We have designed a new medium bandgap non-fullerene small-molecule
acceptor consisting of an IDT donor core flanked with 2-(6-oxo-5,6-dihydro-4H-cyclopenta[c]-thiophene-4-ylidene) malononitrile
(TC) acceptor terminal groups (IDT-TC) and compared its
optical and electrochemical properties with the IDT-IC acceptor. IDT-TC showed an absorption profile from 300 to 760 nm, and
it has an optical bandgap of 1.65 eV and HOMO and LUMO energy levels
of −5.55 and −3.83 eV, respectively. In contrast to
IDT-IC, IDT-TC has an upshifted LUMO energy level, which
is advantageous for achieving high open-circuit voltage. Moreover, IDT-TC showed higher crystallinity and high electron mobility
than IDT-IC. Using a wide bandgap D–A copolymer P as the donor,
we compared the photovoltaic performance of IDT-TC, IDT-IC,
and IDT-IC-Cl nonfullerene acceptors (NFAs). Polymer solar cells (PSCs)
using P: IDT-TC, P: IDT-IC, and P:IDT-IC-Cl active layers
achieved a power conversion efficiency (PCE) of 14.26, 11.56, and
13.34%, respectively. As the absorption profiles of IDT-IC-Cl and IDT-TC are complementary to each other, we have incorporated IDT-TC as the guest acceptor in the P: IDT-IC-Cl active layer
to fabricate the ternary (P:IDT-TC: IDT-IC-Cl) PSC, demonstrating
a PCE of 16.44%, which is significantly higher than that of the binary
BHJ devices. The improvement in PCE for ternary PSCs is attributed
to the efficient exploitation of excitons via energy transfer from IDT-TC to IDT-IC-Cl, suitable nanoscale phase separation,
compact stacking distance, and more evenly distributed charge transport.