Electron Transfer Dynamics in Nanocrystalline Titanium Dioxide Solar Cells Sensitized with Ruthenium or Osmium Polypyridyl Complexes
Abstract
The electron transfer dynamics in solar cells that utilize sensitized nanocrystalline titanium dioxide photoelectrodes and the iodide/triiodide redox couple have been studied on a nanosecond time scale. The ruthenium and osmium bipyridyl complexes Ru(H_2L')_2(CN)_2, Os(H_2L')_2(CN)_2, Ru(H_2L')_2(NCS)_2, and Os(H_2L')_2(NCS)_2, where H_2L' is 4,4'-dicarboxylic acid 2,2'-bipyridine, inject electrons into the semiconductor with a rate constant >10^8 s^(-1). The effects of excitation intensity, temperature, and applied potential on the recombination reaction were analyzed using a second-order kinetics model. The rates of charge recombination decrease with increasing driving force to the oxidized sensitizer, indicating that charge recombination occurs in the Marcus inverted region. The electronic coupling factors between the oxidized sensitizer and the injected electrons in TiO_2 and the reorganization energies for the recombination reaction vary significantly for the different metal complexes. The charge recombination rates are well described by semiclassical electron transfer theory with reorganization energies of 0.55−1.18 eV. Solar cells sensitized with Ru(H_2L')_2(CN)_2, Os(H_2L')_2(CN)_2, and Ru(H_2L')_2(NCS)_2 have favorable photoelectrochemical characteristics, and iodide is oxidized efficiently. In contrast, iodide oxidation limits the efficiency of cells based on sensitization of TiO_2 with Os(H_2L')_2(NCS)_2. The observation that charge recombination occurs in the Marcus inverted region has important implications for the design of molecular sensitizers in nanocrystalline solar cells operated under our experimental conditions.
Additional Information
© 2001 American Chemical Society. Received: July 18, 2000; In Final Form: September 20, 2000. Publication Date (Web): December 19, 2000. We acknowledge Dr. George Coia of Caltech for useful discussions. This work was supported by the Department of Energy, Office of Basic Energy Sciences (D.K., M.S.F., N.S.L.), and by the NSF (H.B.G., J.R.W.). We also acknowledge a generous gift in support of work on TiO2 photoelectrochemistry to Caltech by the DuPont Company.Attached Files
Supplemental Material - jp002545l_s.pdf
Files
Name | Size | Download all |
---|---|---|
md5:2b204b2a59cbb68001cbbd47180c5023
|
28.3 kB | Preview Download |
Additional details
- Eprint ID
- 75156
- Resolver ID
- CaltechAUTHORS:20170315-151836987
- Department of Energy (DOE)
- NSF
- DuPont Company
- Created
-
2017-03-16Created from EPrint's datestamp field
- Updated
-
2021-11-15Created from EPrint's last_modified field