Phosphine/silane mixtures have been investigated by ion trap mass spectrometry, and reaction pathways together with rate constants of the main reactions are reported. Mechanisms of ion-molecule reactions have been elucidated by single and multiple isolation steps, and exact mass measurements have been performed by Fourier transform mass spectrometry. The SiHn + (n ) 0-3) ions react with phosphine to give SiPHn + (n ) 1-4) ions. These ions further react and yield SiP2Hn + (n ) 2-5) and Si2PHn + (n ) 3-7) ions, which, in turn, react following different pathways with silane or phosphine to give Si2P2Hn + (n ) 5, 6, 8) and Si3PHn + (n ) 5-7), respectively. Mixed SiPHn + (n ) 1-4) ions also originate from the PHn + (n ) 0, 1) phosphine primary ions, as well as from the P2Hn + (n ) 0-3) secondary ions of phosphine. Protonation of phosphine from several ionic precursors is a very common process and yields the stable phosphonium ion, PH4 +. Trends in total abundances of tertiary SiP2Hn + (n ) 2-4) and Si2PHn + (n ) 3-7) ions as a function of reaction time for different PH3/SiH4 pressure ratios show that excess of silane favors the nucleation of mixed Si-P ions. The mechanism and energetics of the reaction of Si+ with PH3 have been investigated by ab initio calculations, and the most stable structure of the SiPH+ product, with a hydrogen bridge between silicon and phosphorus, has been identified.

Gas Phase Ion-Molecule Reactions in Phosphine/Silane Mixtures

ANTONIOTTI, Paola;OPERTI, Lorenza;RABEZZANA, Roberto;VAGLIO, Gian Angelo;
1996-01-01

Abstract

Phosphine/silane mixtures have been investigated by ion trap mass spectrometry, and reaction pathways together with rate constants of the main reactions are reported. Mechanisms of ion-molecule reactions have been elucidated by single and multiple isolation steps, and exact mass measurements have been performed by Fourier transform mass spectrometry. The SiHn + (n ) 0-3) ions react with phosphine to give SiPHn + (n ) 1-4) ions. These ions further react and yield SiP2Hn + (n ) 2-5) and Si2PHn + (n ) 3-7) ions, which, in turn, react following different pathways with silane or phosphine to give Si2P2Hn + (n ) 5, 6, 8) and Si3PHn + (n ) 5-7), respectively. Mixed SiPHn + (n ) 1-4) ions also originate from the PHn + (n ) 0, 1) phosphine primary ions, as well as from the P2Hn + (n ) 0-3) secondary ions of phosphine. Protonation of phosphine from several ionic precursors is a very common process and yields the stable phosphonium ion, PH4 +. Trends in total abundances of tertiary SiP2Hn + (n ) 2-4) and Si2PHn + (n ) 3-7) ions as a function of reaction time for different PH3/SiH4 pressure ratios show that excess of silane favors the nucleation of mixed Si-P ions. The mechanism and energetics of the reaction of Si+ with PH3 have been investigated by ab initio calculations, and the most stable structure of the SiPH+ product, with a hydrogen bridge between silicon and phosphorus, has been identified.
1996
100
155
162
P. Antoniotti; L. Operti; R. Rabezzana; G.A. Vaglio; P. Volpe; J.-F. Gal; R. Grover; P.-C. Maria
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/107583
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