Electron transfer from TiO to iodine/iodide electrolytes proceeds via reduction of either I or uncomplexed I (free iodine), but which route predominates has not previously been determined. By measurement of the electron lifetime while independently varying free iodine or I concentrations, we find the lifetime is correlated with free-iodine concentration and independent of I concentration. This trend supports the hypothesis that electron recombination to the electrolyte occurs predominantly by iodine reduction rather than reduction of triiodide.Peer reviewe

We observe anisotropy in the polarization flux generated in a GaAs/AlAs photonic cavity by optical illumination, equivalent to spin currents in strongly coupled microcavities. Polarization rotation of the scattered photons around the Rayleigh ring is due to the TE-TM splitting of the cavity mode. Resolving the circular polarization components of the transmission reveals a separation of the polarization flux in momentum space. These observations constitute the optical analogue of the spin Hall effect.

Polymer morphology affects quantum efficiency. The influence of polymer morphology on the emission from charge transfer states within donor-acceptor (D-A) polydioctylfluorene derivatives is investigated. Two D-A copolymers, comprising one- and two-electron-donating triphenylamines substituted into the electron-accepting dioctylfluorene repeat unit were studied. Time-resolved emission spectra (with a resolution of 330 fs) in both liquid and glass phase isolate nuclear relaxation to the large-amplitude motion of the triphenylamine moiety about the single bond, analogous to the twisted intramolecular charge-transfer (TICT) model. The charge separation in the polymers' emitting states is therefore increased, suggesting a potential approach to enhance quantum efficiency in devices otherwise limited by exciton recombination.