projectile charge
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Atoms ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 78
Author(s):  
R. D. DuBois ◽  
O. G. de Lucio

Triply differential data are presented for the 200 eV positron and electron impact ionization of argon. Six electron emission energies between 2.6 and 19 eV, and for scattering angles of 2, 3, and 4 degrees cover a momentum transfer range of 0.16 to 0.31 a.u. The binary and recoil intensities are fitted using a double peak structure in both regions, which, for the present kinematic conditions, are unresolved. The fitted peak intensities and angular positions are shown to have systematic dependences as a function of the momentum transfer and kinematic emission angle, respectively, and illustrate projectile charge effects. A comparison with available theories is made where it is seen that the most notable differences include the fact that for the binary lobe, the observed intensity for emission angles around 100° is absent in the theories, and the theoretical predications overestimate the importance of recoil interactions.


2020 ◽  
Vol 31 (2) ◽  
pp. 45
Author(s):  
Maryam Yahya Al-Abdallah ◽  
Baida M. Ahmed ◽  
Khalid A. Ahmed

The energy losses of ions moving in an electron gas can be studied through the stopping power of the medium. A large number of calculations of the stopping power of ions and electrons in plasmas have been carried out using the random phase approximation (RPA) in the dielectric formalism, for low and high energies. Then we calculated the partial stopping power effective charge (PSPEC) from the energy loss of an incident proton, Ar-ion, and He-ion in target plasma. The Brandt-Kitagawa (BK) model is used to describe the projectile charge fraction (q) and calculate the stopping power and PSPEC, which depends on temperature and electron density ρ(k) of the plasma. This is a topic of relevance to understanding the beam-target interaction in the contexts of particle driven fusion. The presented study is formulated in terms of classical dielectric functions. The programming language Fortran - 90 was used for a required calculation. In the present work, three systems of plasma (Z-pinch, Tokamak, ICF) for different temperatures and densities were covered. Additionally, a comparison has been done with the previous work of plasma.


2019 ◽  
Vol 50 (1) ◽  
pp. 1-16
Author(s):  
S. Halder ◽  
S. Samaddar ◽  
K. Purkait ◽  
M. Purkait

2019 ◽  
Vol 20 (23) ◽  
pp. 6022 ◽  
Author(s):  
Tomasz J. Wasowicz ◽  
Marta Łabuda ◽  
Boguslaw Pranszke

The present work focuses on unraveling the collisional processes leading to the fragmentation of the gas-phase furan molecules under the He+ and He2+ cations impact in the energy range 5–2000 eV. The presence of different mechanisms was identified by the analysis of the optical fragmentation spectra measured using the collision-induced emission spectroscopy (CIES) in conjunction with the ab initio calculations. The measurements of the fragmentation spectra of furan were performed at the different kinetic energies of both cations. In consequence, several excited products were identified by their luminescence. Among them, the emission of helium atoms excited to the 1s4d 1D2, 3D1,2,3 states was recorded. The structure of the furan molecule lacks an He atom. Therefore, observation of its emission lines is spectroscopic evidence of an impact reaction occurring via relocation of the electronic charge between interacting entities. Moreover, the recorded spectra revealed significant variations of relative band intensities of the products along with the change of the projectile charge and its velocity. In particular, at lower velocities of He+, the relative cross-sections of dissociation products have prominent resonance-like maxima. In order to elucidate the experimental results, the calculations have been performed by using a high level of quantum chemistry methods. The calculations showed that in both impact systems two collisional processes preceded fragmentation. The first one is an electron transfer from furan molecules to cations that leads to the neutralization and further excitation of the cations. The second mechanism starts from the formation of the He−C4H4O+/2+ temporary clusters before decomposition, and it is responsible for the appearance of the narrow resonances in the relative cross-section curves.


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