Collision-induced photon emissions (CIE) were observed for keY COt/He collisions from 190 to 1020 nm. The emissions were assigned to the~v = 0 band of the CO;· B 2I: -'> X 2II g electronic transition and the~v = +3, +2, +1,0, -1, -2, -3 vibrational transition progression in the cot A 2II u -'> X zII g electronic transition. The other peaks arise from the emissions of excited 0' fragment atoms and the target gas. The relative intensities of the cot and 0' emissions are independent of the ion translational energy above 3 keY, supporting the curve-crossing mechanism for collisional excitation. Investigation of the relative intensities within the A -n, -'> X 2II g emission of cot indicates that the vibrational distribution is well described by the Franck-Condon [9,10]. This explanation, however, could not explain the similar behavior in the direct excitation process observed in Nt/target collisions [11]. Kelley et aL [8,12] later explained this phenomenon with a more general qualitative curve-crossing model based on the assumption that deviations from vertical transitions during collisions are caused by a short-range, repulsive interaction between the projectile and the target and that these short-range interactions result in the direct translational-vibrational excitation in both the initial and the final electronic states of the diatomic molecule [4, 8,12]. The fact that shortrange forces are involved means that the reaction occurs at small impact parameters. As such, the diatomic molecule cannot be regarded as being isolated. In other words, distortion occurs by chemical forces that are operative in any short-range encounter between two atoms or molecules. Landau and Zener expressed the probability (P) of crossing from one potential curve to another in terms of the slope (dV/dr) difference at the crossing point and the relative velocity (v) of the two colliding species [13,14]. D etection of photon emissions from collisionallyactivated species provides information on the electronic states that are accessible by collisions. This type of emission spectroscopy is often carried out in a mass spectrometer for the study of ion-neutral collisions where the projectile ions collide with a neutral target gas in a collision cell [1][2][3][4][5].Early experiments were carried out to acquire laboratory data on reactions that occur in the earth's atmosphere, in particular on the charge-transfer process. Consistency between experimental results with those predicted by Franck-Condon factors is often used as a sign that electronic transitions in the collision process are vertical [6][7][8]. Moore and Doering have studied the vibrational distribution of the N; B zI: state by observing the relative band intensities of the~v = -1 sequence of the B zI: -'> X zI; emission resulting from the charge-transfer of various projectile atomic/diatomic ions with N z [9]. They concluded that the observed vibrational distributions depend heavily on the laboratory velocity of the reactant ion but very little on its chemical nature. When the velo...