Near-threshold shape resonance in the photoionization of 2-butyne

被引:24
|
作者
Xu, Hong [1 ]
Jacovella, U. [1 ]
Ruscic, B. [1 ]
Pratt, S. T. [1 ]
Lucchese, R. R. [2 ]
机构
[1] Argonne Natl Lab, Argonne, IL 60439 USA
[2] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2012年 / 136卷 / 15期
关键词
IONIZATION CROSS-SECTIONS; HARTREE-FOCK; CONFIGURATION-INTERACTION; PHOTOELECTRON-SPECTRA; BASIS-SETS; ELECTRON; SPECTROSCOPY; SCATTERING; CHEMISTRY; ISOMERS;
D O I
10.1063/1.3701762
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Photoelectron velocity map imaging is combined with one-and two-photon ionization to study the near threshold photoionization of the 2-butyne molecule. In this region, the photoabsorption and photoionization cross sections display a very intense broad feature that is assigned to an l = 4, pi (g) shape resonance. The effect of this shape resonance on the vibrational branching ratios and photoelectron angular distributions is explored. Theoretical calculations of the photoionization cross section and photoelectron angular distributions are in good agreement with the experiments. The results for 2-butyne are compared with those of acetylene, propyne, and 1-butyne, none of which show such significant enhancements near threshold, and the differences are rationalized in terms of the symmetries and orbital angular momenta of the highest occupied orbitals and the corresponding shape resonances. Expectations for larger alkynes and alkynyl radicals are also discussed. A preliminary measurement of the ionization energy of the 2-butyne dimer is also presented. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3701762]
引用
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页数:10
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