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Highly Active Photocatalytic TiO2 Powders Obtained by Thermohydrolysis of TiCl4 in Water

Di Paola, Agatino, Bellardita, Marianna, Ceccato, Riccardo, Palmisano, Leonardo, Parrino, Francesco·2009·The Journal of Physical Chemistry C

Abstract

Highly active photocatalytic TiO 2 samples were synthesized by thermohydrolysis of TiCl 4 in water at 100 °C. Rutile, binary mixtures of anatase and rutile or anatase and brookite or ternary mixtures of anatase, brookite, and rutile were obtained depending on the TiCl 4 /H 2 O ratio. Rietveld refinements were employed to evaluate the crystalline phases and composition of the mixtures. The effect of the aging time on the phase composition was also studied. The band gap values of the samples were obtained by the diffuse reflectance spectra. The position of the flat band potentials of anatase, brookite, and rutile was determined measuring the photovoltage as a function of the suspension pH. From these data, the relative positions of the energy bands of the three semiconductors were estimated. 4-Nitrophenol photodegradation was used to evaluate the photoactivity of the various samples. Some powders were more active than Degussa P25. The most efficient samples consisted of a ternary mixture of anatase, brookite, and rutile. The high photocatalytic activity was explained by the presence of junctions among different polymorphic TiO 2 phases that enhance the separation of the photogenerated electron−hole pairs, hindering their recombination.

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Metadata

Authors
Di Paola, A., Bellardita, M., Ceccato, R., Palmisano, L., & Parrino, F.
Venue
The Journal of Physical Chemistry C
Published
2009-07-30
Volume
113
Issue
34
Pages
15166-15174
ISSN
  • 1932-7447 (ISSN-L)
  • 1932-7455
OpenAlex
W2055052122
Cited by
169
References
2
FWCI
5.14
Type
journal article
Language
en
Open access
closed

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Di Paola, A., Bellardita, M., Ceccato, R., Palmisano, L., & Parrino, F. (2009). Highly Active Photocatalytic TiO2 Powders Obtained by Thermohydrolysis of TiCl4 in Water. The Journal of Physical Chemistry C. https://doi.org/10.1021/jp904673e

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