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Transient Photocurrent Response of Dye-Sensitized Porous Nanocrys1Alline TiO2 Electrodes

Published online by Cambridge University Press:  15 February 2011

Albert Goossens
Affiliation:
Delft University of Technology, Laboratory for Applied Inorganic Chemistry, Julianalaan 136, 2628 BL Delft, The Netherlands, a.goossens@stm.tudelft.nl
G. K. Boschloo
Affiliation:
Delft University of Technology, Laboratory for Applied Inorganic Chemistry, Julianalaan 136, 2628 BL Delft, The Netherlands, a.goossens@stm.tudelft.nl
J. Schoonman
Affiliation:
Delft University of Technology, Laboratory for Applied Inorganic Chemistry, Julianalaan 136, 2628 BL Delft, The Netherlands, a.goossens@stm.tudelft.nl
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Abstract

In order to investigate the fundamentals of electron migration in nanostructured metal-oxide semiconductors, the transient photocurrent response of dye-sensitized porous nanocrystalline TiO2 is studied. The time-resolved photocurrent response at light steps or pulses shows a faster transient upon increasing the light intensity. Intensity-modulated photocurrent spectroscopy (IMPS) reveals that the transient photocurrent is dominated by two time constants, i.e. the geometrical one and a characteristic time related to electron trapping. A theoretical model is derived in which the occupation dynamics of a single electron trap is considered using Shockley-Read-Hall kinetics. The geometrical RC time of the electrode is also included. Excellent agreement between this model and the measured IMPS spectra is obtained.

Type
Research Article
Copyright
Copyright © Materials Research Society 1997

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References

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