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      UPS and UV spectroscopies combined to position the energy levels of TiO 2 anatase and rutile nanopowders

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          Abstract

          Positioning of absolute energy levels and the quantitative description of occupied levels obtained for TiO 2 nanopowders, combining UPS and UV-Vis spectroscopies.

          Abstract

          An accurate experimental determination of electronic structures in semi-conductor nanopowders is a challenging task. We propose here to combine UPS and UV-Vis spectroscopies in order to get the full description of the electronic band alignment of powder samples, TiO 2 rutile and anatase. For UPS measurements, two preparation methods, namely the dropping method and electrophoretic deposition, were used to prepare layers of titania powders on a conducting substrate, ITO or Ag. Both methods lead to comparable results, with a quantitative description of the energy levels from the valence band. Combining these results with the UV-Vis spectra of the same powders enables the determination of the absolute position of the valence band maximum and the conduction band minimum. Combined UPS-UV-Vis spectroscopy provides a better insight into the properties of a powdered material which can differ from single crystal model systems. It can also be used to predict the electronic transfer in mixed phase systems during photocatalytic processes.

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          Journal
          PPCPFQ
          Physical Chemistry Chemical Physics
          Phys. Chem. Chem. Phys.
          Royal Society of Chemistry (RSC)
          1463-9076
          1463-9084
          October 17 2018
          2018
          : 20
          : 40
          : 25629-25637
          Affiliations
          [1 ]Université de Lyon
          [2 ]Institut de Recherches sur la Catalyse et l'Environnement de Lyon – IRCELYON – UMR 5256
          [3 ]CNRS-UCB Lyon 1
          [4 ]69626 Villeurbanne cedex
          [5 ]France
          Article
          10.1039/C8CP04614J
          30288538
          d8959a41-5559-405f-bcf6-dbbc49a23251
          © 2018

          http://rsc.li/journals-terms-of-use

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