Impact of Structure and Morphology on Gas Adsorption of Titanate-Based Nanotubes and Nanoribbons

Polona Umek, Pavel Cevc, Adolf Jesih, Alexandre Gloter,§ Christopher P. Ewels, and Denis Aron*
Institute Jozef Stefan, Jamova 39, 1000 Ljubljana, Slovenia, Laboratoire de Physique des Solides, CNRS UMR8502, Universit Paris-Sud, Orsay, France, ICYS, National Institute for Materials Science, Namiki 1-1, Tsukuba 305-0044, Japan, and Faculty of Mathematics and Physics, Jadranska 19, University of Ljubljana, Ljubljana, Slovenia
Chem. Mater., 2005, 17 (24), pp 5945–5950
DOI: 10.1021/cm050928w
Publication Date (Web): November 2, 2005
Copyright © 2005 American Chemical Society

 Institute Jozef Stefan.

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 Université Paris-Sud.

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§

 National Institute for Materials Science.

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*

 Corresponding author. Fax:  + 386 1 4773-191. Tel:  + 386 1 4773-492. E-mail:  denis.arcon@ijs.si.

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 University of Ljubljana.

Abstract

Abstract Image

We report on the synthesis of titania-based nanotubes and nanoribbons prepared by hydrothermal methods, as well as evaluating their structure and adsorption properties. Nanotubes were found to be hollow scrolls with a typical outer diameter of about 10 nm, inner diameter 4−5 nm and length of several hundred nm. The nanoribbons are highly crystalline, typically 40 nm in cross-section and up to a few μm in length. All these samples were exposed to a NO2 atmosphere in order to test their adsorption properties using electron paramagnetic resonance (EPR). The nanotubes were found to have high active surface areas of about 250 m2/g. When exposed to NO2 gas, NO2 molecules tend to physisorb on the nanotube surface via the nonbonding py orbital of the oxygen atoms. In contrast nanoribbons have much smaller active surface areas (30 m2/g). The dominant EPR signal now comes from NO molecules adsorbed on Na+ ions. These results show that titania-based nanotubes and nanoribbons may represent an attractive option for the removal and catalysis of nitrogen oxides in future.

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History

  • Published In Issue November 29, 2005
  • Received May 3, 2005
    Revised Manuscript Received August 30, 2005

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