an electron donating conjugated polymer and an electron accepting small molecule, pure phases of donor and/or acceptor often coexist alongside a molecularly intermixed donor:acceptor phase. [5-9] The overall blend morphology, and the proportions and lengthscales of such pure and intermixed domains have been shown to be critical in determining device performance. [5-9] In recent years, the development of a range of nonfullerene acceptors (NFAs) has enabled, when blended with complementary absorbing donor polymers, impressive advances in OSC performance. [10,11] In the study herein, we focus on the recently reported PTQ10:IDIC blend system, which has been suggested to be particularly promising for low cost commercial application. [2] We find this blend system to be remarkably crystalline, and investigate the impact of this high crystallinity upon the exciton and charge carrier dynamics determining device performance. In BHJ blends, a large donor/acceptor interfacial area facilitates the exciton dissociation required for efficient photocurrent generation. [12,13] However, this donor/acceptor interface can also yield interfacial electron-hole pairs, often referred to as charge transfer (CT) states. [12,14-17] CT states formed in the highly intermixed regions of such blends have been reported to give rise Herein the morphology and exciton/charge carrier dynamics in bulk heterojunctions (BHJs) of the donor polymer PTQ10 and molecular acceptor IDIC are investigated. PTQ10:IDIC BHJs are shown to be particularly promising for low cost organic solar cells (OSCs). It is found that both PTQ10 and IDIC show remarkably high crystallinity in optimized BHJs, with GIWAXS data indicating pi-pi stacking coherence lengths of up to 8 nm. Exciton-exciton annihilation studies indicate long exciton diffusion lengths for both neat materials (19 nm for PTQ10 and 9.5 nm for IDIC), enabling efficient exciton separation with half lives of 1 and 3 ps, despite the high degree of phase segregation in this blend. Transient absorption data indicate exciton separation leads to the formation of two spectrally distinct species, assigned to interfacial charge transfer (CT) states and separated charges. CT state decay is correlated with the appearance of additional separate charges, indicating relatively efficient CT state dissociation, attributed to the high crystallinity of this blend. The results emphasize the potential for high material crystallinity to enhance charge separation and collection in OSCs, but also that long exciton diffusion lengths are likely to be essential for efficient exciton separation in such high crystallinity devices.