Abstract
A quasi-solid-state photoelectrochemical cell employing a dye-sensitized, nanocrystalline TiO2 electrode and a polymer gel electrolyte has been fabricated. The cells show open-circuit voltages close to 0.6 V and short-circuit currents larger than 3 mA cm-2 under 30 mW cm-2 white light illumination. Fill factors and open circuit voltages of the cell are comparable to those of similar cells with liquid electrolytes. Overall energy conversion efficiencies of 3-5% have been achieved. Photocurrent transients have relatively long rise time constants, indicating that electron transport in the TiO2 electrodes is controlled by a trapping process. At high light intensity the photocurrent rise is followed by a decay process due to the limitation of ion transport in the electrolyte.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 17071-17073 |
| Number of pages | 3 |
| Journal | Journal of Physical Chemistry |
| Volume | 99 |
| Issue number | 47 |
| DOIs | |
| State | Published - 1995 |
ASJC Scopus subject areas
- General Engineering
- Physical and Theoretical Chemistry
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