In this work, a non-fused electron acceptor with near-infrared
absorption was introduced into double-cable conjugated polymers for
single-component organic solar cells (SCOSCs). The non-fused electron
acceptor contains a simple thienyl-phenyl-thienyl core with 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile
(IC) as the end group, which was used as the side unit to create double-cable
conjugated polymers. In addition, poly(benzodithiophene) was selected
as the conjugated backbone, in which the number of chlorine (Cl) atoms
was varied to tune the optical and electronic properties. The new
double-cable polymers were successfully applied in SCOSCs, providing
an efficiency of over 8% with a broad photoresponse from 300 to 800
nm. When the number of Cl atoms on the repeat unit was increased from
2 to 3, the open-circuit voltage was enhanced to 1.01 V, yielding
a low voltage loss of 0.59 eV, while the efficiency was reduced to
5.28%. The reduced performance is explained by the increased charge
recombination in this polymer, as observed by transient absorption
spectroscopy. This work reports a set of IC-based NIR double-cable
conjugated polymers, which inspire material design toward more efficient
SCOSCs.