期刊
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS
卷 38, 期 11, 页码 R127-R152出版社
IOP PUBLISHING LTD
DOI: 10.1088/0953-4075/38/11/R01
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This paper reviews our recent progress on the angle-resolved photoion-yield spectroscopic (ARPIS) technique applied to the K-shell excitations of the simple linear molecules, N-2, CO, C2H2, O-2, CO2, N(2)6O, OCS and CS2. This spectroscopic technique enables us to distinguish symmetries of electronic states; e.g., the Delta Lambda = 0 parallel and Delta Lambda = 1 perpendicular transitions for the diatomic molecules can be distinguishable. We call this technique symmetry-resolved inner-shell excitation spectroscopy. The complete symmetry resolution is rationalized by the axial-recoil fragmentation. Moreover, the angular distribution of fragment ions is directly related to the molecular orientation upon the photoabsorption and the vibrations; therefore, the ARPIS measurement can be used to reveal complicated vibronic couplings in polyatomic molecules in terms of anisotropy in fragmentation. We have studied Rydberg-valence mixings, vibronically induced 1 s -> Rydberg excited states, and strong bending-mode couplings in Renner-Teller split is -> pi* states for the linear molecules through the ARPIS spectra.
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