Scalable self-assembly interfacial engineering for high-temperature dielectric energy storage.

Flexible polymer dielectrics which can function well at elevated temperatures continue to be significant in harsh condition energy storage. However, state-of-the-art high-temperature polymers traditionally designed with conjugated structures for better thermal stability have compromised bandgaps and charge injection barriers. Here, we demonstrate a self-assembled polyvinyl alcohol (PVA)/montmorillonite (MMT) coating to impede charge carriers injecting into the polyimide (PI) polymer film. The anisotropic conductivity of the 2D nanolayered coating further dissipates the energy of charges through tortuous injection pathways. With the coating, high field pre-breakdown conduction measurement and space-charge profiling of PI films reveal a clear shifting of the dominant mode of conduction from the bulk-limited hopping to Schottky-injection limited conduction. The coating thus imparts PI films with a significantly suppressed electrical conduction (∼10×), and substantially improved discharge efficiency (7×) and energy density (2.7×) at 150°C. The facile and scalable flow-induced fabrication unleash enormous applications for harsh condition electrification.

Reviving the "Schottky" Barrier for Flexible Polymer Dielectrics with a Superior 2D Nanoassembly Coating.

The organic insulator-metal interface is the most important junction in flexible electronics. The strong band offset of organic insulators over the Fermi level of electrodes should theoretically impart a sufficient impediment for charge injection known as the Schottky barrier. However, defect formation through Anderson localization due to topological disorder in polymers leads to reduced barriers and hence cumbersome devices. A facile nanocoating comprising hundreds of highly oriented organic/inorganic alternating nanolayers is self-coassembled on the surface of polymer films to revive the Schottky barrier. Carrier injection over the enhanced barrier is further shunted by anisotropic 2D conduction. This new interface engineering strategy allows a significant elevation of the operating field for organic insulators by 45% and a 7× improvement in discharge efficiency for Kapton at 150 °C. This superior 2D nanocoating thus provides a defect-tolerant approach for effective reviving of the Schottky barrier, one century after its discovery, broadly applicable for flexible electronics.

An efficient method to prepare aluminosilicate nanoscrolls under mild conditions.

The conventional approach to exfoliate kaolinite to form aluminosilicate nanoscrolls is very time-consuming. Herein, we report a novel method to prepare aluminosilicate nanoscrolls from kaolinite by catalysis of AlCl3 under mild conditions. This method is highly efficient, environmentally friendly, and can be easily scaled up for mass production.

In situ growth of a CaAl-NO3--layered double hydroxide film directly on an aluminum alloy for corrosion resistance.

In this study, a calcium-aluminum-layered double hydroxide (CaAl-LDH) thin film was grown on an AA6082 aluminum alloy, for the very first time, by using a facile in situ growth method in an effort to investigate the CaAl-LDH structural geometry and corresponding corrosion resistance properties. The structure and surface morphologies of the CaAl-LDH thin film were studied using a scanning electron microscope (SEM) equipped with an EDS detector, a transmission electron microscope (TEM), an X-ray diffractometer (XRD), and a Fourier transform infrared spectrometer (FT-IR), while the electron impendence spectra (EIS) and potentiodynamic curves were recorded to understand the LDH anticorrosion behavior. The findings demonstrated that thin, well-developed CaAl-LDH coatings with different surface morphologies can be prepared with eminent corrosion resistance properties. Specifically, the CaAl-LDH thin film synthesized at 140 °C-24 h synthetic conditions showed a large impedance modulus of 7.3 Ω cm2 at 0.01 Hz (|Z|f = 0.01 Hz), along with a low corrosion current density (Icorr) of 0.0007 µA cm-2, while a vertically orientated rod like structure with a uniform surface morphology was observed.

Rheological, Thermal, and Degradation Properties of PLA/PPG Blends.

The work presented herein focuses on simulating the compounding process via a torque rheometer, as well as the relationship between the melt viscosity and the polymer molecular weight (MW). We aim to predict the plasticization of polylactic acid (PLA) using polypropylene glycol (PPG) with different MWs. The rheological properties of the PLA/PPG composites containing PPG with different MWs were systematically studied by capillary rheometry and torque rheometry. The initial degradation of PLA/PPG composites during melt processing was monitored in real time. The results indicate that PPG can significantly reduce the melt viscosity of PLA/PPG composites, leading to obvious pseudoplastic fluid behavior. The lower the MW of PPG, the lower the viscosity of the PLA/PPG composite. The addition of PPG was favorable for the degradation of PLA during processing, and the degradation degree of the composite materials increased as the MW of PPG was decreased.