Formation ofH(n=2)atoms by the nearly resonant processH+in Cs. Multiple collision processes

Abstract
Formation of H atoms in the n=2 states for the nearly resonant charge-transfer process H+ + Cs (energy defect: 0.49 eV) is studied in the energy range 0.25-3.0 keV. The outgoing H(2S) atoms are quenched in a transverse electric field. The cross section for formation of H(2S) atoms exhibits typical nearly resonant characteristics. The principal maximum, (6.0 ± 0.25) × 1015 cm2 occurs at 0.5-keV H+ energy; a secondary maximum is observed at 1.35 keV. Structure is discussed in terms of the potential-energy curves of the quasimolecule (CsH)+. The cross section for formation of H(2P) atoms is obtained by an indirect method. The H(2S) fraction f relative to the outgoing neutral beam for a thin Cs target is obtained; f is close to the statistical value of 0.25 for H+ energies greater than 1 keV, and has a maximum value of 0.55 ± 0.075 at 0.6 keV. Multiple collisions are studied for Cs targets of variable thickness. The H(2S) fractional yield Fm relative to the total outgoing beam has a maximum for a Cs target thickness of about 1014 atoms/cm2. The largest value of Fm is 0.30 at 0.5 keV. Fm approaches zero as an equilibrium value. A four-component charge-exchange model is used to show that the primary destruction mechanism of H(2S) atoms is collisional deexcitation, with a cross section of about 5 × 1015 cm2. The influence of scattering and calibration of a secondary-emission neutral detector are discussed. Finally, the polarization P of Lyman-α radiation from quenching of H(2S) atoms in a transverse electric field is measured as a function of applied electric field. P is negative, varying from -0.31 ± 0.03 in a near-zero electric field to -0.50 ± 0.06 for a field of 475 V/cm. Data are in agreement with an adiabatic theory; in addition, oscillations about the theoretical curve are observed.