Ultrafast Transient Spectroscopy of Polymer/Fullerene Blends for Organic Photovoltaic Applications

作者：Singh Sanjeev; Vardeny Zeev Valy^*

来源：Materials, 2013, 6(3): 897-910.

DOI：10.3390/ma6030897

• transient spectroscopy
• organic photovoltaic
• donor-acceptor blends
• charge-transfer excitons

We measured the picoseconds (ps) transient dynamics of photoexcitations in blends of regio-regular poly(3-hexyl-thiophene) (RR-P3HT) (donors-D) and fullerene (PCBM) (acceptor-A) in an unprecedented broad spectral range of 0.25 to 2.5 eV. In D-A blends with maximum domain separation, such as RR-P3HT/PCBM, with (1.2:1) weight ratio having solar cell power conversion efficiency of similar to 4%, we found that although the intrachain excitons in the polymer domains decay within similar to 10 ps, no charge polarons are generated at their expense up to similar to 1 ns. Instead, there is a build-up of charge-transfer (CT) excitons at the D-A interfaces having the same kinetics as the exciton decay. The CT excitons dissociate into separate polarons in the D and A domains at a later time (>1 ns). This "two-step" charge photogeneration process may be typical in organic bulk heterojunction cells. We also report the effect of adding spin 1/2 radicals, Galvinoxyl on the ultrafast photoexcitation dynamics in annealed films of RR-P3HT/PCBM blend. The addition of Galvinoxyl radicals to the blend reduces the geminate recombination rate of photogenerated CT excitons. In addition, the photoexcitation dynamics in a new D-A blend of RR-P3HT/Indene C60 trisadduct (ICTA) has been studied and compared with the dynamics in RR-P3HT/PCBM.

• 出版日期2013-3