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Glosik, J.; Villinger, H.; Saxer, A.; Richter, R.; Lindinger, W.; Futrell, J.
SASP '84: Symposium on atomic and surface physics1984
SASP '84: Symposium on atomic and surface physics1984
AbstractAbstract
[en] The reaction of N2+ (X,v = o) with H2 is interesting in that the product N2H+ rather than H2+ appears, though the charge transfer to give H2+ (X,v = o) is exoergic by 0.15 eV and a favorable Franck-Condon Factor exists for the H2 (X,v = o) → H2+ (X,v = o) transition (FCF approximately 0.087). Usually charge transfer takes over, when it competes with other reaction mechanisms. However an exception is the charge transfer between Ar+ and N2, where the exoergic channel into N2+ (X,v = o) does not appear at an appreciable rate at thermal and suprathermal energies. The inhibition of this exoergic transfer seems to occur due to nonexistent crossings between the Arsup+ - N2 and N2+ (X,v = o) - Ar potential curves. The same situation may in the case of the N2+ (X,v = o) reaction with H2 inhibit charge transfer, so that heavy particle transfer (hydrogen abstraction) occurs instead. For N2+ (X,v = 1) however a favorable curve crossing seems to allow for a fast charge transfer. (Author)
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Howorka, F.; Lindinger, W.; Maerk, T.D. (eds.); Innsbruck Univ. (Austria). Inst. fuer Atomphysik; 407 p; 1984; p. 132-134; SASP '84: Symposium on atomic and surface physics; Maria Alm (Austria); 29 Jan - 4 Feb 1984
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