical diversity of cationic, anionic, and neutral reactants. Here, we review studies of oxygen allotropes, excluding ground state O2 ( ), and focusing instead on reactions of cations, anions, and metal chemi-ionization reactions with ground state atomic oxygen (O 3 P), vibrationally excited molecular oxygen (O2 (v)), electronically excited molecular oxygen (O2 ( )), and ozone (O3 ). Historical outlines of work over several decades are given along with a focus on more recent work by our group at the Air Force Research Laboratory.

Quasi-Static Lineshape Theory for Rydberg Excitations in High-Density Media

This work presents a theoretical approach for lineshapes of Rydberg excitations in high-density media. In particular, we introduce the quasi-static lineshape theory, leading to a methodic and general approach, and its validity is studied. Next, using 84Sr as a prototypical scenario, we discuss the role of the thermal atoms and core–perturber interactions, generally disregarded in Rydberg physics. Finally, we present a characterization of the role of Rydberg–core perturber interactions based on the density and principal quantum number that, beyond affecting the lineshape, could potentially apply to chemi-ionization reactions responsible for the decay of Rydberg atoms in high-density media.

Direct numerical simulation of a turbulent methane/air flame impinged by a sub-breakdown electric field

The effects of an external electric field on a turbulent methane/air diffusion flame are analyzed in this work using direct numerical simulations. The analyzed configuration consists of a temporally evolving mixing layer of air and a mixture of methane and nitrogen at 1 atm that is impinged by an electric field in the direction normal to the mean mixing plane. The combustion and chemi-ionization reactions involved in the flow are modeled using finite-rate chemistry and a reduced reaction scheme consisting of 26 species and 134 reactions. The mass diffusion and ion-wind effects are modeled using a detailed description of the diffusion coefficients and electric mobilities based on kinetic theory. The presented calculations show that the turbulence generated within the mixing layer is mostly unaffected by the applied electric field for the configuration under exam. In fact, the electric body force is developed away from the mixing region where the flow is uniform. Conversely, the turbulence is able to introduce very high intermittency in the electrically charged species concentration and, consequently, in the electric body force. Such intermittency will constitute a challenge in the future formulation of combustion models that take into account ion-wind effects.

The selective role of the orbital angular momentum on the reaction stereo-dynamics

This paper reports on the characterization of the stereo-dynamic controlling three different chemi-ionization reactions, recent objective of our study, since they participate to the balance of phenomena occurring in plasma, interstellar medium, planetary atmospheres, flames and lasers. The optical potential, obtained by a phenomenological method and defined in the whole space of the relative configurations of reagents, has been formulated in an accurate and internally consistent way for three different systems. Some cuts of the multidimensional potential, that asymptotically correlate with a specific fine level of the open shell atom and/or with a defined orientation of the molecular reagent, have been exploited in the present study to emphasize crucial features of the collision dynamics along selected entrance channels of the reactions. Consistently, basic quantities determining the topology of the reaction stereo-dynamics have been properly defined, emphasizing in the three cases relevant changes in the microscopic reaction evolution. Much attention focused on the selectivity of the orbital angular momentum, affecting each collision event at any chosen collision energy. It controls the relative weight of two different reaction mechanisms. The direct reaction mechanism is driven by short-range chemical forces, promoting, by direct electron transfer between reagents, a prototypical elementary oxidation reaction. The indirect mechanism, controlled by the combination of long-range chemical and physical forces, can be triggered by a virtual photon exchanged between reagents, promoting a sort of photo-ionization process. Obtained results and emphasized differences appear to be of general interest for many other elementary processes, more difficult to characterize at this level of detail.Graphic abstract

Electronic Spectroscopy of Jet-Cooled NdO

Chemi-ionization reactions of the type M + O → MO+ + e- (M = Nd or Sm) are currently being investigated as a method to artificially increase the electron density in the ionosphere for control of micro- and radio wave propagation. Experiments involving the release of atomic Nd into the upper atmosphere have resulted in the production of a cloud that, on excitation by solar radiation, emits green light. It has been assumed that NdO was the carrier of this emission, but the existing spectroscopic data needed for this attribution is lacking. While the electronic spectrum of NdO has been well-characterized at wavelengths greater than 590 nm, relatively little spectroscopic data exist for emission wavelengths in the blue-green spectral range. In this study, spectra for jet-cooled NdO were recorded over the range 15,500-21,000 cm-1. Rotationally resolved laser induced fluorescence and vibronically resolved dispersed laser-induced fluorescence spectra were recorded, and nine new electronically excited states were identified. The data indicate that the electronic spectrum of NdO has relatively few allowed transitions in the green spectral range, casting doubt on the assignment of the Nd high-altitude release cloud green emission to NdO.

The topology of the reaction stereo-dynamics in chemi-ionizations

Details on the stereo-dynamic topology of chemi-ionizations highlight the role of the centrifugal barrier of colliding reactants: it acts as a selector of the orbital quantum number effective for reaction in a state-to-state treatment. Here, an accurate internally consistent formulation of the Optical interaction potentials, obtained by the combined analysis of scattering and spectroscopic experimental findings, casts light on structure, energy and angular momentum couplings of the precursor (pre-reactive) state controlling the stereo-dynamics of prototypical chemi-ionization reactions. The closest approach (turning point) of reagents, is found to control the relative weight of two different reaction mechanisms: (i) A direct mechanism stimulated by exchange chemical forces mainly acting at short separation distances and high collision energy; (ii) An indirect mechanism, caused by the combination of weak chemical and physical forces dominant at larger distances, mainly probed at low collision energy, that can be triggered by a virtual photon exchange between reagents.

The role of precursor states in the stereo-dynamics of elementary processes.

The present perspective review focuses on the role of the precursor state, controlling the dynamical evolution of elementary processes, whose structure and stability are often difficult to characterize on quantitative grounds. In particular, such a state depends on the critical balance of weak intermolecular forces operative at long and intermediate separation distances. In this paper, a complementary problem has been properly addressed, concerning the suitable formulation of the intermolecular forces involved, defined in terms of a limited number of parameters and applicable in the whole space of the relative configurations of interacting partners. Important help to the solution of such a problem has been provided by the phenomenological method which adopts semi-empirical and empirical formulas to represent the basic features of the leading interaction components. Such formulas are defined in terms of a few parameters directly or indirectly related to the fundamental physical properties of the interacting partners. In this way, the basic features of the precursor state controlling its stability and its dynamical evolution have been defined in an internally consistent way for several elementary processes, having apparently different natures. Particular attention has been paid to the chemi-ionization reactions: they are treated as prototype oxidation processes for which all electronic rearrangements affecting stability and evolution of the precursor state, coincident with the reaction transition state, have been characterized in great detail. The obtained information appears to be in the perspective of general interest for many other elementary processes, difficult to investigate in the same detail since many other effects mask their basic features.

Guided Ion Beam Studies of the Dy + O → DyO+ + e– Chemi-ionization Reaction Thermochemistry and Dysprosium Oxide, Carbide, Sulfide, Dioxide, and Sulfoxide Cation Bond Energies

Guided ion beam tandem mass spectrometry (GIBMS) was used to measure the kinetic energy dependent product ion cross sections for reactions of the lanthanide metal dysprosium cation (Dy+) with O2, SO2, and CO and reactions of DyO+ with CO, O2, and Xe. DyO+ is formed through an exothermic process when Dy+ reacts with O2, whereas all other processes observed are found to be endothermic. The kinetic energy dependences of these cross sections were analyzed to yield 0 K bond dissociation energies (BDEs) for DyO+, DyC+, DyS+, DyO2+, and DySO+. The 0 K BDE for DyO+ is determined to be 5.60 ± 0.02 eV from the weighted average of six independent thresholds, which are dominated by the slightly endothermic reaction of Dy+ with SO2. Combined with the well-established Dy ionization energy (IE), this value indicates that the chemi-ionization reaction, Dy + O → DyO+ + e-, is endothermic by 0.33 ± 0.02 eV. Theoretical BDEs for Dy+-O, Dy+-C, Dy+-S, ODy+-O, and Dy+-SO were calculated at several levels of theory and basis sets for comparison with experiment with reasonable agreement achieved.

Electronic states and transitions of PrO and PrO+ probed by threshold ionization spectroscopy and spin-orbit multiconfiguration perturbation theory.

The precise ionization energy of praseodymium oxide (PrO) seeded in supersonic molecular beams is measured with mass-analyzed threshold ionization (MATI) spectroscopy. A total of 33 spin-orbit (SO) states of PrO and 23 SO states of PrO+ are predicted by second-order multiconfigurational quasi-degenerate perturbation (MCQDPT2) theory. Electronic transitions from four low-energy SO levels of the neutral molecule to the ground state of the singly charged cation are identified by combining the MATI spectroscopic measurements with the MCQDPT2 calculations. The precise ionization energy is used to reassess the ionization energies and the reaction enthalpies of the Pr+ O → PrO+ + e- chemi-ionization reaction reported in the literature. An empirical formula that uses atomic electronic parameters is proposed to predict the ionization energies of lanthanide monoxides, and the empirical calculations match well with available precise experimental measurements.

Spin-state-controlled chemi-ionization reactions between metastable helium atoms and ground-state lithium atoms.

We demonstrate the control of 4He(23S1)-7Li(22S1/2) chemi-ionization reactions by all-optical electron-spin-state preparation of both atomic species prior to the collision process. Our results demonstrate that chemi-ionization is strongly suppressed (enhanced) for non-spin-conserving (spin-conserving) collisions at thermal energies. These findings are in good agreement with a model based on spin angular momentum coupling of the prepared atomic states to the quasi-molecular states. Small deviations from the model indicate the contribution of the 4Σ+ channel to the reaction rate, which is in violation of spin conservation.

Basic features of Ne*-HX (X = Cl, Br) chemi-ionization reactions.

Total and partial ionization cross sections for Ne*(3P2,0)–HX (X = Cl, Br) are presented in a comparative way as a function of the collision energy between 0.02–0.5 eV. New mass spectrometric data on Ne*–HBr chemi-ionization are discussed and analyzed with already published data on Ne*–HCl, highlighting similarities and differences of the collisional stereodynamics of the two systems. Basic features of the interaction potentials, driving reactive collisions, suggest that reaction channels, leading to the formation of parent HX+ ions in the ground and excited electronic state and to the formation of associated NeHX+ ions as well as of NeH+ proton transfer species, are selectively opened within angular cones exhibiting different orientation and acceptance.

Study of He*/Ne*+Ar, Kr, N2, H2, D2 Chemi-Ionization Reactions by Electron Velocity-Map Imaging.

The chemi-ionization of Ar, Kr, N2, H2, and D2 by Ne(3P2) and of Ar, Kr, and N2 by He(3S1) was studied by electron velocity map imaging (e-VMI) in a crossed molecular beam experiment. A curved magnetic hexapole was used to state-select the metastable species. Collision energies of 60 meV were obtained by individually controlling the beam velocities of both reactants. The chemi-ionization of atoms and molecules can proceed along different channels, among them Penning ionization and associative ionization. The evolution of the reaction is influenced by the internal redistribution of energy, which happens at the first reaction step that involves the emission of an electron. We designed and built an e-VMI spectrometer in order to investigate the electron kinetic energy distribution, which is related to the internal state distribution of the ionic reaction products. The analysis of the electron kinetic energy distributions allows an estimation of the ratio between the two-reaction channel Penning and associative ionization. In the molecular cases the vibrational or electronic excitation enhanced the conversion of internal energy into the translational energy of the forming ions, thus influencing the reaction outcome.

Determination of the SmO+ bond energy by threshold photodissociation of the cryogenically cooled ion.

The SmO+ bond energy has been measured by monitoring the threshold for photodissociation of the cryogenically cooled ion. The action spectrum features a very sharp onset, indicating a bond energy of 5.596 ± 0.004eV. This value, when combined with the literature value of the samarium ionization energy, indicates that the chemi-ionization reaction of atomic Sm with atomic oxygen is endothermic by 0.048 ± 0.004eV, which has important implications on the reactivity of Sm atoms released into the upper atmosphere. The SmO+ ion was prepared by electrospray ionization followed by collisional breakup of two different precursors and characterized by the vibrational spectrum of the He-tagged ion. The UV photodissociation threshold is similar for the 10K bare ion and the He tagged ion, which rules out the possible role of metastable electronically excited states. Reanalysis and remeasurement of previous reaction kinetics experiments that are dependent on D0(SmO+) are included, bringing all experimental results in accord.

Holmium (Ho) oxide, carbide, and dioxide cation bond energies and evaluation of the Ho + O → HoO+ + e- chemi-ionization reaction enthalpy.

Guided ion beam tandem mass spectrometry (GIBMS) and quantum chemical calculations are employed to evaluate the title chemi-ionization reaction with holmium. Exchange reactions of Ho+ with O2, CO, and SO2 and HoO+ with CO, as well as collision-induced dissociation (CID) reactions of HoO+ with Xe, O2, and CO, were performed using GIBMS. Formation of HoO+ is exothermic in reactions with O2 and SO2 but endothermic for reaction with CO, as is the exchange reaction of HoO+ with CO. Quantitative analysis of these reactions and the three CID reactions provides a robust method to determine the bond dissociation energy (BDE) of Ho+-O, 6.02 ± 0.13eV. BDEs for Ho+-C and OHo+-O are also measured as 2.27 ± 0.19 and 2.70 ± 0.27eV, respectively. All three measurements are the first direct determinations of these BDEs. By combining the BDE of HoO+ with the well-established ionization energy of Ho, the exothermicity of Ho in the title chemi-ionization reaction can also be obtained as 0.00 ± 0.13eV. All experimental thermochemistry was then compared to quantum chemical calculations for the purpose of establishing benchmarks and validation. BDEs determined via these calculations are in agreement with the experiment within the inherent experimental and theoretical uncertainties, with results obtained at the coupled-cluster with single, double, and perturbative triple excitations, CCSD(T), using all-electron basis sets yielding the most accurate results.

Stereo-dynamical effects in chemi-ionization reactions of atmospheric O2 and N2 molecules promoted by collisions with Ne*(3P2,0) atoms

This letter focuses on general aspects of the stereodynamics of chemi-ionization reactions, triggered by collisions of O2 and N2 molecules with metastable neon atoms. Basic characteristics of the long-range intermolecular forces involved, some of chemical and others of physical origin, suggest that the weakly bound precursor state, determining the reaction transition state structure and stability, is rather different. Fundamental reaction selectivities are clarified, highlighting differences in the: i) optical potential whose real and imaginary parts must be interdependent; ii) polarizability, quadrupolar moments and orbital representation of the molecules involved, which allow to lay the foundations for future more in-depth investigations.

Chemi-Ionization Reactions and Basic Stereodynamical Effects in Collisions of Atom-Molecule Reagents.

A new theoretical method, developed by our laboratory to describe the microscopic dynamics of gas-phase elementary chemi-ionization reactions, has been applied recently to study prototype atom–atom processes involving reactions between electronically excited metastable Ne*(3P2,0) and heavier noble gas atoms. Important aspects of electronic rearrangement selectivity have been emphasized that suggested the existence of two fundamental microscopic reaction mechanisms. The distinct mechanisms, which are controlled by intermolecular forces of chemical and noncovalent nature respectively, emerge under different conditions, and their balance depends on the collision energy regime investigated. The present paper provides the first step for the extension of the method to cases involving molecules of increasing complexity, whose chemi-ionization reactions are of relevance in several fields of basic and applied researches. The focus is here on the reactions of Ne* with simple inorganic molecules as Cl2 and NH3, and the application of the method discloses relevant features of the reaction microscopic evolution. In particular, this study shows that the balance of two fundamental reaction mechanisms depends not only on the collision energy and on the relative orientation of reagents but also on the orbital angular momentum of each collision complex. The additional insights so emphasized are of general relevance to assess in detail the stereodynamics of many other elementary processes.

Precursor state of chemi-ionization reactions and confinement of valence electrons by anisotropic intermolecular forces

Modifications in atomic alignment and in molecular alignment/orientation determine a different structure of the adduct, formed by collisions of reagents, which represents the precursor state of many elementary chemical–physical processes. The following evolution of the system is directly controlled by the confinement of interacting partners in such a precursor state. However, a deep characterization of these phenomena is still today not fully available, especially when weak intermolecular forces are operative, although the inquiry is of general relevance for the control of the stereodynamics of processes, occurring under a variety of conditions both in gas phase and at surface. In this paper recent advances in the knowledge of the selective role of atomic alignment and molecular orientation effects on the stereodynamics of chemi-ionization reactions will be presented and discussed. These advances represent a basic step along a path whose final target is the complete and internally consistent rationalization and revaluation of the experimental findings already obtained, and published, in our and in other laboratories on chemi-ionization reactions involving as reagent molecules which are of great relevance in several fields. The basic idea is to export important guidelines provided by a recent detailed study of chemi-ionization of noble gas atoms to more complex reactions involving molecules. The main focus of the present paper is on the quantum confinement effects of valence electrons within the reaction transition state.Graphic abstract