Ionisation of PF3: absolute partial electron ionisation cross sections and the formation and reactivity of dication states. Issue 19 (5th May 2021)

• Record Type: Journal Article
• Authors: Ellis-Gibbings, Lilian K.; Fortune, William G.; Cooper, Bridgette; Tennyson, Jonathan; Price, Stephen D.
• Is Part Of: Physical chemistry chemical physics. Volume 23:Issue 19(2021)
• Page Start: 11424
• Page End: 11437
• Publication Date: 2021-05-05
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/d1cp01328a
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Single and multiple electron ionization of PF3 is characterized and quantified by a joint computational and experimental investigation. Absolute cross sections are presented and the properties of two low-lying dication states revealed. Abstract : Absolute partial electron ionisation cross sections, and precursor-specific partial electron ionisation cross sections, for the formation of cations from phosphorus trifluoride (PF3 ) are reported over the electron energy range 50–200 eV. The absolute values are determined by the measurement of cross sections relative to the formation of PF3 + using 2D ion–ion coincidence time-of-flight mass spectrometry and subsequent scaling using binary encounter-Bethe calculations of the total ionisation cross section. This new dataset significantly augments the partial ionisation cross sections for electron ionization of PF3 found in literature, addressing previous discrepancies in the branching ratios of product ions, and provides the first values for the precursor-specific cross sections. Comparisons to calculated cross sections from the literature are encouraging, although there are discrepancies for individual ions. The coincidence experiments indicate that double and triple ionisation generate approximately 20% of the cationic ionisation products at 200 eV electron energy. One dissociative dication state, dissociating to PF2 + + F +, is clearly identified as the lowest triplet state of PF3 2+ and five different dications (PF3 2+, PF2 2+, PF 2+, P 2+ and F 2+ ) are detected in the mass spectra. The dication energetics revealed by the experiments are supported by a computational investigation of the dication's electronic structure. The cross sections reported will allow more accurate modelling of the role of the ionization of PF3 in energetic environments. A first investigation of the bimolecular reactivity of metastable states of PF3 2+ is also reported. In collisions with Ar, O2 and CO dissociative single electron transfer dominates the product ion yield, whereas collision-induced dissociation of the dication is important following collisions with Ne. Consideration of the energetics of these processes indicates that the reactant dication beam contains ions in both the ground singlet state and the first excited triplet state. The deduction regarding the longevity of the triplet state is supported by metastable signals in the coincidence spectra. Weak signals corresponding to the formation of ArF + are detected following PF3 2+ collisions with Ar, and experimental and computational considerations indicate this new chemical bond is formed via a collision complex.