Influence of Side Chain Interdigitation on Strain and Charge Mobility of Planar Indacenodithiophene Copolymers.
Parker J W SommervilleAlex H BalzerGarrett LecroyLorenzo GuioYunfei WangJonathan W OnoratoNadzeya A KukhtaXiaodan GuAlberto SalleoNatalie StingelinChristine K LuscombePublished in: ACS polymers Au (2022)
Indacenodithiophene (IDT) copolymers are a class of conjugated polymers that have limited long-range order and high hole mobilities, which makes them promising candidates for use in deformable electronic devices. Key to their high hole mobilities is the coplanar monomer repeat units within the backbone. Poly(indacenodithiophene-benzothiadiazole) (PIDT C16 -BT) and poly(indacenodithiophene-thiapyrollodione) (PIDT C16 -TPD C1 ) are two IDT copolymers with planar backbones, but they are brittle at low molecular weight and have unsuitably high elastic moduli. Substitution of the hexadecane (C 16 ) side chains of the IDT monomer with isocane (C 20 ) side chains was performed to generate a new BT-containing IDT copolymer: PIDT C20 -BT. Substitution of the methyl (C 1 ) side chain on the TPD monomer for an octyl (C 8 ) and 6-ethylundecane (C 13B ) afford two new TPD-containing IDT copolymers named PIDT C16 -TPD C8 and PIDT C16 -TPD C13B , respectively. Both PIDT C16 -TPD C8 and PIDT C16 -TPD C13B are relatively well deformable, have a low yield strain, and display significantly reduced elastic moduli. These mechanical properties manifest themselves because the lengthened side chains extending from the TPD-monomer inhibit precise intermolecular ordering. In PIDT C16 -BT, PIDT C20 -BT and PIDT C16 -TPD C1 side chain ordering can occur because the side chains are only present on the IDT subunit, but this results in brittle thin films. In contrast, PIDT C16 -TPD C8 and PIDT C16 -TPD C13B have disordered side chains, which seems to lead to low hole mobilities. These results suggest that disrupting the interdigitation in IDT copolymers through comonomer side chain extension leads to more ductile thin films with lower elastic moduli, but decreased hole mobility because of altered local order in the respective thin films. Our work, thus, highlights the trade-off between molecular packing structure for deformable electronic materials and provides guidance for designing new conjugated polymers for stretchable electronics.