Qian Che, Weifeng Zhang, Jiadi Chen, Chang Cui, Zhihui Chen, Liping Wang, Gui Yu
Two intrinsically flexible conjugated polymers, PBT-90 and PFBT-90, were designed and synthesized via aldol polycondensation. Both polymers incorporate a novel double-flexible-node unit, 5,5'-bis(1,1,2,2-tetrafluoro-2-(thiophen-2-yl)ethyl)-2,2'-bithiophene, which can reduce brittleness and enhance recoverability in both bulk polymers and processed films. Both polymers displayed n-type charge transport in transistors fabricated on a polyethylene terephthalate substrate, achieving high electron mobilities (µe) of 3.85 and 4.56 cm2 V-1 s-1 for PBT-90 and PFBT-90, respectively, only slightly inferior to 5.44 and 6.37 cm2 V-1 s-1 of their fully conjugated analogues, PBT-100 and PFBT-100. Utilizing a self-developed PET/CYTOP/AlOx three-layer thin film transfer process, combined with orthogonal solvent design and interlayer protection strategies, we fabricated high-performance stretchable transistors. The PFBT-90-based devices exhibited a record-high µe of 3.51 cm2 V-1 s-1 in the pristine state. Under 100% strain, they retained a µe > 2.86 cm2 V-1 s-1 (>80% retention). The remarkable device performance originates from its suitable frontier molecular orbitals structure, low backbone glass transition temperature, and well-balanced finitely conjugated backbone, where rigid conjugated segments ensure highly efficient charge carrier transport and flexible nonconjugated segments dissipate stress. Our findings offer a pivotal molecular design strategy and a versatile fabrication process for advanced stretchable organic electronics.