1994
DOI: 10.1088/0953-4075/27/12/012
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Experimental study of the Penning ionization of the H2O molecule by He* (23S, 21S) metastable atoms

Abstract: Penning ionization of the H a molecule by the He'(2'S) metastable atom is studied. The energy shift is measured for the three observed X, A and B eiectronic bands of the residual HzO' ion. The absence of the vibrational structures is discussed in light of the known interaction potential surface of the He'-t120 complex. More altention is given to the X electronic band characterized by interference structures at high electron energy and an important angular dependence intensity.

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Cited by 10 publications
(5 citation statements)
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References 33 publications
(7 reference statements)
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“…Also in these cases we recorded negative energy shifts having a bigger value, indicating a more attractive behavior in the case of He * -M collisions respect to Ne * -M collisions (with M = H2S, NH3). This observation is in fairly good agreement with previous results obtained by Ohno et al [27] and Ben Arfa et al [39] P2 state), which is the fundamental physical property of the partners, enhancing the attractive interaction behavior of the potential energy surfaces [22]. As already discussed in previous papers [22,23], by a simple analysis of obtained PIES spectra, in the case of H2O + -1b1, H2S + -2b1, and NH3 + shift, εmax, from the change in position of the maximum of peak but also the shift between the electron energy value where the peak intensity drops down to 44% of its maximum at the lower energy side, εA, with respect to the nominal energy, ε0 [40].…”
Section: Resultssupporting
confidence: 94%
“…Also in these cases we recorded negative energy shifts having a bigger value, indicating a more attractive behavior in the case of He * -M collisions respect to Ne * -M collisions (with M = H2S, NH3). This observation is in fairly good agreement with previous results obtained by Ohno et al [27] and Ben Arfa et al [39] P2 state), which is the fundamental physical property of the partners, enhancing the attractive interaction behavior of the potential energy surfaces [22]. As already discussed in previous papers [22,23], by a simple analysis of obtained PIES spectra, in the case of H2O + -1b1, H2S + -2b1, and NH3 + shift, εmax, from the change in position of the maximum of peak but also the shift between the electron energy value where the peak intensity drops down to 44% of its maximum at the lower energy side, εA, with respect to the nominal energy, ε0 [40].…”
Section: Resultssupporting
confidence: 94%
“…The experimental apparatus has been fully described elsewhere by Ben Arfa et al [31]. The metastable projectile beam and the target one are formed by effusion through a multi-capillary array and cross at right angles.…”
Section: Methodsmentioning
confidence: 99%
“…In the excitation transfer process, this is understood to be the result of the long life time of the intermediate Rydberg state allowing the molecule to rotate before autoionization, but in attractive collision systems, the isotropic angular distribution is explained as the effect of the spiralling classical collision trajectory. It is well established that an attractive collision system leads to a broad vibronic band in the electron energy spectrum, as in the case of He * -H 2 O (Cermak 1977, Ben Arfa et al 1994. So the observed non-Franck-Condon vibrational population of the X band and the isotropic angular behaviour of the additional vibrational structures rationalise the hypothesis of the excitation transfer in the He * -CO collision.…”
Section: Resultsmentioning
confidence: 58%