Abstract
Cross sections, differential in translational energy gain and projectile scattering angle, for single- and double-electron capture processes in collisions of ${\mathrm{C}}^{5+}$ ions with He at laboratory energies between 0.5 and 50 keV/u, have been studied experimentally by means of a high-resolution cold-target recoil-ion momentum spectroscopy. The translational energy spectra for single-electron capture show that capture into the ${\mathrm{C}}^{4+}$ $(n=3)$ state is the dominant reaction channel observed over the entire collision energy region studied, in agreement with close-coupling calculations. However, capture into $n=2$ and $n>~4$ states is only significant at $E>~4 \mathrm{k}\mathrm{e}\mathrm{V}/\mathrm{u}.$ Transfer excitation processes contribute only very weakly to the total cross sections for single-electron capture (2--4 %). This contribution is considerably smaller than the close-coupling prediction. The autoionizing double-electron-capture (transfer ionization) spectrum clearly shows that ${\mathrm{C}}^{3+}$ ${(2l,2l}^{\ensuremath{'}})$ states are populated at the lowest impact energy, whereas contributions from capture into ${\mathrm{C}}^{3+}$ ${(2l,n}^{\ensuremath{'}}{l}^{\ensuremath{'}})$ states with ${n}^{\ensuremath{'}}>~3$ increase as the impact energy is increased and become the dominant process at $E=35 \mathrm{k}\mathrm{e}\mathrm{V}/\mathrm{u}.$ State-selective and differential cross sections have also been measured and compared with the close-coupling and multichannel Landau-Zener calculations.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.