Ellis-Gibbings Lilian K, Fortune William G, Cooper Bridgette, Tennyson Jonathan, Price Stephen D
Department of Chemistry, University College London, London WC1H 0AJ, UK.
Phys Chem Chem Phys. 2021 May 21;23(19):11424-11437. doi: 10.1039/d1cp01328a. Epub 2021 May 5.
Absolute partial electron ionisation cross sections, and precursor-specific partial electron ionisation cross sections, for the formation of cations from phosphorus trifluoride (PF) 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 PF 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 PF 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 PF + F, is clearly identified as the lowest triplet state of PF and five different dications (PF, PF, PF, P and F) 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 PF in energetic environments. A first investigation of the bimolecular reactivity of metastable states of PF is also reported. In collisions with Ar, O 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 PF collisions with Ar, and experimental and computational considerations indicate this new chemical bond is formed via a collision complex.
报道了在50 - 200 eV电子能量范围内,三氟化磷(PF₃)形成阳离子的绝对部分电子电离截面以及前体特异性部分电子电离截面。通过使用二维离子 - 离子符合飞行时间质谱测量相对于PF₃形成的截面,并随后使用总电离截面的二元碰撞 - 贝特计算进行缩放来确定绝对值。这个新数据集显著增加了文献中PF₃电子电离的部分电离截面,解决了先前产物离子分支比的差异,并提供了前体特异性截面的首个值。与文献中计算的截面进行比较结果令人鼓舞,尽管个别离子存在差异。符合实验表明,在200 eV电子能量下,双电离和三电离产生约20%的阳离子电离产物。一个解离双阳离子态,解离为PF₂⁺ + F⁺,被明确鉴定为PF₃的最低三重态,并且在质谱中检测到五种不同的双阳离子(PF₂⁺、PF⁺、PF⁺、P²⁺和F⁺)。实验揭示的双阳离子能量学得到了双阳离子电子结构计算研究的支持。所报道的截面将允许更准确地模拟PF₃电离在高能环境中的作用。还报道了对PF₃亚稳态双分子反应性的首次研究。在与Ar、O₂和CO的碰撞中,解离单电子转移主导产物离子产率,而与Ne碰撞后,双阳离子的碰撞诱导解离很重要。对这些过程能量学的考虑表明,反应物双阳离子束包含基态单重态和第一激发三重态的离子。关于三重态寿命的推断得到了符合光谱中亚稳态信号的支持。在PF₃与Ar碰撞后检测到对应于ArF形成的微弱信号,实验和计算考虑表明这种新化学键是通过碰撞复合物形成的。