Manipulating the functionality and structures of π-conjugated polymers utilizing intramolecular noncovalent interactions towards efficient organic photovoltaics

Careful control of electronic properties, structural order, and solubility of pi-conjugated polymers is central to the improvement of organic photovoltaic (OPV) performance. In this work, we designed and synthesized a series of naphthobisthiadiazole-quaterthiophene copolymers by systematically replacing the alkyl groups with ester groups and changing the position of the fluorine groups in the quaterthiophene moiety. These alterations lowered the HOMO and LUMO energy levels and systematically varied the combination of intramolecular noncovalent interactions such as OMIDLINE HORIZONTAL ELLIPSISS and FMIDLINE HORIZONTAL ELLIPSISS interactions in the backbone. More importantly, although the introduction of such noncovalent interactions often lowers the solubility owing to the interlocking of backbone linkages, we found that careful design of the noncovalent interactions afforded polymers with relatively high solubility and high crystallinity at the same time. As a result, the power conversion efficiency of OPV cells that used fullerene (PC61BM) and nonfullerene (Y12) as the acceptor was improved. Our work offers important information for the development of high-performance pi-conjugated polymers for OPVs. We synthesized a series of naphthobisthiadiazole-polymers by systematically introducing the alkyl, ester, and fluorine groups in the quaterthiophene co-unit and studied the effect of noncovalent interactions on physical and photovoltaic properties.