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Updated: Sep 21, 2025

Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Indacenodithieno[3,2-b]thiophene-Based Wide Bandgap D-π-A Copolymer for Nonfullerene Organic Solar Cells
Feng Li1,2, Ailing Tang1, Bao Zhang3
1CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190, China.
Abstract:
Herein, a wide-bandgap (2.02 eV) donor-π-acceptor (D-π-A) polymer PIDTT-DTffBTA, composed of a rigid indacenodithieno[3,2-b]thiophene (IDTT) and fluorinated benzo[d][1,2,3]triazole (ffBTA) units as D and A units, respectively, is synthesized. In comparison with its analogue benzodithiophene-alt-benzotriazole copolymer J52 with classic benzodithiophene (BDT) as the D unit, PIDTT-DTffBTA demonstrates a lower-lying HOMO energy level and higher carrier mobilities when paired with a nonfullerene acceptor (NFA) Y6 based on a ladder-type dithienothiophen[3.2-b]-pyrrolobenzothiadiazole central unit. Thus, PIDTT-DTffBTA:Y6 based organic solar cells (OSCs) exhibit an improved power conversion efficiency (PCE) of 11.05% than that of J52:Y6 (7.15%), which is also the highest value for IDTT-based photovoltaic polymers. This result proves that the IDTT unit is also a promising building block to construct not only NFAs but also p-type photovoltaic polymers.
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