Carboxamide and carbamate substituted π-conjugated polymers: the effect of hydrogen bonding on photovoltaic properties

Thiophene-pyrazine-thiophene building blocks with carboxamide or carbamate substituents were synthesized and their crystal structures were compared. The carboxamide substituted building block formed intermolecular hydrogen bonds. It showed a twisted conformation and a herringbone packing in a single crystal. The carbamate substituted building block formed intramolecular resonance-assisted hydrogen bonds (RAHBs) and the hydrogen bonds enabled a co-planar structure, an extended pi-conjugation, and a tight lamellar arrangement in a single crystal. Conjugated polymers based on these two building blocks were also synthesized. The hydrogen bonding caused significant differences in the optical, redox, and photovoltaic properties of the polymers. Solar cells based on the polymers as electron donors and Y6 as the acceptor were studied. The devices based on PC-BDT2 which had the intramolecular hydrogen bonds showed a power conversion efficiency (PCE) of 7.9%, while the devices based on PI-BDT which possessed the intermolecular hydrogen bonds gave a PCE of 0.1%.

Automated summary

Thiophene-pyrazine-thiophene building blocks with carboxamide or carbamate substituents were synthesized and compared in terms of crystal structures. The carboxamide substituent in the building block formed intermolecular hydrogen bonds, resulting in a twisted conformation and herringbone packing. The carbamate substituent formed intramolecular resonance-assisted hydrogen bonds (RAHBs), leading to a co-planar structure, extended pi-conjugation, and tight lamellar arrangement. Conjugated polymers based on these building blocks showed significant differences in optical, redox, and photovoltaic properties, with PC-BDT2 exhibiting a higher power conversion efficiency (PCE) of 7.9% compared to PI-BDT with a PCE of 0.1% due to the presence of intramolecular hydrogen bonds.