Water dissociation on oxides is of great interest because its fundamental aspects are still not well understood and it has implications in many processes, from ferroelectric polarization screening phenomena to surface catalysis and surface chemistry on oxides. In situ water dissociation and redox processes on metal oxide perovskites which easily expose TiO-terminated surfaces, such as SrTiO, BaTiO or Pb(Zr,Ti)O, are studied by ambient pressure XPS, as a function of water vapour pressure. From the analysis of the O1s spectrum, we determine the presence of different types of oxygen based species, from hydroxyl groups, either bound to Ti and metal sites or lattice oxygen, to different peroxide compounds, and propose a model for the adsorbate layer composition, valid for environmental conditions. From the XPS analysis, we describe the existing surface redox reactions for metal oxide perovskites, occurring at different water vapour pressures. Among them, peroxide species resulting from surface oxidative reactions are correlated with the presence of Ti ions, which are observed to specifically promote surface oxidation and water dissociation as compared to other metals. Finally, surface peroxidation is enhanced by X-ray beam irradiation, leading to a higher coverage of peroxide species after beam overexposure and by ferroelectric polarization, demonstrating the enhancement of the reactivity of the surfaces of ferroelectric materials due to the effect of internal electric fields.
English
Ambient pressure xps; Ambient-pressure x-ray photoelectron spectroscopies; Environmental conditions; Ferroelectric polarization; Ferroelectric surfaces; Internal electric fields; TiO2-terminated surfaces; Water vapour pressure
Ministerio de Economía y Competitividad MAT2016-77852-C2-1-R
Ministerio de Economía y Competitividad FIS2015-73932-JIN
Ministerio de Economía y Competitividad SEV-2015-0496
Ministerio de Economía y Competitividad SEV-2013-0295
Agència de Gestió d'Ajuts Universitaris i de Recerca 2017/SGR-668
Agència de Gestió d'Ajuts Universitaris i de Recerca 2017/SGR-579
Physical chemistry chemical physics ; Vol. 21, issue 9 (March 2019), p. 4920-4930
open access
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