The backbone shape of semiconducting
polymers strongly affects
their electronic properties and morphologies in films, yet the conventional
design principle for building blocks focuses on using linear main
chains to maintain high crystallinity. Here, we developed a V-shaped
unit, triphenyleno[1,2-c:7,8-c′]bis([1,2,5]thiadiazole)
(TPTz), featuring two 1,2,5-thiadiazole rings fused to a triphenylene
core with strong electron-withdrawing properties and an extended conjugation
plane. We used TPTz to prepare a highly soluble copolymer, PTPTz–indacenodithiophene
(IDT), which exhibited a wide bandgap of 1.94 eV and energy levels
suitable for the donor polymer in organic solar cells (OSCs) in combination
with non-fullerene acceptors. Despite the amorphous nature of the
polymer film, single-junction OSCs with PTPTz–IDT:Y6 as the
active layer achieved a power conversion efficiency of 10.4% (J
SC = 19.8 mA cm–2; V
OC = 0.80 V; fill factor = 0.66), which is the
highest value reported for a single-junction OSC with IDT-based donor
polymers. This work demonstrates that TPTz is a promising electron-acceptor
unit for developing functional polymers with zigzag structures.