Quantitative assessment of the charge transfer phenomena in cobalt oxides and cobalt complexes is essential for the design of advanced catalytic materials. We propose a method for the evaluation of the oxidation state of cobalt oxides with mixed valence states using resonant photoemission spectroscopy. The method is based on the calculation of the resonant enhancement ratio (RER) from the heights of the resonant features associated with the Co3+ and Co2+ states. The nature of the corresponding states was corroborated by means of density functional calculations. We employed a well-ordered Co3O4(111) film to calibrate the RER with respect to the atomic Co3+/Co2+ ratio. The method was applied to monitor the reduction of a well-ordered Co3O4(111) film to CoO(111) upon annealing under exposure to isopropanol. We demonstrate that this method yields the stoichiometry of cobalt oxides at a level of accuracy that cannot be achieved when fitting the Co 2p core level spectra.

Quantitative Analysis of the Oxidation State of Cobalt Oxides by Resonant Photoemission Spectroscopy

Piccinin S;Farnesi Camellone M;Fabris S;
2019

Abstract

Quantitative assessment of the charge transfer phenomena in cobalt oxides and cobalt complexes is essential for the design of advanced catalytic materials. We propose a method for the evaluation of the oxidation state of cobalt oxides with mixed valence states using resonant photoemission spectroscopy. The method is based on the calculation of the resonant enhancement ratio (RER) from the heights of the resonant features associated with the Co3+ and Co2+ states. The nature of the corresponding states was corroborated by means of density functional calculations. We employed a well-ordered Co3O4(111) film to calibrate the RER with respect to the atomic Co3+/Co2+ ratio. The method was applied to monitor the reduction of a well-ordered Co3O4(111) film to CoO(111) upon annealing under exposure to isopropanol. We demonstrate that this method yields the stoichiometry of cobalt oxides at a level of accuracy that cannot be achieved when fitting the Co 2p core level spectra.
2019
Istituto Officina dei Materiali - IOM -
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/406432
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