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The Role of Cerium Valence in the Conversion Temperature of H 2 Ti 3 O 7 Nanoribbons to TiO 2 -B and Anatase Nanoribbons, and Further to Rutile

ORCID
0000-0003-1825-9523
Affiliation
Jožef Stefan Institute, Jamova Cesta 39, 1000 Ljubljana, Slovenia;
Umek, Polona;
ORCID
0000-0002-9047-6541
Affiliation
Karlsruhe Institute of Technology, P.O. Box 6980, 706049 Karlsruhe, Germany;
Dürrschnabel, Michael;
Affiliation
Department of Materials and Earth Sciences, Technische Universität Darmstadt, Peter-Grünberg-Strasse 2, 64287 Darmstadt, Germany;
Molina-Luna, Leopoldo;
ORCID
0000-0001-8071-0421
Affiliation
Jožef Stefan Institute, Jamova Cesta 39, 1000 Ljubljana, Slovenia;
Škapin, Srečo;
ORCID
0000-0002-3486-5219
Affiliation
Faculty of Chemistry and Chemical Technology, University of Ljubljana, Večna Pot 113, 1000 Ljubljana, Slovenia;
Korošec, Romana Cerc;
ORCID
0000-0002-3330-6693
Affiliation
Chimie des Interactions Plasma-Surface (ChIPS), Research Institute for Materials Science and Engineering, University of Mons, 7000 Mons, Belgium
Bittencourt, Carla

CeO 2 -TiO 2 is an important mixed oxide due to its catalytic properties, particularly in heterogeneous photocatalysis. This study presents a straightforward method to obtain 1D TiO 2 nanostructures decorated with CeO 2 nanoparticles at the surface. As the precursor, we used H 2 Ti 3 O 7 nanoribbons prepared from sodium titanate nanoribbons by ion exchange. Two cerium sources with an oxidation state of +3 and +4 were used to obtain mixed oxides. HAADF–STEM mapping of the Ce 4+ -modified nanoribbons revealed a thin continuous layer at the surface of the H 2 Ti 3 O 7 nanoribbons, while Ce 3+ cerium ions intercalated partially between the titanate layers. The phase composition and morphology changes were monitored during calcination between 620 °C and 960 °C. Thermal treatment led to the formation of CeO 2 nanoparticles on the surface of the TiO 2 nanoribbons, whose size increased with the calcination temperature. The use of Ce 4+ raised the temperature required for converting H 2 Ti 3 O 7 to TiO 2 -B by approximately 200 °C, and the temperature for the formation of anatase. For the Ce 3+ batch, the presence of cerium inhibited the conversion to rutile. Analysis of cerium oxidation states revealed the existence of both +4 and +3 in all calcined samples, regardless of the initial cerium oxidation state.

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