Abstract

The second dissociation channel (CS 2 + → CS + (X 2 Σ) + S( 3 P)) of CS 2 + molecular ions has been investigated by measuring the photofragment CS + excitation (PHOFEX) spectrum in the wavelength range of 385-435 nm, where the CS 2 + molecular ions were prepared purely by [3 + 1] multiphoton ionization of the neutral CS 2 molecules at 483.2 nm. The CS + PHOFEX spectrum was assigned essentially to the CS 2 + (A 2 Π u ) ← CS 2 + (Χ 2 Π g ) transition, such as the S + PHOFEX spectrum, which has been obtained previously. The product branching ratios (CS + /S + ), as measured from the PHOFEX spectra, increase from 0 to slightly larger than 1 in the wavenumber range of 47200-50400 cm - 1 . The adiabatic appearance potential of the CS + ion was determined to be 5.852 ′ 0.005 eV above the Χ 2 Π g , 3 / 2 (0,0,0) level of CS 2 + from the appearance wavenumber of 47196.2 cm - 1 to produce the CS + ion. The dissociation mechanism to get to CS + + S from CS 2 + was discussed and preliminarily attributed to (i) CS 2 + (Χ 2 Π g ) → CS 2 + (A 2 Π u ) through one-photon excitation, (ii) CS 2 + (A 2 Π u ) → CS 2 + (X + ) via internal conversion process due to the vibronic coupling between the A and X states, (iii) CS 2 + (X + ) → CS 2 + (B 2 Σ u +) through the second photon excitation, and (iv) CS 2 + (Β 2 Σ u +) → CS + (X 2 Σ) + S( 3 P), because of the potential curve crossing with the repulsive 4 Σ - state and/or the 2 Σ - state correlated with the second dissociation limit.

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