Abstract

We report a systematic investigation of the correlations between the electron mobility of polymer acceptors and the photovoltaic performances of all-polymer solar cells (all-PSCs) by using a series of naphthalene diimide (NDI)-based polymer acceptors. Polymer acceptors typically have much lower electron mobility than fullerenes, which is one of the main factors in limiting the performance of all-PSCs. In addition, the anisotropic charge transport properties of the polymers require careful control of their packing structure and orientation suitable for their use in all-PSCs. To control the planarity of the polymer backbone and enhance electron mobility, we introduce three different electron-rich units (i.e., thiophene (T), bithiophene (T2), and thienylene–vinylene–thienylene (TVT)) into the NDI-based polymers. Particularly, P(NDI2OD–TVT) polymers exhibit the highest electron mobility (2.31 cm2 V–1 s–1) in organic field-effect transistors owing to various factors including enhanced degree of coplanarity, st...

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