No abstract

In this paper, we compare the charge recombination dynamics observed in films comprising poly-(3-hexylthiophene) blended with three fullerene derivatives: PCBM and two alternative pyrazolinofullerenes. Transient absorption data indicate that replacement of PCBM with either of the pyrazolinofullerene derivatives results in a transition from bimolecular to monomolecular (geminate) recombination dynamics. We show that this transition cannot be explained by a difference in interfacial energetics. However, this transition does correlate with nanomorphology data which indicate that both pyrazolinofullerenes yield a much finer phase segregation, with correspondingly smaller domain sizes, than observed with PCBM. Our results therefore provide clear evidence of the role of nanomorphology in determining the nature of recombination dynamics in such donor/acceptor blends.

The regioselectivity of the cycloaddition of N-methylazomethine ylide to C70 can be modified by using microwave irradiation as the source of energy. Under microwave irradiation and by choosing the appropriate solvent and irradiation power, the 5-6 isomer is the major product, a situation that is in contrast to conventional heating where the 1-2 isomer predominates. Moreover, isomer 7-21, which represents 13% of monoadducts under classical heating, is not formed under microwave irradiation and with ODCB as solvent. Theoretical calculations predict an asynchronous mechanism and suggest that the modification of the regiochemical outcome is related to the relative energies and hardnesses of the transition structures involved.

A new family of fullerene-based compounds, namely, soluble [60]- and [70]fullerene homodimers and the [60]/[70]heterodimer linked through 2-pyrazolino-pyrrolidino bridges, has been synthesised by simple procedures and in high yield. Electrochemical studies confirm their suitability to act as electron acceptors in combination with poly(3-hexylthiophene-2,5-diyl) (P3HT). Their optical properties in solution and in the solid state were studied. A significantly stronger absorption in [70]fullerene-containing dimers relative to [60]homodimer in solution in the visible range was observed. Furthermore, in all donor-acceptor blends studied an efficient charge transfer was observed by means of photoluminescence (PL), photoinduced absorption and light-induced electron spin resonance spectroscopy. The [70]homodimer was found to be a distinctive species, being the strongest PL quencher and most efficient acceptor with the longest lifetime of the charge-separated (polaron) states. As a consequence, bulk-heterojunction solar cells based on this novel [70]homodimer blended with P3HT demonstrated the highest quantum and power conversion efficiencies of 37 and 1 %, respectively, compared to those of [60]fullerene dimers.