Vibrationally Resolved O 1s Photoelectron Spectrum of CO2: Vibronic Coupling and Dynamic Core-Hole Localization

A. Kivimäki, B. Kempgens, K. Maier, H. M. Köppe, M. N. Piancastelli, M. Neeb, and A. M. Bradshaw
Phys. Rev. Lett. 79, 998 – Published 11 August 1997
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Abstract

The C and O 1s photoelectron lines of the CO2 molecule in the gas phase have been measured with vibrational resolution in the threshold region. The vibrational fine structure on the O 1s line is completely dominated by the antisymmetric stretching mode with a frequency of 307 (±3)meV. This mode can be excited only via vibronic coupling, as predicted by Domcke and Cederbaum [Chem. Phys. 25, 189 (1977)], and provides a mechanism for dynamic core-hole localization. Relaxation effects are found to affect strongly the vibrational intensity distribution of the photoelectron line.

  • Received 12 November 1996

DOI:https://doi.org/10.1103/PhysRevLett.79.998

©1997 American Physical Society

Authors & Affiliations

A. Kivimäki, B. Kempgens, K. Maier, H. M. Köppe, M. N. Piancastelli, M. Neeb, and A. M. Bradshaw

  • Fritz-Haber-Institut der Max-Planck-Gesellschaft, Faradayweg 4-6, 14195 Berlin, Germany

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Vol. 79, Iss. 6 — 11 August 1997

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