Synthesis, characterization and activity of photocatalytic SOL-GEL TiO2 powders and electrodes
The efficiency of photoelectrocatalytic processes is strongly influenced by the electrode type and synthesis procedure. This work reports the sol-gel synthesis and characterization of TiO2 and Fe-doped TiO2 powders and electrodes as a function of pH and preparation temperatures and the correlation o...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2009 |
| País: | España |
| Institución: | Universidad Rey Juan Carlos |
| Repositorio: | BURJC-Digital. Repositorio Institucional de la Universidad Rey Juan Carlos |
| OAI Identifier: | oai:burjcdigital.urjc.es:10115/3987 |
| Acceso en línea: | http://hdl.handle.net/10115/3987 |
| Access Level: | acceso abierto |
| Palabra clave: | Medio Ambiente 23 Química |
| Sumario: | The efficiency of photoelectrocatalytic processes is strongly influenced by the electrode type and synthesis procedure. This work reports the sol-gel synthesis and characterization of TiO2 and Fe-doped TiO2 powders and electrodes as a function of pH and preparation temperatures and the correlation of their photoelectrochemical properties with their activity for azo dye decolourization. pH is shown to be the variable that most influences the formation of the TiO2 crystalline phases, the photocurrents of the electrodes, and consequently their photocatalytic activity. Electrodes synthesized at low pH and heated at temperatures below ~ 600 oC show a significant increase in the photocurrent recorded in the presence of methanol. This is attributed to suppression of the charge recombination rather than to a conventional current-doubling mechanism. The photocatalytic activities of the electrodes show a good correlation with the photocurrent measured in the presence of methanol. The mechanistic implications of this correlation are discussed. Iron-doping reduces the activity of the sol-gel electrodes for dye decolourisation. This contrasts with previous results for bacteria disinfection, which is believed to proceed by a hydroxyl radical mechanism. Consequently, it may be that the behaviour of iron as recombination centres or as trapping sites that improve the separation charges may depend on whether the photoelectrocatalytic reaction proceeds by a hydroxyl radical mechanism, as was shown for deactivation of E. coli or by direct hole-transfer, as is suggested by the parallels between dye decolouration and the electrode response to methanol that are reported in this paper. |
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