Full-dimensional theoretical description of vibrationally resolved valence-shell photoionization of H2O

We have performed a full-dimensional theoretical study of vibrationally resolved photoelectron emission from the valence shell of the water molecule by using an extension of the static-exchange density functional theory that accounts for ionization as well as for vibrational motion in the symmetric...

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Detalles Bibliográficos
Autores: Engin, Selma, González Vázquez, Jesús, Maliyar, Gianluigi Grimaldi, Milosavljević, Aleksandar R., Ono, Taishi, Nandi, Saikat, Iablonskyi, Denys, Kooser, Kuno, Bozek, John D., Decleva, Piero, Kukk, Edwin, Ueda, Kiyoshi, Martín García, Fernando
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/715460
Acceso en línea:http://hdl.handle.net/10486/715460
https://dx.doi.org/10.1063/1.5106431
Access Level:acceso abierto
Palabra clave:Synchrotron radiation
photoelectron
kinetic energy
Química
Descripción
Sumario:We have performed a full-dimensional theoretical study of vibrationally resolved photoelectron emission from the valence shell of the water molecule by using an extension of the static-exchange density functional theory that accounts for ionization as well as for vibrational motion in the symmetric stretching, antisymmetric stretching, and bending modes. At variance with previous studies performed in centrosymmetric molecules, where vibrationally resolved spectra are mostly dominated by the symmetric stretching mode, in the present case, all three modes contribute to the calculated spectra, including intermode couplings. We have found that diffraction of the ejected electron by the various atomic centers is barely visible in the ratios between vibrationally resolved photoelectron spectra corresponding to different vibrational states of the remaining H2O+ cation (the so-called v-ratios), in contrast to the prominent oscillations observed in K-shell ionization of centrosymmetric molecules, including those that only contain hydrogen atoms around the central atoms, e.g., CH4. To validate the conclusions of our work, we have carried out synchrotron radiation experiments at the SOLEIL synchrotron and determined photoelectron spectra and v-ratios for H2O in a wide range of photon energies, from threshold up to 150 eV. The agreement with the theoretical predictions is good