Darin W. Laird

Study of photoexcitations in poly(3-hexylthiophene) for photovoltaic applications

We used a variety of steady state and transient optical techniques for studying the primary and steady state photoexcitations in pristine films of poly(3-hexylthiophene) [P3HT] with different molecular weight used for organic photovoltaic solar cells. The employed techniques include picosecond transient and steady state photoluminescence and photomodulation spectroscopies, laser action, and doping induced absorption. We show that solar cell device qualities based on donor-acceptor blends of the P3HT polymers with substituted fullerene molecules crucially depend on the polymer properties, which can be readily discerned by the steady state photomodulation technique. This technique can, therefore, be applied to specific polymer donors for estimating their solar cell device properties prior to actually fabricating an optimal device.

Ultrafast transient spectroscopy of nano-domains of polymer/fullerene blend for organic photovoltaic applications

We measured the picoseconds (ps) transient photomodulation (PM) dynamics of photoexcitations in blends of regio-regular poly(3-hexyl-thiophene) [RR-P3HT] (donors-D) and indene-C60 bisadduct (fullerene derivative) [ICBA] (acceptor-A) that phase-separate into D- and A-nano-domains, in a broad spectral range from 0.25 to 2.5 eV; in comparison with steady state PM spectra. We correlate our measurements with organic photovoltaic solar cell performance made from the same D and A materials. In D-A blends of RR-P3HT/ICBA with (1.2:1) weight ratio having solar cell power conversion efficiency of ∼5.1%, we found that although the intrachain excitons in the polymer nano-domains decay within ∼10 ps, no charge polarons are generated on their expense up to ∼1 ns. Instead, there is a built-up of charge-transfer (CT) excitons at the D-A domain interfaces that occurs with the same kinetics as the exciton decay. The CT excitons dissociate into separate polarons in the D- and A-nano-domains at a much later time (≫1 ns). Thi...