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Adsorption of formic acid on rutile TiO2 (110) revisited: An infrared reflection-absorption spectroscopy and density functional theory study
Uppsala University, Disciplinary Domain of Science and Technology, Technology, Department of Engineering Sciences, Solid State Physics.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Structural Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Technology, Department of Engineering Sciences, Solid State Physics.
2014 (English)In: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 140, no 3, 034705- p.Article in journal (Refereed) Published
Abstract [en]

Formic acid (HCOOH) adsorption on rutile TiO2 (110) has been studied by s- and p-polarized infrared reflection-absorption spectroscopy (IRRAS) and spin-polarized density functional theory together with Hubbard U contributions (DFT+U) calculations. To compare with IRRAS spectra, the results from the DFT+U calculations were used to simulate IR spectra by employing a three-layer model, where the adsorbate layer was modelled using Lorentz oscillators with calculated dielectric constants. To account for the experimental observations, four possible formate adsorption geometries were calculated, describing both the perfect (110) surface, and surfaces with defects; either O vacancies or hydroxyls. The majority species seen in IRRAS was confirmed to be the bridging bidentate formate species with associated symmetric and asymmetric frequencies of the nu(OCO) modes measured to be at 1359 cm(-1) and 1534 cm(-1), respectively. The in-plane delta(C-H) wagging mode of this species couples to both the tangential and the normal component of the incident p-polarized light, which results in absorption and emission bands at 1374 cm(-1) and 1388 cm(-1). IRRAS spectra measured on surfaces prepared to be either reduced, stoichiometric, or to contain surplus O adatoms, were found to be very similar. By comparisons with computed spectra, it is proposed that in our experiments, formate binds as a minority species to an in-plane Ti-5c atom and a hydroxyl, rather than to O vacancy sites, the latter to a large extent being healed even at our UHV conditions. Excellent agreement between calculated and experimental IRRAS spectra is obtained. The results emphasize the importance of protonation and reactive surface hydroxyls - even under UHV conditions - as reactive sites in e. g., catalytic applications. (C) 2014 AIP Publishing LLC.

Place, publisher, year, edition, pages
2014. Vol. 140, no 3, 034705- p.
National Category
Natural Sciences Engineering and Technology
Research subject
Engineering Science with specialization in Solid State Physics
URN: urn:nbn:se:uu:diva-220815DOI: 10.1063/1.4855176ISI: 000330614400051OAI: diva2:706633
Available from: 2014-03-21 Created: 2014-03-20 Last updated: 2014-07-18Bibliographically approved
In thesis
1. Formic acid adsorption and photodecomposition on rutile TiO2 (110): An in situ infrared reflection absorption spectroscopy study
Open this publication in new window or tab >>Formic acid adsorption and photodecomposition on rutile TiO2 (110): An in situ infrared reflection absorption spectroscopy study
2014 (English)Licentiate thesis, comprehensive summary (Other academic)
Abstract [en]

TiO2 based photocatalysis is an emerging green nanotechnology that can be used forremoval of pollutants from water and air. It has had an increased research interest, bothfrom an application and fundamental point of view, during the last decades. Despite thismany elementary processes that occur on the photocatalyst surface are not fullyunderstood and are thus limiting our ability to purposefully manufacture more efficientphotocatalytic materials.In this licentiate thesis, the adsorption geometry and photodecomposition of formicacid on differently prepared rutile TiO2 (110) surfaces were investigated. The surface wasprepared by repeated cycles of Argon ion sputtering and annealing. By modifying thisprocedure either reduced, stoichiometric or oxylated surfaces have been obtained. Thesedifferent surfaces are all well-ordered as evident from the obtained low energy electrondiffraction pattern. In addition, a totally disordered surface was also prepared by Argonsputtering alone. Grazing incidence infrared reflection-absorption spectroscopy (IRRAS)employing polarized light with different azimuthal orientations of the TiO2 single crystalwas used to investigate the binding geometry of formic acid (HCOOH) on the surface.Upon adsorption of formic acid on the TiO2 surface, the molecule is deprotonatedresulting in a formate (HCOO-) and a hydrogen (H+) molecule on the surface. The formatemolecules are mainly bridge-bonded to the Ti5c surface atoms with their molecular axisalong the [001] direction. A minority of the formate species was found to adsorb throughhydroxylated oxygen vacancies (or protonated oxygen atoms) and therefore have differentorientations on the surface. For the disordered surface, it was found that the orientation ofthe formate adsorbates are more or less random since no changes in the IRRAS spectraare seen for the different directions of the single crystal. The adsorption geometry for thedisordered surface is also changed, as seen in the shift of the peak positions in the IRRASspectra. This changed adsorption geometry is attributed to exposures of Ti3+ atoms on thesurface, and is a result of the Ar ion sputtering.Irradiation of the HCOO/TiO2 systems by UV light (365 nm, 2 mW/cm2) showed onlya small change in formate coverage after 100 minutes of illumination. The decrease waslargest on the disordered surface and miniscule on the ordered surface. These results werecompared with those obtained on rutile nanoparticles at ambient conditions. Thecomparison shows that the adsorption geometry for the nanoparticles is similar to that ofthe ordered single crystal surfaces and that the photodecomposition rate is about a factorof 30 higher on the nanoparticles than on the disordered surface. This difference isexpected as the single crystal experiments were performed in vacuum, where the supplyof O2 electron acceptors and OH/H2O donors from the gas phase is limited.These results shows that the rutile TiO2 (110) surface is a good model system forfundamental studies of nanoparticle systems and that the presence of hydroxylated oxygenvacancies and protonated oxygen atoms are important for the reactivity of the TiO2surface and must be included in the description of surface reactions on rutile surfaces.

Place, publisher, year, edition, pages
Uppsala universitet, 2014. 53 p.
National Category
Condensed Matter Physics
urn:nbn:se:uu:diva-228064 (URN)
2014-06-03, Å4004, The Ångström Laboratory, Lägerhyddsvägen 1, Uppsala, 14:15 (English)
Swedish Research Council, 2010-3514
Available from: 2014-07-15 Created: 2014-07-03 Last updated: 2014-07-15Bibliographically approved

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