Thermal Annealing Effects on Long-lived Fluorenol Room Temperature Phosphorescence for Styrene Detection.

Fluorene derivatives have been widely developed in OLEDs because of its efficient fluorescence quantum efficiency, but for which unique rigid biphenyl planar structure and large conjugated system, we hypothesize that they have a great potential for room temperature phosphorescence (RTP) applications, and confirmed this conjecture by subjecting polyvinyl alcohol (PVA) and phosphors to thermal annealing. The cross-linked structure formed during thermal annealing judiciously modulates the phosphorescence emission characteristics of the fluorenol with the synergistic interaction between PVA and fluorenol. Specifically, the lifetime exhibited a substantial increase from 1352.2 ms to 2874.1 ms, accompanied by a quantum yield augmentation from 4.8% to 11.3%, which substantiate that cross-linked induced by thermal annealing effectively amplifies the phosphorescent intensity and stability of the phosphors, facilitating ultralong phosphorescent emission at ambient conditions. Furthermore, an effective probe based on this film is developed for its highly sensitive, quantitative and immediate detection of volatile organic compounds. This investigation not only proffers a novel paradigm for the development of advanced RTP materials but also imparts insightful considerations for optimizing the performance of polymers in conjunction with functional materials, encompassing bioimaging, sensing, and optoelectronic devices.

Preparation and Properties of Novel Cross-Linked Fluorinated Poly(aryl ether) with Low Dielectric Constant and High Thermal Stability.

Fluorinated poly(aryl ether)s (FPAEs) have attracted much attention due to their high thermal stability, excellent mechanical strength, and low dielectric constant. High-molecular-weight fluorinated poly(aryl ether) containing phenylethynyl (FPAE-PE) is successfully synthesized by nucleophilic substitution between 3-ethynylphenol and FPAE. The cross-linked fluorinated poly(aryl ether) (C-FPAE-PE) is prepared by thermal treatment of FPAE-PE at 300 °C. The thermal stability, dynamic thermomechanical property, and dielectric performance of C-FPAE-PE are systematically studied. C-FPAE-PE has excellent heat resistance with 5% weight loss temperature (Td5% ) at 490 °C in air and high thermomechanical properties with storage modulus retention of 50% at 215 °C. C-FPAE-PE displays low and steady dielectric constant of 2.4 and dielectric loss of 0.004 at 215 °C, exhibiting potential applications in the field of microelectronics, communication technology, and energy storage as high-temperature low dielectric materials.

Dual In Situ Polymerization Strategy Endowing Rapid Ion Transfer Capability of Polymer Electrolyte toward Ni-Rich-Based Lithium Metal Batteries.

Poly(vinylidenefluoride-co-hexafluoropropylene) (PVDF-HFP) is one of the most promising candidate electrolyte matrices for high energy batteries. However, the spherical skeleton structure obtained through the conventional method fails to build continuous Li ion transmission channels due to the slow volatilization of high boiling solvent, leading to inferior cycling performance, especially in a Ni-rich system. Herein, a novel strategy is presented to enrich the Li ion transfer paths and improve the Li ion migration kinetics. The tactic is to prepare cross-linked segments through the PVDF-HFP matrix by adopting free radical polymerization and Li salt induced ring-opening polymerization. Most significantly, the visualization of the structure of as-prepared electrolyte is innovatively realized with the combination of polarization microscopy, transmission electron microscopy, scanning electron microscope-energy dispersive spectroscopy, PVDF-HFP, and cross-linked network form interconnected microstructures. Therefore, poly(glycidyl methacrylate and acrylonitrile)@poly(vinylidene fluoride-hexafluoropropylene) electrolyte presents a high ionic conductivity (1.04 mS cm-1 at 30 °C) and a stable voltage profile for a Li/Li cell after 1200 h. After assembly with a LiNi0.8 Co0.15 Al0.05 O2 cathode, a high discharge specific capacity of 190.3 mAh g-1 is delivered, and the capacity retention reaches 88.2% after 100 cycles. This work provides a promising method for designing high-performance polymer electrolytes for lithium metal batteries.