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We measure double differential cross sections (DDCS) of electrons emitted from CH4 molecules in collisions with 250 keV protons. The projectile ions are obtained from a 400 kV electron cyclotron resonance-based ion accelerator (ECRIA). We study the energy and angular distributions of the electron DDCS. The observed double and single differential and the total cross section are compared with the state-of-the-art continuum distorted wave eikonal initial state (CDW-EIS) model predictions. Two different approaches are used considering the different target descriptions: complete neglect of differential overlap (CNDO) and molecular orbital (MO) approximations. The MO model uses two different scaling parameters (d = 0.7 and 1.0). In the energy distribution of the DDCS, the carbon KLL Auger line is also observed at 240 eV. The single differential cross section (SDCS) and total cross section (TCS) are derived. Both the MO-based CDW-EIS models are in good agreement with the experimental results; however, the CNDO approach overestimates the data.

We report the development of a supersonic jet assembly to study electron transfer collisions with atoms, molecules, and van der Waals clusters. A comparative study of Ar monomer and dimer cations is presented for different capture-associated channels with a 2.5 keV/u O2+ projectile beam. For the Ar+ + Ar+ fragmentation channel, the interatomic relaxation channels are discussed. The vacancies of the dimer single site or double site show the dependence on capture mechanisms. In the Ar2+ + Ar+ fragmentation channel, double capture, in addition to the single ionization process, dominates. The orientation effect reflects the maximum yield at around 50 and 130 degrees, and angular distributions are nearly symmetric about the axis perpendicular to the dimer axis.

In low energy ion-molecule collisions, electron capture is one of the most important channels. A new experimental setup was developed to study the electron capture process using low-energy ion beams extracted from an electron cyclotron resonance (ECR) plasma-based ion accelerator. Experiments were carried out with the proton beam colliding with water vapor in the energy range of 70–300 keV. Capture events were detected using a position-sensitive detection system comprising micro channel plates (MCPs) and a delay line detector (DLD). These e-capture events can be a result of pure capture reactions as well as transfer ionization. The capture cross section was found to decrease sharply with the beam energy and agreed well with previous measurements. The setup was also used to detect the events that gave rise to the single and multiple e-capture (integrated over all recoil-ion charge states) of C4+ ions. The capture cross-sections for one, two, three, and four electrons were measured for 100 keV C4+ ions. The ratio of multielectron capture yield to that for single e-capture decreased with the number of captured electrons.

Abstract Interaction between polycyclic aromatic hydrocarbon (PAH) molecule and energetic ion is a subject of interest in different areas of modern physics. Here, we present measurements of energy and angular distributions of absolute double differential electron emission cross section for coronene (C24H12) and fluorene (C13H10) molecules under fast bare oxygen ion impact. For coronene, the angular distributions of the low energy electrons are quite different from that of simpler targets like Ne or CH4, which is not the case for fluorene. The behaviour of the higher electron energy distributions for both the targets are similar to that for simple targets. In case of coronene, a clear signature of plasmon resonance is observed in the analysis of forward-backward angular asymmetry of low energy electron emission. For fluorene, such signature is not identified probably due to lower oscillator strength of plasmon compared to the coronene. The theoretical calculation based on the first-order Born approximation with correct boundary conditions (CB1), in general, reproduced the experimental observations qualitatively, for both the molecules, except in the low energy region for coronene, which again indicates the role of collective excitation. Single differential and total cross sections are also deduced. An overall comparative study is presented.

Absolute double differential cross sections (DDCS) of electrons emitted from uracil and 5-bromouracil (BrU) in collisions with protons of energy 200 keV have been measured for various forward and backward emission angles over wide range of electron energies. The measured DDCS are compared with the continuum distorted wave-eikonal initial state (CDW-EIS) calculations. The optimized structure of the BrU was estimated along with the population analysis of all the occupied orbitals using a self-consistent field density. A comparison between the measured DDCS data for the two molecules show that the cross section of low energy electrons emitted from BrU is substantially larger than that for uracil. The BrU-to-uracil DDCS ratios obtained from the present measurements indicate an enhancement of the electron emission by a factor which is as large as 2.0 to 2.5. These electrons being the major agent for damaging the DNA/RNA of the malignant tissues, the present results are expected to provide an important input for the radiosensitization effect in hadron therapy. It is noteworthy to mention that the CDW-EIS calculations for Coulomb ionization cannot predict such enhancement. A large angular asymmetry is observed for uracil with a broad structure, which is absent in case of BrU.