O_{2}

In CO_{2}-rich atmospheres that are always exposed to ionizing radiation (e.g., Venus and Mars), every fragmentation process can significantly impact the inventory of moieties present in these environments. Nevertheless, the production of O_{2}^{+} ions as a direct result of CO_{2} fragmentation has never been quantified so far. Since molecular oxygen is considered as a potential trace of living organisms, nonbiotic pathways for its production must be known. In this work, O_{2}^{+} coming from CO_{2} fragmentation by electron impact is unambiguously identified and measured in absolute scale.

Three-Body Fragmentation from Single Ionization of Water by Electron Impact: The Role of Satellite States.

Ionization of water with energy transfers close to the 2a1 inner valence orbital is accompanied by a fast electronic rearrangement driven by electron relaxation and electron-electron correlations. Quasi-degenerate single vacancy and satellites one-electron-two-vacancies excited states in outer shells are created and leave their fingerprints in the three-body fragmentation pattern. Single vacancy states have been associated with Auger decay and double ionization. Satellite excited states are here convincingly assigned to single ionization. We focus on the H0 + O+ + H0 fragmentation by electron impact taking advantage of the high sensitivity of the delayed extraction time-of-flight technique to uncover kinematic attributes of suprathermal O+ ions. It is found that the H0 ejections occur under a large angular rearrangement, in an approximate linear geometry, and leaving the O+ near at rest, with ∼50% of the O+ produced in water fragmentation by swift electrons presenting this feature.

A novel double-focusing time-of-flight mass spectrometer for absolute recoil ion cross sections measurements.

In this work, the inclusion of an Einzel-like lens inside the time-of-flight drift tube of a standard mass spectrometer coupled to a gas cell-to study ionization of atoms and molecules by electron impact-is described. Both this lens and a conical collimator are responsible for further focalization of the ions and charged molecular fragments inside the spectrometer, allowing a much better resolution at the time-of-flight spectra, leading to a separation of a single mass-to-charge unit up to 100 a.m.u. The procedure to obtain the overall absolute efficiency of the spectrometer and micro-channel plate detector is also discussed.

Absolute cross sections for O2 dication production by electron impact.

Direct detection of homonuclear diatomic dications using mass spectrometry has the intrinsic inability to distinguish between fragments with the same mass-to-charge ratio, as is the case of the oxygen molecule. In this work, absolute cross sections for the double ionization of the homoisotopic (16)O2 molecule by electron impact, in the 30-400 eV energy range, is reported for the first time, and show significant discrepancies with previous results, obtained with the heteroisotopic (16)O(17)O. The measurements suggest that O2 (++) is mainly produced through post-collisional Auger-like deexcitation.

Ionization and fragmentation of methane induced by 40 eV to 480 eV synchrotron radiation: from valence to beyond core electron ionization.

Photoionization and fragmentation of gaseous methane induced by tunable synchrotron radiation were investigated in a wide energy range, from 40 eV up to 480 eV. We report electron-ion coincidence experiments by measuring the relative partial-ion yields and precursor-specific relative yields for individual fragment ions and for ion fragment pairs as a function of photon energy. The fragmentation patterns are discussed with emphasis on the transition behavior of the bond breaking reactions and of the hydrogen rearrangements from valence to core electron ionization. Below the C 1s threshold, a comparison between photon induced dissociation and electron impact data showed that the ionic fragments formation depends for both projectiles on the same final electronic state reached upon ionization.

Fragmentation and plasmid strand breaks in pure and gold-doped DNA irradiated by beams of fast hydrogen atoms.

The results of an investigation into the damage caused to dry plasmid DNA after irradiation by fast (keV) hydrogen atoms are presented. Agarose gel electrophoresis was used to assess single and double strand break yields as a function of dose in dry DNA samples deposited on a mica substrate. Damage levels were observed to increase with beam energy. Strand break yields demonstrated a considerable dependence on sample structure and the method of sample preparation. Additionally, the effect of high-Z nanoparticles on damage levels was investigated by irradiating DNA samples containing controlled amounts of gold nanoparticles. In contrast to previous (photonic) studies, no enhancement of strand break yields was observed with the particles showing a slight radioprotective effect. A model of DNA damage as a function of dose has been constructed in terms of the probability for the creation of single and double strand breaks, per unit ion flux. This model provides quantitative conclusions about the effects of both gold nanoparticles and the different buffers used in performing the assays and, in addition, infers the proportion of multiply damaged fragments.

Water fragmentation and energy loss by carbon ions at the distal region of the Bragg peak.

Time-of-flight mass spectrometry was used to investigate fragmentation and energy transfer processes in water by C ions at the distal part of the Bragg peak. Measurements of the positive ion fragments from ionization, electron capture, electron loss, transfer-loss and loss-ionization channels have allowed us for the first time (a) to obtain a quantitative determination of the energy lost by C ions in water and (b) to show that total water fragment ion production has a much flatter profile with projectile energy than would be expected if the water radical formation was assumed to follow the energy-loss profile obtained from available stopping power models.

Fragmentation of water by heavy ions.

Absolute cross sections for fragmentation of water molecules by C3+ and O5+ ions over an energy region where the Bragg peak maximizes were measured for ionization, electron capture, and electron loss channels. A collision regime where sigmaSigmaOq+> or =sigmaH2O+ was reached for the first time, producing large abundances of H+ and O+ fragments in comparison to proton impact. Our findings have straightforward implications in the subsequent fast chemistry at the ionization site and on the O production in the first stages of water radiolysis. An unexpected channel-independent relationship between the cross sections for the fragmentation products, which is also approximately independent of the particle type, energy, and charge state, is found. A model is presented to explain such behavior allowing the cross sections of all fragmentation products to be obtained from single and double electron removal cross sections.

Effective strength of the electron-electron interaction in simultaneous projectile and target ionization.

The determination of the right balance between the strong-field interaction of the screened target nucleus and the two-center electron-electron interaction has been controversial since the early attempts to describe the stripping of light, swift ions, by heavy targets. In this work, we find a region of influence for the electron-electron contribution which clearly indicates that this interaction is an essential contribution to the stripping process for both light and heavy targets.