Interference Effects in Auger Resonant Raman Spectra of CO via Selective Vibrational Excitations Across the O 1s -2? Resonance
The Auger resonant Raman spectra of CO, arising from the transitions to the X and A final electronic states of CO+, have been recorded at photon energies corresponding to the vibrational excitations v[prime]=3,5, and 8 in the O 1s-->2pi resonance. The spectra are simulated within the model that takes into account both the lifetime-vibrational interference (LVI) and interference with the nonresonan
