Search

Summary A series of readily accessible and scalable benzo[1,2-b:4,5-b′]dithiophene (BDT)-2,5-dithienyl-thieno[3,4-c]pyrrole-4,6-dione (TPD-T2)-based donor polymers are utilized in organic photovoltaic (OPV) cells blended with the non-fullerene acceptor IT-4F. All polymers readily dissolve in chlorine-free solvents such as xylene, and the corresponding photoactive blend films can be processed in ambient from this solvent to fabricate cells with power conversion efficiencies (PCEs) >12%–14%. Furthermore, the blend processing and OPV metrics are remarkably insensitive to the processing methodology (spin coating versus blade coating), processing solvent, polymer molecular mass and dispersity index, and the results were rationalized by UV-vis, PL, fsTA, AFM, TEM, GIWAXS, and SCLC measurements. These properties enable the first OPV modules, processed in ambient from a benign solvent, with a certified PCE of 10.1% for an area of 20.4 cm2 and >7% after light soaking. The same module also delivers a power of ∼40 μW/cm2 (PCE ∼22%) under indoor lighting.

In this research, a haptacyclic carbazole-based dithienocyclopentacarbazole (DTCC) ladder-type structure was formylated to couple with two 1,1-dicyanomethylene-3-indanone (IC) moieties, forming a new nonfullerene acceptor DTCCIC-C17 using a bulky branched 1-octylnonayl side chain at the nitrogen of the embedded carbazole and four 4-octylphenyl groups at the sp3-carbon bridges. The rigid and coplanar main-chain backbone of the DTCC core provides a broad light-absorbing window and a higher-lying LUMO energy level, whereas the bulky flanked side chains reduce intermolecular interactions, making DTCCIC-C17 amorphous with excellent solution processability. The DTCCIC-C17 as an acceptor is combined with a medium band gap polymer poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b′]dithiophene))-alt-(5,5-(1′,3′-di-2-thienyl-5′,7′-bis(2-ethylhexyl)benzo[1′,2′-c:4′,5′-c′]dithiophene-4,8-dione))] (PBDB-T) as the donor in the active layer to obtain suitable highest occupied molecular orbital/lowest u...

An A–D–A oligomer, DTS(F2BT)2, was synthesized; its structural evolution was studied with DSC, POM, 2D-WAXD, and in-situ GI-XRD. The structural evolution of DTS(F2BT)2 is stepwise and kinetically slow. Both rapid drying and the presence of PC71BM trapped DTS(F2BT)2 in a less ordered nematic (N) phase. PDMS-assisted crystallization enabled a pristine DTS(F2BT)2 thin film to attain a more ordered equilibrium phase, and enhanced the OFET mobility of DTS(F2BT)2. In OPV devices, DIO additive drove the DTS(F2BT)2 domains in the DTS(F2BT)2:PC71BM blended film from the N phase toward the equilibrium phase, and resulted in enhanced OPV performances. These results reveal the slow ordering process of the A–D–A oligomer, and the importance of monitoring the degree of structural evolution of the active thin films in organic optoelectronics.