A simple analytical function, based on the multiple trapping model, is used to describe the bimolecular recombination of charge carriers in a bulk heterojunction (BHJ) film in the presence of an exponential energetic tail of localized hole "trap" states. The function is used to fit charge carrier decay data from an unannealed P3HT/PCBM film measured by transient absorption. The analysis assumes that only free holes participate in recombination and transport. This implies an effective recombination rate coefficient which varies with the ratio of free to trapped holes. The fit parameters yield a bimolecular recombination constant for free holes with free electrons (k 0 = 3.4 Â 10 -12 cm 3 s -1 ) and information about the distribution of trap states (trap distribution parameter β = 0.29). Assuming the Langevin recombination limit, the analysis yields a concentrationdependent effective hole mobility saturating at μ 0 ≈ 7 Â 10 -2 cm 2 V -1 s -1 . This approach should be useful to compare BHJs in a consistent and meaningful manner.SECTION Electron Transport, Optical and Electronic Devices, Hard Matter E fficient photoinduced charge separation has been widely observed in organic film blends employing materials with different chemical potentials. There are extensive efforts to use such charge photogeneration for the photovoltaic conversion of solar energy. 1 The formation of a bulk heterojunction (BHJ), which is an interpenetrating network of different organic materials where the domain size of each phase is on the nanometre scale, facilitates efficient photoinduced charge separation. This is because the dissociation of photogenerated excitons into charge-carrying polarons (electrons and holes) generally occurs at the interface between the materials, and exciton diffusion lengths are typically only a few nanometers. 2 However, the enhanced charge dissociation achieved within a BHJ relative to that in a standard heterojunction comes at the cost of increased bimolecular recombination (recombination of electron and hole polaron charge carriers) due to the high interfacial area between the phases and the longer charge collection pathways in a photovoltaic device.Recently, it was shown that bimolecular recombination can severely limit the performance (particularly the opencircuit photovoltage, V oc ) of BHJ organic solar cells. 3 The work also indicated that the mobility of charge carriers was dependent on the concentration of separated charge in the device. 4 This is thought to be related to trapping of charge carriers in localized electronic states within the band gap of bulk organic materials. 5 Numerical simulations based on trapping/detrapping events using an exponential distribution of trap states have proven very successful in describing bimolecular recombination in BHJs, where recombination events are limited by the transport of charge carriers through a trap-rich medium. 6 To understand and optimize the function of devices based on organic materials, it is important to have a set of characterization tools enabling fu...