Heterogeneity of the vanadia phase dispersed on titania. Co-existence of distinct mono-oxo VOx sites

Theocharis Kentri; Athanasios Tsevis; Soghomon Boghosian

doi:10.1039/d3dt00749a

Heterogeneity of the vanadia phase dispersed on titania. Co-existence of distinct mono-oxo VO_x sites

Dalton Trans. 2023 Jun 6;52(22):7495-7511. doi: 10.1039/d3dt00749a.

Authors

Theocharis Kentri^{1

2}, Athanasios Tsevis³, Soghomon Boghosian^{1

2

3}

Affiliations

¹ Department of Chemical Engineering, University of Patras, Patras, Greece. bogosian@chemeng.upatras.gr.
² Institute of Chemical Engineering Sciences, FORTH/ICE-HT, Patras, Greece.
³ School of Science and Technology, Hellenic Open University, GR-26335 Patras, Greece.

PMID: 37211989
DOI: 10.1039/d3dt00749a

Abstract

The structural and configurational characteristics of the species comprising the (VO_x)_n phase dispersed on TiO₂(P25) are studied under oxidative dehydration conditions by in situ molecular vibrational spectroscopy (Raman, FTIR) complemented by in situ Raman/¹⁸O isotope exchange and Raman spectroscopy under static equilibrium at temperatures of 175-430 °C and coverages in the 0.40-5.5 V nm^-2 range. It is found that the dispersed (VO_x)_n phase consists of distinct species with different configurations. At low coverages of 0.40 and 0.74 V nm^-2, isolated (monomeric) species prevail. Two distinct mono-oxo species are found: (i) a majority Species-I, presumably of distorted tetrahedral OV(-O-)₃ configuration with VO mode at 1022-1024 cm^-1 and (ii) a minority Species-II, presumably of distorted octahedral-like OV(-O-)₄ configuration with VO mode at 1013-1014 cm^-1. Cycling the catalysts in the 430 → 250 → 175 → 430 °C sequence results in temperature-dependent structural transformations. With decreasing temperature, a Species-II → Species-I transformation with concomitant surface hydroxylation takes place by means of a hydrolysis mechanism mediated by water molecules retained by the surface. A third species (Species-III, presumably of di-oxo configuration with ν_s/ν_as at ∼995/985 cm^-1) occurs in minority and its presence is increased when further lowering the temperature according to a Species-I → Species-III hydrolysis step. Species-II (OV(-O-)₄) shows the highest reactivity to water. For coverages above 1 V nm^-2, an association of VO_x units takes place leading to gradually larger polymeric domains when the coverage is increased in the 1.1-5.5 V nm^-2 range. Polymeric (VO_x)_n domains comprise building units that maintain the structural characteristics (termination configuration and V coordination number) of Species-I, Species-II, and Species-III. The terminal VO stretching modes are blue-shifted with increasing (VO_x)_n domain size. A lower extent of hydroxylation is evidenced under static equilibrium forced dehydrated conditions, thereby limiting the temperature dependent structural transformations and excluding the possibility of incoming water vapors as the cause for the temperature dependent effects observed in the in situ Raman/FTIR spectra. The results address open issues and offer new insight in the structural studies of VO_x/TiO₂ catalysts.