Non‐fused Nonfullerene Acceptors with an Asymmetric Benzo[1,2‐b:3,4‐b′, 6,5‐b"]trithiophene (BTT) Donor Core and Different AcceptorTerminal Units for Organic Solar Cells.

Here in, we have designed two new unfused non‐fullerene small molecules using asymmetric benzo[1,2‐b:3.4‐b′, 6,5‐b"]trithiophene (BTT) as the central donor core and different terminal units i. e., 2‐(3‐oxo‐2,3‐dihydro‐1H‐inden‐1‐ylidene)malononitrile (NFA‐4) and 1,3‐diethyl‐2‐thioxodi hydropyrimidine‐4,6 (1H,5H)‐dione (NFA‐5) and examined their optical and electrochemical properties. Using a wide band‐gap copolymer D18, organic solar cells (OSCs) based on bulk heterojunction of D18:NFA‐4 and D18:NFA‐5 showed overall power conversion efficiency (PCE) of about 17.07 % and 11.27 %, respectively. The increased PCE for the NFA‐4‐based OSC, compared to NFA‐5 counterpart, is due higher value of short circuit current (JSC), open circuit voltage (VOC), and fill factor (FF). Following the addition of small amount of NFA‐5 to the binary bulk heterojunction D18:NFA‐4, the ternary organic solar cells attained a PCE of 18.05 %, surpassing that of the binary counterparts due to the higher values of which is higher than that for the binary counterparts and attributed to the increased values of JSC, FF, and VOC. The higher value of JSC is linked to the efficient use to excitons transferred from NFA‐5 to NFA‐4 with a greated dipole moment than NFA‐5 and subsequently dissociated into a free charge carrier efficiently. [ABSTRACT FROM AUTHOR]