A NEW DIRECT INFRARED-LASER ABSORPTION METHOD FOR STATE-TO-STATE ROTATIONAL ENERGY-TRANSFER IN CROSSED SUPERSONIC JETS - EXPERIMENTAL RESULTS AND QUANTUM SCATTERING ANALYSIS FOR AR+CH4
Dj. Nesbitt et al., A NEW DIRECT INFRARED-LASER ABSORPTION METHOD FOR STATE-TO-STATE ROTATIONAL ENERGY-TRANSFER IN CROSSED SUPERSONIC JETS - EXPERIMENTAL RESULTS AND QUANTUM SCATTERING ANALYSIS FOR AR+CH4, The Journal of chemical physics, 98(12), 1993, pp. 9513-9522
A new method for measuring state-to-state rotational energy transfer i
n crossed supersonic beams is described. The method is based on direct
absorption of tunable, high-resolution infrared laser light by target
molecules collisionally excited into final rotational states. The dir
ect IR absorption approach offers high sensitivity, full quantum state
resolution, a Doppler probe of final velocity components, and is appl
icable to any target molecule that absorbs in the near IR. Preliminary
results are presented for Ar + CH4 scattering in crossed supersonic b
eams at a mean center-of-mass collision energy of 41 meV. Because of t
he high spectral resolution, the method can readily distinguish rotati
onal fine structure states of A, F, and E symmetry in the tetrahedral
group, as well as the much more energetically separated final j states
. The results are compared with full quantum close-coupling calculatio
ns on two different Ar + CH4 potential energy surfaces. The state-to-s
tate scattering results provide a sensitive measure of the potential a
nisotropy, and in particular probe the relative magnitudes of the diff
erent anisotropic terms in the potential (V3 and V4).