Sensitization of Nanocrystalline TiO2 Initiated by Reductive Quenching of Molecular Excited States
Citations Over TimeTop 10% of 1998 papers
Abstract
An alternative mechanism for dye sensitization of wide bandgap semiconductors has been realized: reductive quenching of the dye excited state(s) followed by thermal interfacial electron transfer. The processes were identified using nanosecond-time-resolved absorption and photoluminescence spectroscopies after selective excitation of Ru(deeb)(bpy)2(PF6)2, where bpy is 2,2‘-bipyridine and deeb is 4,4‘-(COOC2H5)2-2,2‘-bipyridine, sensitizers anchored to a nanocrystalline (anatase) TiO2 film immersed in a 0.1 M tetrabutylammonium perchlorate acetonitrile solution with phenothiazine electron donors. With the electrolyte changed to 0.1 M lithium perchlorate, this same assembly undergoes the generally accepted mechanism for dye sensitization: the sensitizer excited state(s) transfer an electron to the semiconductor and is subsequently reduced by the phenothiazine donor.
Related Papers
- → Electrochemical Properties of Hydroxyapatite Crystal Surfaces on Anatase Photocatalysts(2005)13 cited
- → On the synthesis of nanostructured TiO2 anatase phase and the development of the photoelectrochemical solar cell(1999)22 cited
- → Electrode characteristics of nanocrystalline AB5 compounds prepared by mechanical alloying(1998)10 cited
- → A study on the interaction of V2O5/TiO2 (anatase) by high-resolution electron microscopy (hrem)(1986)50 cited
- → GROWTH, SURFACE CHARACTERIZATION, AND REACTIVITY OF TIO2 ANATASE FILMS-EPSCOR(2004)