Maintaining particle size in the transformation of anatase to rutile titania nanostructures

  • Andrew Ogden
  • , James A. Corno
  • , Jung Il Hong
  • , Andrei Fedorov
  • , James L. Gole

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

We study the temperature-dependent transformation of two distinctly synthesized TiO2 nanoparticles from the anatase to the rutile phase. These studies are carried out over the temperature range extending from room temperature to an excess of 800°C where the anatase to rutile conversion is found to occur. Results obtained for both a sol-gel-generated nanocolloid (3-20 nm) and a sol-gel-generated micelle nanostructure (∼40nm) are evaluated. While the TiO2 nanocolloid structures aggregate to form larger crystallites as a function of increasing temperature with sizes comparable to the sol-gel-generated micelle structures, the resulting anatase aystattites, which are of a diameter 40-50 nm, appear to transform to comparable or slightly smaller rutile structures at 800°C. This is in contrast to the transformation to larger rutile structures, observed for larger anatase particles. The importance of kinetic effects is considered as it enhances the rate of anatase to rutile conversion. These characteristics are established using a combination of Raman spectroscopic, X-ray diffraction, and scanning electron microscopy. The relative playoffs of the Raman and X-ray diffraction techniques are considered as they are used for the analysis of particles at the nanoscale, especially when phase transformations are evaluated.

Original languageEnglish
Pages (from-to)2898-2906
Number of pages9
JournalJournal of Physics and Chemistry of Solids
Volume69
Issue number11
DOIs
StatePublished - Nov 2008

Bibliographical note

Funding Information:
We acknowledge Dan “The Man” Jackson, whose incredible enthusiasm, as an NSF-REU student, for the development of novel catalytic films first led us on this path. In addition, the generous aid of Dr. Samuel Graham in providing access to his lab and Raman spectrometer is greatly appreciated. We also are grateful to the referees of this manuscript for their very helpful comments. Partial support for this work was provided by a NIRT grant from the National Science Foundation (CTS-0608896).

Keywords

  • Electron diffraction
  • Electron microscopy
  • Nanostructures
  • Raman spectroscopy
  • Semiconductors

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