AI Article Synopsis

  • CeO-TiO is a key mixed oxide known for its catalytic properties, particularly in photocatalysis, and this study explores a method to create 1D TiO nanostructures with CeO nanoparticles attached.
  • The precursor used was HTiO nanoribbons, which were produced from sodium titanate through ion exchange, with different cerium oxidation states (+3 and +4) applied to form the mixed oxide.
  • Calcination processes showed that cerium influences the conversion temperatures of HTiO to TiO-B and inhibits the formation of rutile while both +3 and +4 oxidation states of cerium were detected in all samples after calcination.

Article Abstract

CeO-TiO is an important mixed oxide due to its catalytic properties, particularly in heterogeneous photocatalysis. This study presents a straightforward method to obtain 1D TiO nanostructures decorated with CeO nanoparticles at the surface. As the precursor, we used HTiO 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-modified nanoribbons revealed a thin continuous layer at the surface of the HTiO nanoribbons, while Ce 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 nanoparticles on the surface of the TiO nanoribbons, whose size increased with the calcination temperature. The use of Ce raised the temperature required for converting HTiO to TiO-B by approximately 200 °C, and the temperature for the formation of anatase. For the Ce 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421187PMC
http://dx.doi.org/10.3390/molecules28155838DOI Listing

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