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dc.contributor.authorTanaka, T.zh_CN
dc.contributor.authorMakochekanwa, C.zh_CN
dc.contributor.authorTanaka, H.zh_CN
dc.contributor.authorKitajima, M.zh_CN
dc.contributor.authorHoshino, M.zh_CN
dc.contributor.authorTamenori, Y.zh_CN
dc.contributor.authorKukk, E.zh_CN
dc.contributor.authorLiu, X. J.zh_CN
dc.contributor.authorPrumper, G.zh_CN
dc.contributor.authorUeda, K.zh_CN
dc.contributor.author刘兴军zh_CN
dc.date.accessioned2013-12-12T02:03:09Z
dc.date.available2013-12-12T02:03:09Z
dc.date.issued2005zh_CN
dc.identifier.citationPhysical Review Letters,95(20):zh_CN
dc.identifier.issn0031-9007zh_CN
dc.identifier.otherISI:000233243500019zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/59102
dc.description.abstractSymmetry-resolved x-ray absorption spectroscopy has been first carried out on high-temperature molecules. From the angle-resolved ion yield spectra of CO2 both at room temperature and at 430 degrees C, symmetry-resolved absorption profiles of the C 1s(-1)2 pi(u) and O 1s(-1)2 pi(u) resonances have been extracted for the vibrational ground state molecules and bending-vibration excited ones. The profiles change dramatically between them, and the Renner-Teller effect becomes more evident for the vibrationally excited molecules. The effects of the multimode vibronic coupling are suggested for the O 1s(-1)2 pi(u) and O 1s(-1)3s sigma(g) resonances.zh_CN
dc.language.isoen_USzh_CN
dc.subjectCOREzh_CN
dc.subjectSTATESzh_CN
dc.titleSymmetry-resolved absorption spectra of vibrationally excited CO2 moleculeszh_CN
dc.typeArticlezh_CN


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