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

Citation
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
Citations number
40
Categorie Soggetti
Physics, Atomic, Molecular & Chemical
ISSN journal
00219606
Volume
98
Issue
12
Year of publication
1993
Pages
9513 - 9522
Database
ISI
SICI code
0021-9606(1993)98:12<9513:ANDIAM>2.0.ZU;2-4
Abstract
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).