The ever-increasing demand for flexible electronics calls for the development of low-voltage and high-mobility organic thin-film transistors (OTFTs) that can be integrated into emerging display and labeling technologies. Polymer dielectrics with comprehensive and balanced dielectric properties (i.e., a good balance between their insulating characteristics and compatibility with organic semiconductors) are considered particularly important for this end. Here, we introduce a simple but highly efficient strategy to realize this target by using a new type of copolymer as dielectrics. Benefiting from both high chain packing density guaranteeing dielectric properties and surface polarity optimizing molecular packing of organic semiconductors, this rationally designed copolymer dielectric endows flexible OTFTs with high mobility (5.6 cm2 V−1 s−1), low operating voltage (3 V) and outstanding stability. Further, their applicability in integrated circuits is verified. The excellent device performance shows exciting prospects of this molecular-scale engineered copolymer for the realization of plastic high-performance integrated electronics.

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Development of nonflammable separators with excellent properties is in urgent need by next-generation advanced and safe energy storage devices. However, it has been extremely challenging to simultaneously achieve fire resistance, high mechanical strength, good thermomechanical stability, and low ion-transport resistance for polymeric separators. Herein, to address all these needs, we report an in situ formed silica@silica-imbedded polyimide (in situ SiO2@(PI/SiO2)) nanofabric as a new high-performance inorganic–organic hybrid separator. Different from conventional ceramics-modified separators, this in situ SiO2@(PI/SiO2) hybrid separator is realized for the first time via an inverse in situ hydrolysis process. Benefiting from the in situ formed silica nanoshell, the in situ SiO2@(PI/SiO2) hybrid separator shows the highest tensile strength of 42 MPa among all reported nanofiber-based separators, excellent wettability to the electrolyte, good thermomechanical stability at 300 °C, and fire resistance. The LiFePO4 half-cell assembled with this hybrid separator showed a high capacity of 139 mAh·g–1@5C, which is much higher than that of the battery with the pristine PI separator (126.2 mAh·g–1@5C) and Celgard-2400 separator (95.1 mAh·g–1@5C). More importantly, the battery showed excellent cycling stability with no capacity decay over 100 cycles at the high temperature of 120 °C. This study provides a novel method for the fabrication of high-performance and nonflammable polymeric–inorganic hybrid battery separators.

This paper reports our works on the preparation of the silver-nanoparticle-incorporated ultrafine polyimide (PI) ultrafine fibers via a direct ion exchange self-metallization technique using silver ammonia complex cation ([Ag(NH(3))(2)](+)) as the silver precursor and pyromellitic dianhydride (PMDA)/4,4'-oxidianiline (4,4'-ODA) polyimide as the matrix. The polyimide precursor, poly(amic acid) (PAA), was synthesized and then electrospun into ultrafine fibers. By thermally treating the silver(I)-doped PAA ultrafine fibers, where the silver(I) ions were loaded through the ion exchange reactions of the carboxylic acid groups of the PAA macromolecules with the [Ag(NH(3))(2)](+) cations in an aqueous solution, ultrafine polyimide fibers embedded with silver nanoparticles with diameters less than 20 nm were successfully fabricated. The fiber-electrospinning process, the ion exchange process, and various factors influencing the hybrid ultrafine fibers preparation process such as the thermal treatment atmospheres and the thermal catalytic oxidative degradation effect of the reduced silver nanoparticles were discussed. The ultrafine fibers were characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), inductively coupled plasma atomic emission spectroscopy (ICP-AES), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA).