Wenjun Gan

An ultra-low dielectric porous polyimide film with ε′ ∼1.6@1 MHz was fabricated by an NIPS method. FAS-grafted carbon nitride nanosheets endowed the porous film with advanced hydrophobicity and thermomechanical properties.

Silicon, an attractive anode material, suffers fast capacity fading due to the electrical isolation from massive volumetric expansion upon cycling. However, it holds a high theoretical capacity and low operation voltage in its practical application. In this study, a new water-based binder, MXene clay/hollow core-shell acrylate composite, was synthesized through an in situ emulsion polymerization technique to alleviate the fast capacity fading of the silicon anode efficiently. The efficient introduction of conductive MXene clay and the hollow core-shell structure, favorable to electron and ion transport in silicon-based electrodes, gives a novel conceptual design of the binder material. Such a strategy could alleviate electrical isolation after cycling and promises better electrochemical performance of the high-capacity anodes. The effect of the MXene introduction and hollow core-shell on the binder performance is thoroughly investigated using various characterization tools by comparison with no MXene-containing, core-shell acrylate, and commercial styrene-butadiene latex binders. Consequently, the silicon-based electrode containing the MXene clay/hollow core-shell acrylate binder exhibits a high capacity retention of 1351 mAh g^-1 at 0.5C after 100 cycles and good rate capability of over 1100 mAh g^-1 at 5C.

Herein, an effective technique of curing reaction-induced phase separation (CRIPS) was used to construct a reduced graphene oxide (RGO) network in the immiscible diglycidyl ether of the bisphenol A/polyetherimide (DGEBA/PEI) polyblend system. The unique chemical reduction of RGO facilitated the reduction of oxygenated groups and simultaneously appended amino groups that stimulate the curing process. The selective interfacial localization of RGO was predicted numerically by the harmonic and geometric mean technique and further confirmed by field emission transmission electron microscopy (FETEM) analysis. Due to interfacial localization, the electrical conductivity was increased to 366 S/m with 3 wt.% RGO reinforcement. The thermomechanical properties of nanocomposites were determined by dynamic mechanical analysis (DMA). The storage modulus of 3 wt.% RGO-reinforced polyblend exhibited an improvement of ~15%, and glass transition temperature (T_g) was 10.1 °C higher over neat DGEBA. Furthermore, the total shielding effectiveness (SE_T) was increased to 25.8 dB in the X-band region, with only 3 wt.% RGO, which represents ~99.9% shielding efficiency. These phase separation-controlled nanocomposites with selective localization of electrically conductive nanofiller at a low concentration will extend the applicability of polyblends to multifunctional structural nanocomposite applications.

A tertiary component with higher molecular weight of epoxy terminated polysiloxane (DMS-E11) was incorporated into the diglycidyl ether of bisphenol-A (DGEBA)/thermoplastic polyetherimide (PEI) blends. In this ternary DGEBA/PEI/DMS-E11 system, 25 or 30 wt% PEI and no more than 20 wt% DMS-E11 were used to ensure the formation of a continuous PEI-rich phase via reaction induced phase separation for optimum mechanical properties of blends. The results of morphology monitoring by OM and TRLS indicated that the addition of DMS-E11 could accelerate phase separation of DGEBA/PEI. Obvious differences were observed by SEM/EDS in the final morphologies of the blends. DMS-E11 localized in the PEI-rich phase continuously while it separated with DGEBA into spherical particles in the DGEBA-rich phase. DMA measurements found that the storage modulus and T_g decreased with DMS-E11 content but were compensated partly by the presence of PEI. The results of tensile tests confirmed the synergistic strengthening for epoxy resin from PEI and DMS-E11.