Muonium depolarization by electron spin exchange with O2 gas in the temperature range 90500 K

Masayoshi Senba, Donald G. Fleming, Donald J. Arseneau, David M. Garner, and Ivan D. Reid
Phys. Rev. A 39, 3871 – Published 1 April 1989
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Abstract

The thermally averaged depolarization cross sections, σ¯D(T), for Mu+O2 electron spin exchange, have been measured by the muon spin relaxation (μSR) technique in a N2 moderator at total pressures near 1 atm over the temperature range 88500 K. These values are related to the thermal spin-flip cross sections of interest (σ¯SF) by a simple numerical factor. At temperatures ≳120 K, σ¯D(T) is essentially temperature independent [with σ¯SF=(5.7±0.5)×1016 cm2], though exhibiting a slight tendency to increase with temperature. At lower temperatures, σ¯SF(T) decreases noticeably. Comparison with the only currently available theoretical calculations of Mu(H)+O2 spin-flip cross sections by Aquilanti, Grossi, and Laganà [Hyperfine Interact. 8, 347 (1981)] on the potential-energy surface of Farantos et al. [Mol. Phys. 34, 947 (1977)] gives poor agreement with the data, particularly in their temperature dependence. The present results for σ¯SF(T) for Mu+O2 qualitatively exhibit the same trend with temperature as found by Desaintfuscien and Audoin [Phys. Rev. A 13, 2070 (1976)] for H-H spin exchange over a comparable temperature range, but the H-H cross sections are, surprisingly, about four times larger. Comparisons with the experimental H+O2 spin-exchange cross sections of Anderle et al. [Phys. Rev. A 23, 34 (1981)] and of Gordon et al. [JETP Lett. 17, 395 (1973)], indicate a significant isotope effect, with σ¯SF(H)1.5σ¯SF(Mu). While this effect can be qualitatively understood in terms of the differing numbers of partial waves involved, detailed theoretical calculations on more recent potential-energy surfaces for HO2 are called for.

  • Received 25 August 1988

DOI:https://doi.org/10.1103/PhysRevA.39.3871

©1989 American Physical Society

Authors & Affiliations

Masayoshi Senba, Donald G. Fleming, Donald J. Arseneau, David M. Garner, and Ivan D. Reid

  • TRIUMF and Department of Chemistry, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Y6

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Vol. 39, Iss. 8 — April 1989

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