The dissociation efficiency of bound electron-hole pairs at the donor-acceptor interface in bulk heterojunction solar cells is partly limited due to the low dielectric constant of the polymer:fullerene blend. We investigate the photocurrent generation in blends consisting of a fullerene derivative and an oligo(oxyethylene) substituted poly(p-phenylene vinylene) (PPV) derivative with an enhanced relative permittivity of 4. It is demonstrated that in spite of the relatively low hole mobility of the glycol substituted PPV the increase in the spatially averaged permittivity leads to an enhanced charge dissociation of 72% for these polymer:fullerene blends.
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Lenes et al. (2008) studied this question.
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