Abstract

Molecular ordering and miscibility of donor and acceptor materials play critical roles in developing high‐performance as‐cast polymer solar cells (PSCs). In this work, a highly crystalline nonfullerene small molecular acceptor, namely, C8‐IT‐4F, based on alkylated indacenodithieno[3,2‐b]thiophene as the aromatic core and 2‐(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐inden‐1‐ylidene)malononitrile moieties as end groups, is selected and synthesized. The π–π stacking distance in C8‐IT‐4F film can be tuned from 3.88 Å to a more compact (3.48 Å) state by a film‐formation process and the confinement induced by the preaggregated polymer donor PM7, leading to broadened absorption and fine phase separation in the blend film. The optimal morphology with a framework of preaggregated polymer donor, J‐type face‐on π–π stacked acceptor, and appropriate donor/acceptor miscibility facilitates charge generation and transport and reduces charge recombination. As a result, the best PSC based on the as‐cast PM7:C8‐IT‐4F blend film exhibits power conversion efficiency of 14.3%, with an open‐circuit voltage of 0.82 V, a short‐circuit current density of 22.7 mA cm−2, a fill factor of 77.1%, and good photostability with a stabilized fill factor.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call