Vibrationally resolved O 1s core-excitation spectra of CO and NO

被引:99
作者
Püttner, R
Dominguez, I
Morgan, TJ
Cisneros, C
Fink, RF
Rotenberg, E
Warwick, T
Domke, M
Kaindl, G
Schlachter, AS
机构
[1] Free Univ Berlin, Inst Phys Expt, D-14195 Berlin, Germany
[2] Lawrence Berkeley Lab, Berkeley, CA 94720 USA
[3] Wesleyan Univ, Dept Phys, Middletown, CT 06459 USA
[4] Inst Fis, Cuernavaca 62191, Morelos, Mexico
[5] Ruhr Univ Bochum, Lehrstuhl Theoret Chem, D-44780 Bochum, Germany
来源
PHYSICAL REVIEW A | 1999年 / 59卷 / 05期
关键词
D O I
10.1103/PhysRevA.59.3415
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
High-resolution photoabsorption spectra of CO and NO below the O is ionization threshold are presented. The vibrational fine structure of the O 1s-->pi* and O 1s(-1) Rydberg excitations could be resolved for both molecules, allowing a determination of the vibrational energies and intramolecular distances of the core-excitation states in CO and NO from Franck-Condon analyses. Ab initio calculations are performed for the O 1s--> pi* excitation in CO to give an independent confirmation of the spectroscopic parameters derived from the Franck-Condon analysis. The spectral features of the O 1s(-1) Rydberg region in CO are reassigned on the basis of the experimental results. The results obtained for the O 1s(-1)3s Rydberg state in NO support the idea of a weakening of the molecular bond upon an O 1s(-1) ionization process. [S1050-2947 (99)06205-8].
引用
收藏
页码:3415 / 3423
页数:9
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