Probing the local environment of active sites during 2-propanol oxidation to acetone on the Co3O4 (001) surface: insights from first principles O K-edge XANES spectroscopy

16 November 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

We use theoretical X-ray absorption near-edge spectroscopy (XANES) to investigate the electronic structure of the active sites during 2-propanol oxidation to acetone on the Co3O4 (001) surface in humid conditions. In the gas phase, the O K-edge spectra of 2-propanol and acetone as well that of 2-propoxide considered as reaction intermediate, present no pre-edge peaks. Upon 2-propanol adsorption at the Co site of Co3O4 (001) surface, the O K-edge spectrum presents a distinct peak preceded by a bumb in the pre-edge region, both due to dipole transitions from O 1s to 2p states hybridized with Co 3d empty states. The formation of 2- propoxide leads to two distinct pre-edge peaks due to the increase of 3d empty states. A further increment of these pre-edge peaks is observed when acetone is formed and is rather ascribed to the new contributions of carbon 2p empty states in the transitions occurring in the pre-edge region. The changes observed in the pre-edge peak along the oxidation were correlated to the electronic configuration and hybridization of the cobalt atom directly bonded to alcohol. The variation of electron densities was also monitored for all surface cobalt atoms including the ones on which molecular and dissociated water are adsorbed. The PDOS analysis and crystal field theory showed that adsorption of 2-propanol and molecular water on the surface does not change the oxidation state of +3, while surface cobalt atoms bonded to OH groups have an oxi- dation state of +4. The 3d Loewdin charges analysis shows pronounced cooperative effects between both Co sites during the last oxidation step which corresponds to the decomposition of 2-propoxide to acetone.

Keywords

XANES
pre-edge
oxidation degree
oxidative
Co3O4

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