Illumination Intensity Dependence of the Photovoltage in Nanostructured TiO2 Dye-Sensitized Solar Cells
- 27 July 2005
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry B
- Vol. 109 (33) , 15915-15926
- https://doi.org/10.1021/jp051515l
Abstract
The open-circuit voltage (Voc) dependence on the illumination intensity (Φ0) under steady-state conditions in both bare and coated (blocked) nanostructured TiO2 dye-sensitized solar cells (DSSCs) is analyzed. This analysis is based on a recently reported model [Bisquert, J.; Zaban, A.; Salvador, P. J. Phys. Chem. B2002, 106, 8774] which describes the rate of interfacial electron transfer from the conduction band of TiO2 to acceptor electrolyte levels (recombination). The model involves two possible mechanisms: (1) direct, isoenergetic electron injection from the conduction band and (2) a two-step process involving inelastic electron trapping by band-gap surface states and subsequent isoenergetic transfer of trapped electrons to electrolyte levels. By considering the variation of Voc over a wide range of illumination intensities (1010 < Φ0 < 1016 cm-2 s-1), three major regions with different values of dVoc/dΦ0 can be distinguished and interpreted. At the lower illumination intensities, recombination mainly involves localized band-gap, deep traps at about 0.6 eV below the conduction band edge; at intermediate photon fluxes, recombination is apparently controlled by a tail of shallow traps, while, for high enough Φ0 values, conduction band states control the recombination process. The high Φ0 region is characterized by a slope of dVoc/d log Φ0 ≅ 60 mV, which indicates a recombination of first order in the free electron concentration. The study, which was extended to different solar cells, shows that the energy of the deep traps seems to be an intrinsic property of the nanostructured TiO2 material, while their concentration and also the density (ϑt ≈ 1018−1019 cm-3) and distribution of shallow traps, which strongly affects the shape of the Voc vs Φ0 curves, change from sample to sample and are quite sensitive to the electrode preparation. The influence of the back-reaction of electrons from the fluorine-doped tin oxide (FTO) conducting glass substrate with electrolyte tri-iodide ions on the Voc vs Φ0 dependence characteristic of the DSSC is analyzed. It is concluded that this back-reaction route can be neglected, even at low light intensities, when its rate (exchange current density, j0), which can vary over 4 orders of magnitude depending on the type of FTO used, is low enough (j0 ≤10-8A cm-2). The comparison of Voc vs Φ0 measurements corresponding to different DSSCs with and without blocking of the FTO−electrolyte contact supports this conclusion.Keywords
This publication has 24 references indexed in Scilit:
- Determination of Rate Constants for Charge Transfer and the Distribution of Semiconductor and Electrolyte Electronic Energy Levels in Dye-Sensitized Solar Cells by Open-Circuit Photovoltage Decay MethodJournal of the American Chemical Society, 2004
- Cyclic Voltammetry Studies of Nanoporous Semiconductors. Capacitive and Reactive Properties of Nanocrystalline TiO2 Electrodes in Aqueous ElectrolyteThe Journal of Physical Chemistry B, 2002
- Computer Simulations of Charge Transport in Dye-Sensitized Nanocrystalline Photovoltaic CellsThe Journal of Physical Chemistry B, 2001
- Electrochemical Investigation of Traps in a Nanostructured TiO2 FilmThe Journal of Physical Chemistry B, 2001
- Effect of the Surface-State Distribution on Electron Transport in Dye-Sensitized TiO2 Solar Cells: Nonlinear Electron-Transport KineticsThe Journal of Physical Chemistry B, 2000
- Carrier transport in nanoporousfilmsPhysical Review B, 2000
- Intensity Dependence of the Back Reaction and Transport of Electrons in Dye-Sensitized Nanocrystalline TiO2Solar CellsThe Journal of Physical Chemistry B, 2000
- Electron Trapping in Porphyrin-Sensitized Porous Nanocrystalline TiO2 ElectrodesThe Journal of Physical Chemistry, 1996
- Artificial Photosynthesis. 2. Investigations on the Mechanism of Photosensitization of Nanocrystalline TiO2 Solar Cells by Chlorophyll DerivativesThe Journal of Physical Chemistry, 1994
- Effect of surface chelation on the energy of an intraband surface state of a nanocrystalline titania filmThe Journal of Physical Chemistry, 1993