Electron transfer from photoexcited TiO2 to Chelating alizarin molecules: Reversible photochromic effect in Alizarin@TiO2 under UV irradiation

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  • Universidad Nacional de Mar del Plata
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OriginalspracheEnglisch
Seiten (von - bis)1077-1083
Seitenumfang7
FachzeitschriftChemPhysChem
Jahrgang10
Ausgabenummer7
Frühes Online-Datum4 Mai 2009
PublikationsstatusVeröffentlicht - 11 Mai 2009

Abstract

Reduction of alizarin molecules coupled to TiO2 nanoparticles (A@TiO2) occurs on UV irradiation in the presence of a sacrificial electron donor. Evidence is presented that reduction is mediated by conduction-band electrons and yields a 1,2,9,10-tetrahydroxyanthracene species which remains coupled to the TiO2 nanoparticles. The spectrum of the reduced complex displays two overlapping broad bands centred at 480 and 650 nm which can harvest visible photons besides 900 nm, in agreement with theoretical predictions by TDDFT. The potential relevance of the dual-redox behaviour of strongly TiO2 coupled anthraquinone dyes in the field of photocatalysis and in connection with their utilization in the development of dye-sensitized TiO2 solar cells is briefly discussed.

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Electron transfer from photoexcited TiO2 to Chelating alizarin molecules: Reversible photochromic effect in Alizarin@TiO2 under UV irradiation. / Iorio, Yesica Di; Brusa, Marta A.; Feldhoff, Armin et al.
in: ChemPhysChem, Jahrgang 10, Nr. 7, 11.05.2009, S. 1077-1083.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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abstract = "Reduction of alizarin molecules coupled to TiO2 nanoparticles (A@TiO2) occurs on UV irradiation in the presence of a sacrificial electron donor. Evidence is presented that reduction is mediated by conduction-band electrons and yields a 1,2,9,10-tetrahydroxyanthracene species which remains coupled to the TiO2 nanoparticles. The spectrum of the reduced complex displays two overlapping broad bands centred at 480 and 650 nm which can harvest visible photons besides 900 nm, in agreement with theoretical predictions by TDDFT. The potential relevance of the dual-redox behaviour of strongly TiO2 coupled anthraquinone dyes in the field of photocatalysis and in connection with their utilization in the development of dye-sensitized TiO2 solar cells is briefly discussed.",
keywords = "Charge transfer, Electron transfer photochromism, Quinones, Semiconductors",
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T1 - Electron transfer from photoexcited TiO2 to Chelating alizarin molecules

T2 - Reversible photochromic effect in Alizarin@TiO2 under UV irradiation

AU - Iorio, Yesica Di

AU - Brusa, Marta A.

AU - Feldhoff, Armin

AU - Grela, María A.

PY - 2009/5/11

Y1 - 2009/5/11

N2 - Reduction of alizarin molecules coupled to TiO2 nanoparticles (A@TiO2) occurs on UV irradiation in the presence of a sacrificial electron donor. Evidence is presented that reduction is mediated by conduction-band electrons and yields a 1,2,9,10-tetrahydroxyanthracene species which remains coupled to the TiO2 nanoparticles. The spectrum of the reduced complex displays two overlapping broad bands centred at 480 and 650 nm which can harvest visible photons besides 900 nm, in agreement with theoretical predictions by TDDFT. The potential relevance of the dual-redox behaviour of strongly TiO2 coupled anthraquinone dyes in the field of photocatalysis and in connection with their utilization in the development of dye-sensitized TiO2 solar cells is briefly discussed.

AB - Reduction of alizarin molecules coupled to TiO2 nanoparticles (A@TiO2) occurs on UV irradiation in the presence of a sacrificial electron donor. Evidence is presented that reduction is mediated by conduction-band electrons and yields a 1,2,9,10-tetrahydroxyanthracene species which remains coupled to the TiO2 nanoparticles. The spectrum of the reduced complex displays two overlapping broad bands centred at 480 and 650 nm which can harvest visible photons besides 900 nm, in agreement with theoretical predictions by TDDFT. The potential relevance of the dual-redox behaviour of strongly TiO2 coupled anthraquinone dyes in the field of photocatalysis and in connection with their utilization in the development of dye-sensitized TiO2 solar cells is briefly discussed.

KW - Charge transfer

KW - Electron transfer photochromism

KW - Quinones

KW - Semiconductors

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DO - 10.1002/cphc.200800752

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VL - 10

SP - 1077

EP - 1083

JO - ChemPhysChem

JF - ChemPhysChem

SN - 1439-4235

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