Polymer solar cells, with the assistance of nonfullerene
acceptors
(NFAs) and ternary blend strategies, have exceeded 18% power conversion
efficiency. However, most NFA-based ternary blends are constructed
using the strategies developed for polymer–fullerene systems,
and intrinsic properties of these NFAs have been overlooked when designing
a ternary organic solar cell. Here, using a new NFA 2,2′-((4,4,9,9-tetrahexyl-4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-2,7-diyl)
bis(methaneylylidene)) bis(1H-indene-1,3(2H)-dione), referred to IDID,
as the third component, we observed the appearance of a polymorph
of IDID when it was introduced into a PTQ10: PC61BM binary
blend and this ternary blend solar cell showed a significant improvement
in efficiency from 3.38% to 6.04%. This relative increase (with respect
to the best binary cell) is nearly 80% which is the highest among
all the reported organic ternary blends to the best of our knowledge.
Specifically, IDID was found to be nucleated by the host polymer donor
PTQ10 under the assistance of the processing solvent to form a distinct
polymorph, as proven by grazing incidence X-ray diffraction (GIXRD),
differential scanning calorimetry (DSC), and supported by surface
energy measurements. More interestingly, IDID, as a third component
in the PTQ10: PC61BM system, was found to outperform the
structurally similar NFA IDIC, which only boosted the efficiency from
3.38% to 3.55% in ternary polymer solar cells. This work highlights
polymer-mediated polymorphism in NFAs as an important consideration
in selection of components for and the optimization of ternary organic
solar cells.