Alcohol-Soluble Zwitterionic 4-(Dimethyl(pyridin-2-yl)ammonio)butane-1-sulfonate Small Molecule as a Cathode Modifier for Nonfullerene Acceptor-Based Organic Solar Cells.

A new zwitterionic small molecule 4-(dimethyl(pyridin-2-yl)ammonio)butane-1-sulfonate (PAS), synthesized from 2-dimethylaminopyrindine (2-DMAP), was developed for the ITO cathode modifier. PAS and 2-DMAP dissolved in methanol can form a thin layer on ITO cathode by a simple spin-coating process. The heteroatom moieties in 2-DMAP (sp and sp nitrogen) and PAS (sp nitrogen and sulfonate ion) can coordinate to the ITO surface and decrease the ITO work function by the induced surface dipoles.

Synthesis of side-chain regioregular and main-chain alternating poly(bichalcogenophene)s and an ABC-type periodic poly(terchalcogenophene).

Three unsymmetrical diiodobichalcogenophenes , , and and a diiodoterchalcogenophene were prepared. Grignard metathesis of , , , and occurred regioselectively at the lighter chalcogenophene site because of its relatively lower electron density and less steric bulk. Nickel-catalyzed Kumada catalyst-transfer polycondensation of these Mg species provided a new class of side-chain regioregular and main-chain AB-type alternating poly(bichalcogenophene)s-, , and -through a chain-growth mechanism.

Naphthobisthiadiazole-Based Selenophene-Incorporated Quarterchalcogenophene Copolymers for Field-Effect Transistors and Polymer Solar Cells.

In this research, we developed six new selenophene-incorporated naphthobisthiadiazole-based donor-acceptor polymers PNT2Th2Se-OD, PNT2Se2Th-OD, PNT4Se-OD, PNT2Th2Se-DT, PNT2Se2Th-DT, and PNT4Se-DT. The structure-property relationships have been systematically established through the comparison of their structural variations: (1) isomeric biselenophene/bithiophene arrangement between PNT2Th2Se and PNT2Se2Th polymers, (2) biselenophene/bithiophene and quarterselenophene donor units between PNT2Th2Se/PNT2Se2Th and PNT4Se polymers, and (3) side-chain modification between the 2-octyldodecylthiophene (OD)- and 2-decyltetradecyl (DT)-series polymers. The incorporation of selenophene units in the copolymers induces stronger charge transfer to improve the light-harvesting capability while maintaining the strong intermolecular interactions to preserve the intrinsic crystallinity for high carrier mobility.