To obtain symmetric supercapacitors (SCs) with high energy density, it is critical to fabricate an electrode with wide potential window and excellent capacitive performance. Herein, by using the strong double hydrolysis reaction between anions and cations, the FeOOH nanosheets on the surface of activated carbon cloth (FeOOH@AC) are prepared through a simple hydrothermal process. The FeOOH@AC electrode exhibits maximum capacitance of 4,090 mF·cm^-2 at wider potential window -1-0 V and 3,250 mF·cm^-2 at 0-1 V versus SCE in 2 M LiNO₃ electrolyte. With two pieces of FeOOH@AC electrodes the obtained symmetric SC can operate at the voltage window of 2 V. This FeOOH symmetric SC shows high energy density of 13.261 mWh·cm^-3 at a power density of 14.824 mW·cm^-3 and maintains 4.175 mWh·cm^-3 at a maximum power density of 118.564 mW·cm^-3, as well as excellent charge storage capacity and cyclic stability. Li ion adsorption and diffusion mechanism on the (200) facets of FeOOH are explained by the density functional theory (DFT) calculations. The simple synthesis process and excellent capacitance performance of the FeOOH@AC composite make it a very promising candidate for high performance symmetric SC electrodes.

Polydimethylsiloxane (PDMS) is an excellent material for investigating the mechanism of triboelectricity as it can easily be used to construct various microstructures. In this study, micro-capacitors (MCs) and variable micro- capacitors (VMCs) were embedded in PDMS by filling PDMS with silver nanoparticles (NPs) and constructing an internal cellular structure. The output performance of the triboelectric nanogenerators (TENGs) based on MCs@PDMS and VMCs@PDMS films was systematically investigated, with variation of the filling content of silver NPs and the pore ratio and size. The microstructure, permittivity, dielectric loss, and capacitance of the VMCs@PDMS films were well characterized. The output current of the TENG based on the VMCs@PDMS film was respectively 4.0 and 1.6 times higher than that of the TENGs based on the pure PDMS film and MCs@PDMS film, and the output power density of the former reached 6 W·m^–2. This study sheds light on the physical nature of conductive nanoparticle fillings and cellular structures in dielectric triboelectric polymers.