The influence of the local structure of Fe(III) on the photocatalytic activity of doped TiO(2) photocatalysts

Fe(III)-doped TiO(2) based heterogeneous photocatalysts were prepared by the sol-gel technique (S samples) or flame hydrolysis (F samples). In photocatalytic phenol decomposition, the undoped F-sample performed much better, than the undoped S one. However, for the S samples, photocatalytic activit...

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Elmentve itt :
Bibliográfiai részletek
Szerzők: Bajnóczi Éva Gabriella
Balázs Nándor
Mogyorósi Károly
Srankó Dávid Ferenc
Pap Zsolt
Ambrus Zoltán
Canton Sophie E.
Norén Katarina
Kuzmann Ernő
Vértes Attila
Homonnay Zoltán
Oszkó Albert
Pálinkó István
Sipos Pál Miklós
Dokumentumtípus: Cikk
Megjelent: 2011-03-14
Sorozat:Applied Catalysis B-Environmental 103 No. 1-2
doi:10.1016/j.apcatb.2011.01.033

mtmt:1413093
Online Access:http://publicatio.bibl.u-szeged.hu/97
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245 1 4 |a The influence of the local structure of Fe(III) on the photocatalytic activity of doped TiO(2) photocatalysts  |h [elektronikus dokumentum] /  |c  Bajnóczi Éva Gabriella 
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490 0 |a Applied Catalysis B-Environmental  |v 103 No. 1-2 
520 3 |a Fe(III)-doped TiO(2) based heterogeneous photocatalysts were prepared by the sol-gel technique (S samples) or flame hydrolysis (F samples). In photocatalytic phenol decomposition, the undoped F-sample performed much better, than the undoped S one. However, for the S samples, photocatalytic activity first increased with the increasing Fe(III) concentration, and then passed through a maximum, while Fe(III)-doping in F samples significantly decreased it, even at the smallest dopant level. Since the same dopant caused opposite photocatalytic effects in the two series, their structure was systematically compared to identify the underlying chemical and/or physical reasons. The photocatalysts were first characterized by AAS, DRS, XRD and TEM methods and it has been shown that the differences in the photocatalytic activity cannot be explained by the minor variations in the bulk structural properties of TiO(2). Mossbauer and XP spectroscopic measurements performed on representative samples qualitatively proved that the local structure of Fe(III) is different in the two series. To quantify these effects, Fe-K edge X-ray absorption measurements were performed. From the pre-edge and XANES region it was learnt that Fe(III) was present in a distorted octahedral environment in both series, however, the extent of distortion is much more significant within the S than within the F one. Information obtained from the EXAFS region indicated that the structure of Fe(2)O(3) was much more ordered in the F-series then in the S one and vacancies were more abundant in the S than in the F series. Moreover, the geometry around Fe(III) systematically varied within the S-series, which could explain, why photocatalytic activity passed through a maximum with the increasing Fe(III) concentration in these samples. (C) 2011 Elsevier B.V. All rights reserved. 
700 0 1 |a Balázs Nándor  |e aut 
700 0 1 |a Mogyorósi Károly  |e aut 
700 0 1 |a Srankó Dávid Ferenc  |e aut 
700 0 1 |a Pap Zsolt  |e aut 
700 0 1 |a Ambrus Zoltán  |e aut 
700 0 1 |a Canton Sophie E.  |e aut 
700 0 1 |a Norén Katarina  |e aut 
700 0 1 |a Kuzmann Ernő  |e aut 
700 0 1 |a Vértes Attila  |e aut 
700 0 1 |a Homonnay Zoltán  |e aut 
700 0 1 |a Oszkó Albert  |e aut 
700 0 1 |a Pálinkó István  |e aut 
700 0 1 |a Sipos Pál Miklós  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/97/1/apcatb103%282011%29232.pdf  |z Dokumentum-elérés