Ultrafast Electron Injection: Implications for a Photoelectrochemical Cell Utilizing an Anthocyanin Dye-Sensitized TiO2Nanocrystalline Electrode

作者：Nerine J. Cherepy, Greg P. Smestad, Michaël Grätzel, Jin Zhong Zhang · 发表于：The Journal of Physical Chemistry B · 年份：1997 · DOI：10.1021/jp972197w · 被引用次数：605 · 研究领域：TiO2 Photocatalysis and Solar Cells、Advanced Photocatalysis Techniques、Advanced oxidation water treatment

A photoelectrochemical cell utilizing flavonoid anthocyanin dyes extracted from blackberries, along with colloidal TiO 2 powder, is shown to convert sunlight to electrical power at an efficiency of 0.56% under full sun. Fluorescence quenching is observed for the excited state of the TiO 2 -adsorbed anthocyanin dye, cyanin, and the photocurrent spectrum correlates well with the optical absorption of the cyanin-sensitized TiO 2 nanocrystalline film. The incident photon-to-current efficiency of 19% at the peak of the visible absorption band of the dye, the open-circuit voltages of 0.5−0.4 V, and short-circuit photocurrents of 1.5−2.2 mA/cm 2 are remarkable for such a simple system and suggest efficient charge carrier injection. The ultrafast excited-state dynamics of cyanin in solution are compared with those of surface-adsorbed cyanin on TiO 2 and ZrO 2 colloids, as well as complexed with Al(III) ions. A transient absorption signal with a risetime of <100 fs for cyanin-sensitized TiO 2 nanoparticles is assigned to electrons injected from the dye to TiO 2 . This signal is fit to a double-exponential decay with time constants of 0.52 and 67 ps. The 0.52 ps component is due to trapping of conduction band electrons or to fast direct recombination with the dye cation, while the 67 ps decay is attributed to trap state mediated indirect recombination. In contrast, stimulated emission with a 2.6 ps decay time is observed for cyanin in solution, cyanin on ZrO 2, and cyanin complexed wit...