Coupled electron-nuclear dynamics in resonant 1 σ → 2 π x-ray Raman scattering of CO molecules
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2016
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We present a detailed experimental-theoretical analysis of O K-edge resonant 1σ-2π inelastic x-ray scattering
(RIXS) from carbon monoxide with unprecedented energy resolution. We employ high-level ab initio calculations
to compute the potential energy curves of the states involved in the RIXS process and simulate the measured
RIXS spectra using the wave-packet-propagation formalism, including Coulomb coupling in the final-state
manifold. The theoretical analysis allows us to explain all the key features of the experimental spectra, including
some that were not seen before. First, we clearly show the interference effect between different RIXS channels
corresponding to the transition via orthogonal 1
x and 1
y core-excited states of CO. Second, the RIXS
region of 13 eV energy loss presents a triple structure, revealed only by the high-resolution measurement. In
previous studies, this region was attributed solely to a valence state. Here we show a strong Coulomb mixing
of the Rydberg and valence final states, which opens the forbidden RIXS channels to the “dark” final Rydberg
states and drastically changes the RIXS profile. Third, using a combination of high-resolution experiment and
high-level theory, we improve the |4σ −12π1 final-state potential-energy curve by fitting its bottom part with the
experiment. Also, the coupling constants between Rydberg and valence states were refined via comparison with
the experiment. Our results illustrate the large potential of the RIXS technique for advanced studies of highly
excited states of neutral molecules.
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COUTO, Rafael C. et al. Coupled electron-nuclear dynamics in resonant x-ray Raman scattering of CO molecules. Physical Review A, [s. l.], v. 93, n. 3, e032510, 2016. DOI: 10.1103/PhysRevA.93.032510. Disponível em: https://journals.aps.org/pra/abstract/10.1103/PhysRevA.93.032510. Acesso em: 13 dez. 2023.