Horizontally-oriented barium titanate@polydomine/polyimide nanocomposite films for high-temperature energy storage.

Design idea diagram of the BT@PDA/PI nanocomposite film. [Display omitted] • The scale-like barium titanate (BT) ceramic fillers were prepared from the layered K 0.8 Li 0.27 Ti 1.73 O 4 crystals using solid-phase and hydrothermal processes. • The scale-like BT@Polydomine (PDA) nanoparticles were horizontally ordered distribution in the polyimide (PI) matrix using orientation engineering. • The horizontally ordered BT@PDA can increase the tortuosity of the breakdown path and construct effective conduction barriers, restricting the charges migration and the electron trees growth. • Horizontally ordered BT@PDA/PI nanocomposite films show the highest energy storage density and efficiency comparing with the other BT/PI in past reports. High-temperature ceramics polymer dielectric nanocomposite materials have broad application prospects in energy storage. The barium titanate (BT) plays an important role as one of outstanding representative ceramics in the dielectric nanocomposite materials. However, there is little known for the effects of two-dimensional (2D) BT morphology and layout on the properties of high-temperature nanocomposite materials. Hence, 2D scale-like BT ceramic fillers were prepared from layered K 0.8 Li 0.27 Ti 1.73 O 4 crystals as precursors using a combined solid-state and hydrothermal process. 2D scale-like BT@polydopamine (PDA) core-shell nanocomposites were prepared via coating PDA on the BT. BT@PDA/polyimide(PI) nanocomposite films were fabricated by horizontally oriented distribution of BT@PDA in the PI matrix. The BT@PDA/PI nanocomposite films exhibit a high energy density (3.34 J/cm3) and high charge-discharge efficiency (83.68 %) at 150 °C. It is currently the highest energy storage performance in the BT/PI nanocomposite films at 150 °C. The excellent properties are due to preventing upward breakdown of electrical pathways and promoting dispersion and entanglement of the electrical pathway routes. Additionally, strong electrostatic interactions between the different polymer chains (PDA and PI) restricts the movement of space charges. This work demonstrates that introducing horizontally oriented, organically shell-modified and 2D small-sized BT nanoparticles into a PI matrix is an effective method for improving energy storage performance. [ABSTRACT FROM AUTHOR]