Excitation-energy-dependent resonant photoemission: C1s-pi* spectra of carbon monoxide

被引:35
作者
Carravetta, V
Gelmukhanov, FK
Agren, H
Sundin, S
Osborne, SJ
deBrito, AN
Bjorneholm, O
Ausmees, A
Svensson, S
机构
[1] LINKOPING UNIV, IFM, INST PHYS & MEASUREMENT TECHNOL, S-58183 LINKOPING, SWEDEN
[2] UNIV UPPSALA, DEPT PHYS, S-75121 UPPSALA, SWEDEN
[3] UNIV BRASILIA, DEPT PHYS, BR-70910900 BRASILIA, DF, BRAZIL
[4] UNIV COLL GAVLE SANDVIKEN, S-80176 GAVLE, SWEDEN
[5] RUSSIAN ACAD SCI, INST AUTOMAT & ELECTROMETRY, NOVOSIBIRSK 630090, RUSSIA
来源
PHYSICAL REVIEW A | 1997年 / 56卷 / 06期
关键词
D O I
10.1103/PhysRevA.56.4665
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
High-resolution measurements of the x-ray resonant photoemission of CO near the C1s-->pi* transition are presented. The branching ratios for the valence shell ionization close to the resonance how a strong dependence on the photon energy with a clear asymmetry around the resonance energy. It is shown that this energy dependence is due to the presence of the direct photoionization channel in addition to the resonant channel and that it can be theoretically described in the framework of resonant multichannel ionization by a Fano approach. From this general formulation two models, including or excluding the interference between the direct and resonant processes, are derived and numerically evaluated. The no-interference model can explain only the gross features of the measured branching ratios, while inclusion of interference terms in the model can reproduce. almost quantitatively, the experimental results and justifies the observed asymmetry of the branching ratios. It is also proved that the lifetime vibrational interference is absent in the cross section integrated over the photoelectron energy. [S1050-2947(97)01412-1].
引用
收藏
页码:4665 / 4674
页数:10
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