Rethinking the molecular structures of WVIOx sites dispersed on titania: distinct mono-oxo configurations at 430 °C and temperature-dependent transformations

Theocharis Kentri; Antonios Trimpalis; Adam Misa; Eleana Kordouli; Theodora Ramantani; Soghomon Boghosian

doi:10.1039/d2dt00595f

Rethinking the molecular structures of W^VIO_x sites dispersed on titania: distinct mono-oxo configurations at 430 °C and temperature-dependent transformations

Dalton Trans. 2022 May 17;51(19):7455-7475. doi: 10.1039/d2dt00595f.

Authors

Theocharis Kentri^{1

2}, Antonios Trimpalis¹, Adam Misa¹, Eleana Kordouli³, Theodora Ramantani¹, Soghomon Boghosian^{1

2

4}

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 Department of Chemistry, University of Patras, Patras, Greece.
⁴ School of Science and Technology, Hellenic Open University, GR-26335 Patras, Greece.

PMID: 35466984
DOI: 10.1039/d2dt00595f

Abstract

The structural properties of the (WO_x)_n phase dispersed on TiO₂ (P25, anatase) at surface densities of 0.5-4.5 W nm^-2 (i.e. up to approximately a monolayer) were explored by using in situ Raman and FTIR spectroscopy, in situ Raman/¹⁸O exchange and Raman spectroscopy in static equilibrium at temperatures of 175-430 °C. Deciphering the temperature and coverage dependence of the spectral features under oxidative dehydration conditions showed that (i) the (WO_x)_n dispersed phase is heterogeneous at 430 °C consisting of two distinct mono-oxo species: Species-I with C_3v-like OW(-O-)₃ configuration (WO mode at 1009-1014 cm^-1) and Species-II with C_4v-like OW(-O-)₄ configuration (WO mode at 1003-1009 cm^-1); (ii) the OW(-O-)₃ site is formed with first order of priority and its formation ceases after the complete consumption of the most basic hydroxyls that are titrated first, hence is abundant at low coverage (<1.5 W nm^-2); (iii) the OW(-O-)₄ site prevails over the OW(-O-)₃ site at medium to high coverage (≥2 W nm^-2) and partially occurs in associated (polymerized) coverages above 2 W nm^-2; (iv) lowering the temperature in the 430 → 250 → 175 °C sequence does not affect the structural and vibrational properties of OW(-O-)₃ but leads to the gradual transformation of the OW(-O-)₄ site to a di-oxo (O)₂W(-O-)₃ site (with a symmetric stretching mode at ∼985 cm^-1) and the partial association of adjacent OW(-O-)₄ units. All temperature-dependent structural/configurational transformations are fully reversible in the 430-175 °C range and are interpreted at the molecular level by a mechanism involving water molecules retained at the surface that act in a reversible temperature-dependent mediative manner resulting in hydroxylation (upon cooling, e.g. to 250 °C) and dehydroxylation (upon heating, e.g. to 430 °C). The Raman spectra obtained for the hydroxyl region confirm the successive hydroxylation/dehydroxylation steps during temperature cycles (e.g. 430 → 250 → 430 °C). One can tune the speciation of the dispersed (WO_x)_n phase under dehydrated conditions by appropriate control of temperature and coverage.