Abstract
We present a photophysical and device-based investigation of a new bipyridyl-NCS ruthenium complex sensitizer with an extended n system, in both sensitized TiO2 and incorporated into solid-state dye-sensitized solar cells. We compare this new sensitizer to an analog dye without the extended π system. We observe very similar excited-state absorption spectra and charge recombination kinetics for the two systems. However, the π-extended senstizer has a phenomenally enhanced molar extinction coefficient which translates into far greater light harvesting and current collection in solid-state dye-sensitized solar cells. We also infer from transient photovoltage measurements that positioning the pendent extended n system away from the TiO2 surface has induced a favorable dipole shift, generating enhanced open-circuit voltage. The resulting power conversion efficiency for the solar cell has been increased from 2.4% to 3.2% when comparing the new sensitizer to an analogy with no pendent group. © 2008 American Chemical Society.
Cite
CITATION STYLE
Snaith, H. J., Karthikeyan, C. S., Petrozza, A., Teuscher, J., Moser, J. E., Nazeeruddin, M. K., … Grätzel, M. (2008). High extinction coefficient “antenna” dye in solid-state dye-sensitized solar cells: A photophysical and electronic study. Journal of Physical Chemistry C, 112(20), 7562–7566. https://doi.org/10.1021/jp801714u
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.