Rotational state-resolved differential cross sections (DCS) for spin–multiplet-changing collisions of NO(X 2Π1/2→X 2Π3/2) with Ar are presented and compared to results from previous experimental and theoretical studies performed on the NO/Ar system. A crossed molecular beam apparatus coupled with velocity-mapped ion imaging was used to measure complete (θ=0°–180°) DCS for scattering of NO(X 2Π1/2,j=0.5) into NO(X 2Π3/2,j′) rotational states ranging from j′=1.5 to j′=12.5. Scattered products were detected by state-selective ionization using (1+1′) resonance-enhanced multiphoton ionization via the A 2Σ+ state. State-to-state DCS were extracted in the center-of-mass frame of reference for energy transfer at a center-of-mass collision energy of ∼530 cm−1. Studies performed using horizontally and vertically polarized excitation laser beams yielded DCS which were remarkably similar, indicating that state-to-state scattering for this system is insensitive to probe beam polarization. Experimentally determined angular scattering distributions show primarily forward scattering for low-energy rotational states (j<7.5), with side- and back-scattering increasing with product angular momentum. The scattering results are compared and contrasted to results from earlier experimental investigations and to theoretical results from quantum close-coupling calculations based on ab initio coupled cluster CCSD(T) potential energy surfaces.
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Elioff et al. (2002) studied this question.
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