Photoreactive Anatase Consolidation Characterized by FTIR Spectroscopy

Jeffrey R. S. Brownson, M. Isabel Tejedor-Tejedor, and Marc A. Anderson*
Environmental Chemistry and Technology Program, University of WisconsinMadison, 660 N. Park Street, Madison, Wisconsin 53706
Chem. Mater., 2005, 17 (25), pp 6304–6310
DOI: 10.1021/cm051568f
Publication Date (Web): November 4, 2005
Copyright © 2005 American Chemical Society
*

 To whom correspondence should be addressed. Tel.:  608-262-2674. Fax:  608-262-0454. E-mail:  nanopor@wisc.edu.

Abstract

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Titania (anatase) thin films were consolidated and hardened via UV irradiation when acidic precursor sols were diluted with 1-, 2-, and 3-carbon aliphatic alcohols. Titania sols were adjusted to pH values of 1.4, 2.3, or 3.1 and subsequently diluted with various mole fractions (XROH) of alcohol prior to film deposition. Re-esterification of the titania film surface was confirmed by transmission FTIR (Fourier transform infrared) spectroscopic characterization. In the dark (absence of UV), proton-catalyzed oxidation of the alkoxide functional groups produced a unique monodentate formic acid ligand. This further oxidized to bidentate bicarbonate and carbonate complexes. Given an equivalent fluence of UV light (20 J cm-2, 254 nm), films became harder with increased proton concentration and XROH. UV light promoted formic acid and carbonate/bicarbonate removal by photocatalytic oxidation. The rate of loss of formic acid/bicarbonate species following UV irradiation increased with increasing proton concentration. With respect to carbon chain length, film hardness was found to follow MeOH > EtOH > nPrOH for pH 1.4 and XROH = 0.48.

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History

  • Published In Issue December 13, 2005
  • Received July 18, 2005
    Revised Manuscript Received October 3, 2005

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