Ultrafast ionization and fragmentation of molecular silane

被引:20
|
作者
Sayres, Scott G. [1 ]
Ross, Matt W. [1 ]
Castleman, A. W., Jr. [1 ,2 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Phys, University Pk, PA 16802 USA
来源
PHYSICAL REVIEW A | 2010年 / 82卷 / 03期
关键词
FEMTOSECOND LASER INTERACTIONS; COUPLED-CLUSTER SINGLES; KINETIC-ENERGY RELEASE; METHYL-IODIDE CLUSTERS; COULOMB EXPLOSION; MULTIPHOTON IONIZATION; CROSS-SECTIONS; DISSOCIATIVE IONIZATION; PHOTOELECTRON-SPECTRA; MASS-SPECTROMETRY;
D O I
10.1103/PhysRevA.82.033424
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The ionization and fragmentation of molecular silane is examined here with laser intensities ranging between 7 x 10(12) and 1 x 10(15)W/cm(2) at 624 nm. The ionization potential of silane determined using both multiphoton ionization (MPI) and tunneling ionization (TI) models agrees with the vertical ionization potential of the molecule. In addition, the application of the tunneling ionization model is extended here to the fragments of silane to determine their appearance potentials. MPI values for SiH3+, SiH2+, SiH+, Si+, as well as H-2(+) and H+ are consistent with vertical potentials, whereas the TI measurements are found to be in accord with adiabatic potentials. The tunneling appearance potentials observed for the fragments H-2(+) and H+ are lower than reported for other techniques. In fact, the appearance potential measurements for these species resulting from silane are lower than their ionization potentials. The fragmentation rate of silane is determined to be nearly 20 times larger than the ionization rate. The main precursor for producing amorphous silicon (a-Si:H) thin films, SiH3+ is the dominant fragmentation product making up roughly a third of the total ion yield, a substantial increase from other techniques.
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页数:11
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