Mobility and decay kinetics of charge carriers in photoexcited PCBMÕPPV blends

The transient photoconductivity of blends of a highly soluble C60 derivative ~PCBM! and a dialkoxyphenylene-vinylene polymer ~MDMO-PPV! has been studied using the electrodeless flash-photolysis timeresolved microwave conductivity technique ~FP-TRMC!. Films approximately 100 nm thick on a quartz substrate were prepared by spin-coating PCBM/PPV solutions with PCBM weight fractions (WPCBM) from 0.2 to 0.95. For all blends, the wavelength dependence of the photoconductivity in the range 420–700 nm closely resembled the photon attenuation spectrum, indicating that photoexcitation of both components contributes to mobile charge carrier formation. The product of the quantum yield for charge separation f and the sum of the charge carrier mobilities Sm was determined from the maximum ~end-of-pulse! value of the transient photoconductivity. On excitation at 500 nm, fSm remained almost constant in going from WPCBM50.2 to 0.6 with an average value of 0.6310 cm/V s. Above WPCBM50.6, fSm increased dramatically, reaching a maximum value of 83310 cm/V s for WPCBM50.85. This effect is attributed to the occurrence of phase separation above WPCBM50.6 and to the resulting formation of highly mobile electrons within PCBM-rich aggregates. The much lower value of fSm observed below WPCBM50.6 is assigned mainly to mobile holes within the polymer component of the blend. Possible explanations for the decrease in fSm with increasing light intensity, found for all blend compositions, are discussed.