Abstract

In the field of all-polymer solar cells, exploring new electron-donating units (D) to match with electron-accepting units (A) is an important subject to promote the performance of D-A-type polymer acceptors. Herein, we developed a fused D unit 2-(thiophen-2-yl)thieno[3,2-b]thiophene (T-TT) derivated from the famous 2-(2-(thiophen-2-yl)vinyl)thiophene (TVT) unit. With classical naphthalene diimide (NDI) as A unit, the new D-A polymer PNDI-T-TT exhibits enhanced absorption coefficient, electron mobility, and miscibility with donor polymer in comparison with the analogous PNDI-TVT polymer. These advantages can be attributed to the enlarged conjugation and reduced rotamers due to the fused T-TT unit, leading to a stronger intermolecular interaction. When blending with the donor polymer PBDB-T, both NDI-based polymers can form better interpenetrating nanostructures than the corresponding blend films with the donor polymer J71. Finally, PBDB-T/PNDI-T-TT device achieves a power conversion efficiency of 6.1%, which is much higher than that of PBDB-T/PNDI-TVT device (4.24%). These results demonstrate that n-type polymer based on fused T-TT unit can ameliorate the absorption coefficient, molecular aggregation, and charge-carrier mobility and consequently achieve an improved photovoltaic performance in comparison with the classic TVT unit.

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