Negative ion formation through dissociative electron attachment to the group IV tetrafluorides: Carbon tetrafluoride, silicon tetrafluoride and germanium tetrafluoride

被引:24
|
作者
Bjarnason, E. H. [1 ,2 ]
Omarsson, F. H. [1 ,2 ]
Hoshino, M. [3 ]
Tanaka, H. [3 ]
Brunger, M. J. [4 ,5 ]
Limao-Vieira, P. [3 ,6 ]
Ingolfsson, O. [1 ,2 ]
机构
[1] Univ Iceland, Dept Chem, IS-107 Reykjavik, Iceland
[2] Univ Iceland, Inst Sci, IS-107 Reykjavik, Iceland
[3] Sophia Univ, Dept Phys, Tokyo 1028554, Japan
[4] Flinders Univ S Australia, Sch Chem & Phys Sci, ARC Ctr Antimatter Matter Studies, Adelaide, SA 5001, Australia
[5] Univ Malaya, Inst Math Sci, Kuala Lumpur 5063, Malaysia
[6] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Fis, Lab Colisoes Atom & Mol,CEFITEC, P-2829516 Caparica, Portugal
基金
澳大利亚研究理事会;
关键词
Dissociative electron attachment; Carbon tetrafluoride; Silicon tetrafluoride; Germanium tetrafluoride; SCATTERING CROSS-SECTIONS; LOW-ENERGY ELECTRONS; VIBRATIONAL-EXCITATION; EXCESS ENERGY; IMPACT; CF4; IONIZATION; SPECTROSCOPY; RESONANCES; SIF4;
D O I
10.1016/j.ijms.2013.02.006
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Dissociative electron attachment (DEA) to the group IV tetrafluorides: CF4, SiF4 and GeF4, is reported in the incident electron energy range from about 0 to 14 eV. The F-2(-) formation from CF4 is established and the appearance energies (AEs) for F-, CF3- and F-2(-) are determined using a three-point calibration for the energy scale. These are found to be 4.7 +/- 0.1 eV, 4.5 +/- 0.1 eV and 5.6 +/- 0.1 eV, respectively. For SiF4 the AEs for F-, SiF3- and F-2(-), through the dominating resonance are found to be 10.2 +/- 0.1 eV, 10.2 +/- 0.1 eV and 10.3 +/- 0.1 eV, respectively. From GeF4 the molecular ion GeF4- and the fragments GeF3-, GeF2-, GeF- and F- are all observed with appreciable intensities, and the F- production is found to be significantly close to 0 eV incident electron energy. The present findings are compared with earlier experiments and discussed in context to the thermochemistry of the respective processes as well as the nature of the underlying resonances. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:45 / 53
页数:9
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