1994
DOI: 10.1063/1.468350
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Auger electron–ion coincidence experiment on nitrogen molecule excited by electron impact

Abstract: The first Auger electron–ion coincidence experiment on the nitrogen molecule excited by electron impact is described. The kinetic energy releases of the N++ and the N+ fragments in the 43–72 eV binding energy range have been measured. The experimental results are compared with previous experimental data obtained by using synchrotron radiation and theoretical predictions.

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Cited by 12 publications
(8 citation statements)
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“…In fact, the N 2+ fragments that originated from process (5) given in table 1 are expected to have low kinetic energy, as we observe in our experiment; this is because the B.E. of the initial + N 2 2 dissociative states (55 eV-68 eV) are very close to the E th =53.9 eV of that process [12,18]. The low intensity of the peaks in this region of the spectra coupled with our poor energy resolution prohibits any quantitative assignment of the configuration of the fragmentation products from our data.…”
supporting
confidence: 52%
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“…In fact, the N 2+ fragments that originated from process (5) given in table 1 are expected to have low kinetic energy, as we observe in our experiment; this is because the B.E. of the initial + N 2 2 dissociative states (55 eV-68 eV) are very close to the E th =53.9 eV of that process [12,18]. The low intensity of the peaks in this region of the spectra coupled with our poor energy resolution prohibits any quantitative assignment of the configuration of the fragmentation products from our data.…”
supporting
confidence: 52%
“…With such an intrinsic energy resolution, the presence of a DC field applied in the interaction region neither produces an appreciable change in the energy resolution of the electrons measured by the CMA nor affects the shape and intensity of the electron energy spectra. The KER values of the fragment ions for the dissociation pathways can be estimated using the relation [18]:…”
Section: Methodsmentioning
confidence: 99%
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“…One way to approach this ''state to state'' photochemistry is to perform coincidence experiments between energy analyzed electrons and fragment ions, as has been recently developed. [7][8][9][10][11][12] However, such experiments remain very difficult, especially in the field of molecules for the following reasons:…”
Section: Introductionmentioning
confidence: 99%