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Polymer solar cells possess a promising perspective for generating renewable energy at affordable costs, provided their performance and durability can be improved considerably. To this end, several experimental and theoretical techniques have been devised recently, establishing a direct link between local morphology, local opto-electronic properties and device performance. However, their reliability is still unclear to this day. Here, we demonstrate by using a recently developed particle-based multiscale solar cell approach and comparing its results with the ones of a field-based solar cell algorithm that inter-mixing of the electron-donor(D)- and -acceptor(A)-type of segments in a lamellar-like poly(9,9’-dioctylfluorene-co-bis-N,N'-(4-butylphenyl)-bis-N,N'-phenyl-1,4-phenylene-diamine)-poly(9,9'-dioctylfluorene-co-benzothiadiazole) (PFB-F8BT) blend causes that the major part of the charge generation and charge transport takes place inside the nanophases of the nanostructured polymer solar cells in agreement with recent experimental measurements and not, as commonly believed, at the visible domain boundaries of the DA interface. Moreover, we show that the contribution of the exciton dissociation efficiency to the internal quantum efficiency, due to inter-monomeric mixing, is significant and cannot be neglected in simulation studies at the nanoscale. Finally, we demonstrate that keto-defects on the fluorene moiety of the F8BT phase, induced by photo-oxidation, causes a simultaneous increase of the intra-chain contribution and decrease of the inter-chain contribution to the electronic current density, whereas in the reduced form the difference between both contributions is significantly smaller. This antagonistic effect leads to keto-induced electron trapping, resulting in a deteriorated electronic transport efficiency in devices with a photo-oxidized F8BT phase. |
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