ABSOLUTE STATE-SELECTED TOTAL CROSS-SECTIONS FOR THE ION-MOLECULE REACTIONS O-4,D-2,P-2)+H-2(D-2)((S)
Citation
X. Li et al., ABSOLUTE STATE-SELECTED TOTAL CROSS-SECTIONS FOR THE ION-MOLECULE REACTIONS O-4,D-2,P-2)+H-2(D-2)((S), The Journal of chemical physics, 106(2), 1997, pp. 564-571
Categorie Soggetti
Physics, Atomic, Molecular & Chemical
SICI code
0021-9606(1997)106:2<564:ASTCFT>2.0.ZU;2-5
Abstract
Absolute total cross sections for the state-selected reactions of O+(S
-4,D-2,P-2) + H-2 (D-2) have been measured in the center-of-mass colli
sion energy (E(c.m.)) range of 0.02-12 eV. The cross sections for OH(OD+) from O+(D-2)+H-2(D-2) are slightly higher than those from O+(S-4
)+H-2(D-2), whereas the OH+ (OD+) cross sections from O+ (P-2)+H-2(D-2
) are approximate to 40% lower than those from O+(S-4)+H-2 (D-2) and O
+ (D-2) + H-2 (D-2). At E(c.m.) <0.5 eV, the total cross sections for
OH+ (OD+) from O+ (S-4)+H-2 (D-2) and O+(D-2)+H-2 (D-2) are in accord
with those predicted by the Langevin-Gioumousis-Stevenson model. Signi
ficantly higher cross sections are observed for H+ (D+) and H-2(+) (D-
2(+)) from O+(D-2)+H-2 (D-2) and O+(P-2)+H-2 (D-2), as compared to tho
se from O+(S-4)+H-2 (D-2). The exothermic nature of the O+(D-2, P-2) H-2 (D-2) charge transfer collisions accounts for the high cross sect
ions are identified with the H+ (D+)+O+H channel, the H+ (D+) ions fro
m the reactions involving O+(D-2) and O+(P-2) are associated mostly wi
th the H+ (D+)+OH(OD) channel, the formation of which obeys the spin-c
onservation rule. The comparison of the sum (sigma(T)) of cross sectio
ns for OH+ (OD+), H-2(+) (D-2(+)), and H+ (D+) from O+(S-4)+H-2(D-2) t
o those from O+(D-2)+H-2(D-2) and O+(P-2)+H-2 (D-2) shows that the sig
ma(T)s for O+(S-4)+H-2(D-2), O+(D-2)+H-2(D-2), and O+(P-2)+H-2(D-2) at
E(c.m.) <0.5 eV are comparable. At E(c.m.)>0.5 eV, the sigma(T)s for
O+(P-2)+H-2 (D-2) are greater than those for O+(D-2)+H-2 (D-2), which
in turn are greater than those for O+(S-4)+H-2 (D-2). This observation
is attributed to the increase in the number of accessible product cha
nnels for reactions involving the excited O+(D-2) and O+(P-2) reactant
ions. (C) 1997 American Institute of Physics.