Ionization and fragmentation of fullerenes in ion collisions with them at various impact parameters

This paper reports on the first measurements of the differential cross sections (with respect to scattering angle) of various elementary processes accompanying electron capture by keV-range H⁺ and He²⁺ ions from a fullerene molecule. Estimation of the impact parameter from the ion scattering angle in the polarization interaction with a fullerene molecule shows that the processes of capture and capture with fullerene ionization and fragmentation occur primarily at impact parameters far exceeding the fullerene radius.     

Elementary processes during collisions of ions with tryptophan molecules

The relative cross sections of elementary processes occurring in single collisions of tryptophan molecules in the gaseous phase with He²⁺ ions with energy 4 keV/u are measured using time-of-flight mass spectrometry for studying the mechanism of radiation damage of amino acid molecules. The fragmentation channels for intermediate singly and doubly charged tryptophan molecular ions formed during one-electron capture, two-electron capture, and electron capture with ionization are investigated. Significant difference is observed in the mass spectra of fragmentation of intermediate doubly charged ions formed during the capture with ionization and double capture, which is associated with different energies of excitation of {C₁₁H₁₂N₂O₂}²⁺* ions.     

Interaction of <Superscript>3</Superscript>He<Superscript>2+</Superscript> and Ar<Superscript>6+</Superscript> ions with acetylene,ethylene, and ethane molecules

Time-of-flight mass spectroscopy methods are employed for studying processes occurring during capture of electrons by ³He²⁺ and Ar⁶⁺ multiply charged ions with energy 6z keV (z is the ion charge) from C₂H _n molecules (n = 2, 4, 6) with different multiplicities of C-C bonds. Fragmentation schemes of the molecular ions formed in such processes are established from analysis of correlations of recording times for all fragment ions. The absolute values of the cross sections of capture of an electron and capture with ionization are measured, as well as the cross sections of formation of fragment ions in these processes. The absolute values of total capture cross sections for several electrons are determined.     

Dissociation of alkane ionized molecules

The subject of investigation is the fragmentation of variously charged molecular ions arising in col-lisions of several kiloelectronvolt H⁺, He²⁺, and Ar⁶⁺ ions with molecules of the simplest alkanes (from methane to butane). Using the method of time-of-flight mass spectrometry, the formation cross sections of dissociation-induced fragment ions are measured. The dissociation takes place when an incident ion captures an electron from a methane, ethane, or propane molecule. The role of additional ionization of the molecule, which accompanies the electron capture by the incident ion, is elucidated. The kinetic energy spectrum for protons resulting from the fragmentation of multiply charged alkane ions is determined. The most plausible kinetic energies of protons depending on the degree of ionization and molecule size fall into the range 1–25 eV. It is shown that, when the molecule loses several electrons, the kinetic energies of protons are governed by Coulomb interaction between all fragment ions and are determined by their flying apart from the relative spatial arrangement of corresponding atoms in a parent molecule.     

Line emission and alignment effects in state selective electron transfer in He2+-Li(2s, 2pΣ, 2pΠ) collisions

Classical Trajectory Monte-Carlo (CTMC) method has been used to investigate state selective electron capture by He²⁺ ions colliding with Li(2s) and Li(2p) in as well as alignments in the energy range 1-15 keV/amu. He⁺(4l) electron capture, line emission [He II(n = 4 3)] cross-sections and alignment parameters have been calculated and analyzed in the light of the available results. The undulatory structure of the capture and emission cross-sections have been explained qualitatively in terms of a quasi-molecular ion formation. Projectile impact energy and spatial overlap play crucial role in determining the alignment effects. Received 3 July 1998 and Received in final form 3 June 1999     

Multiple ionization and fragmentation of the DNA base thymine by interaction with C q+ ions

Ionization and fragmentation of the DNA base thymine upon interaction with keV C^q+ ions (q = 1 - 6) has been studied. By means of time-of-flight spectrometry of two or more thymine fragments in coincidence with an ejected electron we could investigate particular dissociation channels by means of their associated kinetic-energy-release. The fragmentation dynamics are strongly influenced by the C^q+ charge state: for low q values mainly fragmentation due to direct collisions is observed. With increasing q, electron capture becomes more important. For larger q we could identify several Coulomb explosion channels, leading to very energetic fragments.     

Capture of an electron by ions in methionine and norleucine molecules

The relative cross sections of processes taking place when H⁺ and He²⁺ ions with an energy of 6z keV (z is the ionic charge) capture an electron from molecules of C₅H₁₁NO₂S methionine (proteogenic amino acid) and C₆H₁₃NO₂ norleucine (nonproteogenic amino acid) are measured by time-of-flight mass spectrometry (a methionine molecule transforms into a norleucine molecule by substituting the CH₂ group for the S heteroatom). The fragmentation pattern of resulting molecular ions is established from correlation analysis of the detection times of all fragment ions. The results are compared with experimental data for fragmentation of the same molecules ionized by electrons and photons. In these amino acids, the pattern of molecular ion fragmentation is found to depend on the type of molecule ionization. However, the detachment cross section of the COOH neutral group or residue (neutral or charged) R of a side chain of the amino acid is invariably among the largest. The relative cross sections of capture with single and double ionization of molecules are measured.     

Electron Transitions during the Capture of an Electron by a He<Superscript>2+</Superscript> Ion at the Argon Atom

We have measured the absolute values of the total cross section of the one-electron capture by He²⁺ ions in the kinetic energy range 2–30 keV at the Ar atoms. The absolute values of the differential scattering cross sections of He⁺ ions formed during the one-electron capture and the electron capture with ionization at energies of 2.2, 5.4, and 30 keV have been determined. The electronic states of the formed ions have been determined using collision spectroscopy based on analysis of the change in the kinetic energy of He⁺ after the interaction. We have measured doubly differential (with respect to the kinetic energy and the scattering angle) cross sections of the formation of free electrons. The free electron formation channels (direct ionization and electron capture with ionization) have been analyzed by calculating the electron terms of the (HeAr)²⁺ system. The calculated cross section of capture with ionization is in conformity with the cross section measured using collision spectroscopy.     

Recent results on multiple ionization and fragmentation of negatively charged fullerene ions by electron impact

Employing the dynamic crossed-beams technique, the absolute cross sections of the electron-impact multiple ionization and fragmentation of mass-selected negatively charged fullerene ions C _m ^? → C _m?n ²⁺ (m=60, 70, 84; q=1, 2, 3; n=0, 2, 4) were measured. The electron energy varied from the respective threshold up to 1 keV. A scaling law was observed for the cross-section magnitude as a function of the fullerene size m and the charge state q of product ions. The data indicate that different mechanisms account for the detachment of an extra electron from the negatively charged fullerene and the formation of a positively charged ion, respectively. Moreover, the multiple ionization of a fullerene anion is found to be a sequential process. A novel ionization mechanism is proposed which might be expected to be valid for all negatively charged molecular or cluster ions able to shield the attached electron from the incident electron.     

Fragmentation of D- and L-enantiomers of amino acids through interaction with 3He2+ ions

The relative cross section of processes attendant on the capture of an electron by 12-keV ³He²⁺ ions are measured by time-of-flight mass spectrometry for leucine (C₆H₁₃NO₂), methionine (C₅H₁₁NO₂S), and glutmic acid (C₅H₉NO₄) molecules. No differences between the formation relative cross sections of different fragment ions for the D- and L-enantiomeric forms of the amino acids are revealed. The spectrum of glutamic acid fragments taken at temperatures above 110°C is explained by decomposition of the acid with the formation of pyroglutamic acid (C₅H₇NO₃) and water. The results are compared with published data on fragmentation of the same molecules via electron-impact ionization.     

Fragmentation of polyatomic ions produced by electron-loss collisions of butane and isobutane molecules with ions of kiloelectronvolt energy

Fragmentation accompanying the loss of electrons by butane and isobutane (C₄H₁₀) molecules in collisions with energy H⁺, He²⁺, and Ar⁶⁺ ions of kiloelectronvolt energies is studied. The electron density functional technique is applied to C _n H_2n+2 alkane molecules and their respective C _n H _2n+2 ⁺ ions to carry out quantum-chemical calculations of the atomic spacing, electron total energy for the initial configuration of the ionizing molecules and ions in the ground state, and atomic bond breaking energy necessary to produce different ion fragments. The fragmentation energy is correlated with the fragmentation probability. It is shown that the relative cross sections of ion fragmentation depend primarily on the related energy consumption. However, the process cross section is also strongly affected by the initial configuration of C₄H₁₀ isomer molecules, as well as by the amount of dangling and arising atomic bonds involved in the formation of each ion fragment.     

Electron multiplicity in slow collisions of Ar ions with C

Electron capture by Ar⁸⁺ in collisions with C₆₀ fullerene has been investigated using coincident measurements of the number n of ejected electrons, the mass and charge of multicharged Cr+ ₆₀ recoil ions and their fragments Ci+ m and the final charge state of outgoing projectiles Ar(8-s)+ (). The number of captured electrons r is the sum of the numbers of stabilized and emitted electrons: r = n + s. The ratio n / s decreases by a factor three with s increasing from 1 to 7 showing that the multiply excited states populated by capture of a large number of electrons are rather stable against auto-ionisation. Each kinetic energy spectrum of Ar⁺ and Ar²⁺ projectiles is composed of two peaks which we attribute to collisions “inside” and “outside” the C₆₀ cage. The measured energy shift of the projectile keV is consistent with the corresponding energy loss keV in a carbon foil with an equivalent thickness. Inside collisions are characterized by a strong dissociation of recoil ions into light monocharged fragments and by a high multiplicity of ejected electrons. Received: 25 March 1998 / Received in final form and Accepted: 9 June 1998     

Ionisation and fragmentation of tetraphenyl iron (III) porphyrin chloride induced by slow multiply charged ion impact

Ionisation and ion-induced fragmentation of tetraphenyl iron (III) porphyrin chloride (FeTPPCl) molecules have been studied after slow collisions (v∼ 0.2 a.u.) with multiply charged ions (O³⁺, Ar⁸⁺). Intact molecules and large fragments are observed in charge states up to q=4. For q=1, the intact molecule is the most abundant species, in particular, when projectiles in higher charge states are used. When the internal energy of the singly charged ion is increased by the energy transfer during the collision, the singly charged system de-excites by the emission of a neutral Cl-atom, a free electron or possibly a negative Cl anion. The processes are observed as direct as well as delayed processes on a μs-time scale. For q=2 to 4 the loss of the Cl-atom and some phenyl groups becomes more likely due to the lower stability and the larger energy transfer. The charge state distribution of atomic fragments is found to be very different, in particular, when C^q+ and Cl^q+ ions are compared. In the first case mainly singly charged ions are detected, whereas in the second case ions in charge states up to q=6 are observed with high intensities. These phenomena are discussed in terms of the intramolecular charge mobility.     

Fragmentation of adenine and uracyl molecules through electron captures in collisions with ions

The time-of-flight mass spectrometry method is used to study processes occurring when 36-keV multiply charged Ar ions (Ar⁶⁺) capture electrons from adenine and uracyl molecules. Adenine and uracyl constitute one of two base pairs entering into the RNA composition. The fragmentation scheme of resulting molecular ions is derived by analyzing correlations between the detection times of all fragment ions. Fragmentation patterns for molecular ions resulting from molecule ionization by photons, electrons, protons, and multiply charged ions are compared.     

Recombination experiments at CRYRING

Recent advances in studies of electron-ion recombination processes at low relative energies with the electron cooler of the heavy-ion storage ring CRYRING are shown. Through the use of an adiabatically expanded electron beam, collisions down to 10^-4eV relative energies were measured with highly charged ions stored in the ring at around 15 MeV/amu energies. Examples of recombination measurements for bare ions of D⁺, He²⁺, N⁷⁺, Ne¹⁰⁺ and Si¹⁴⁺ are presented. Further on, results of an experiment measuring laser-induced recombination (LIR) into n=3 states of deuterium with polarized laser light are shown. This revised version was published online in July 2006 with corrections to the Cover Date.     

单、双电荷离子与原子碰撞中的激发态和发射截面比较

本文给出了单、双电荷离子和He,Ne,Ar,碰撞过程中产生的激发态的实验结果。He^q+,Ar^q+(q=1,2)离子束实验室能量为(70—170)×q keV。光学测量由光学多道分析系统(OMA)完成,波长范围为200—800nm。观察到单、双电荷离子和原子碰撞中各种不同的激发过程,讨论了发射截面和入射离子电荷数、势能亏损的依赖关系。 关键词：     

H<Superscript>+</Superscript> and He<Superscript>2+</Superscript> impact charge transfer cross sections of magnesium

H⁺ impact single and He²⁺ impact single and double electron capture cross sections of magnesium atoms have been calculated in the modified binary encounter approximation (BEA). The accurate expressions of ion impact s_DE\sigma _{\Delta {E}} (cross section for energy transfer DE\Delta E) and Hartree-Fock momentum distributions of the target electrons have been used throughout the calculations. On the basis of the present work it is concluded that inner shell captures by H⁺ and He²⁺ ions incident on magnesium atoms contribute partly to single electron capture and partly to transfer ionization cross sections. The calculated He²⁺ impact double electron capture cross sections of magnesium are in reasonably good agreement with the experimental observations. This indicates the success of the present theoretical approach in study of charge transfer cross sections of atoms as indirect mechanisms do not interfere with double electron capture processes in this case.     

Branching ratios of successive emission (up to three) of C2n + (n = 1–5) fragments in asymmetrical fission processes of C60 r+ ions (r = 4–6)

Highly charged C₆₀ molecules are produced in collisions between neutral C₆₀ and multiply charged ions within a large range of temperatures. Successive emission of one, two or three light monocharged fragments referred as one-, two- and three-step processes have been observed. The experimental mass branching ratios for the emission of one C_2n⁺ fragment from C₆₀⁶⁺, C₆₀⁵⁺ and C₆₀⁴⁺ ions are compared with the theoretical values using a statistical model. From hotter C₆₀⁶⁺ ions, branching ratios for three-step processes have been measured and the data are in good agreement with an estimation using the branching ratios in one-step process.     

低能He2+-He碰撞体系转移电离机理的实验研究

利用冷靶反冲离子动量谱仪,对低能He²⁺-He碰撞反应中产生的反冲靶离子和炮弹离子进行了符合测量,根据反冲靶离子的动量,研究了转移电离过程中的电荷转移机理.实验结果表明：在20—40 keV能量范围内,靶原子上的一个电子俘获到炮弹离子的基态,另一个电子直接发射到靶的连续态的直接电离及另一个电子俘获到炮弹离子的连续态的过程(ECC)是最主要的转移电离机理,且ECC过程主要发生在大碰撞参数条件下;炮弹离子俘获两个电子处在双激发态的自电离过程的贡献很小. 关键词： 冷靶反冲离子动量谱仪 转移电离机理 离子原子碰撞