Abstract
To accomplish an efficient and high-performance flexible supercapattery, electrochemically active materials with multicomponent and rational morphological architectures are highly enviable. Herein, we demonstrate dual-morphology-based mesoporous nickel-ferrite nanoparticles embedded in ultra-thin nanosheets (NiFe2O4-NP-NS) grown directly on a carbon cloth (CC) substrate to develop a free-standing electrode (NiFe2O4-NP-NS@CC) for a flexible supercapattery. Owing to the symmetric effects of bimetallic oxides, porosity with a higher surface area and dual morphological impact, the designed electrode conferred significantly enhanced electrochemical performance in aqueous as well as solid-state electrolytes. The binder-free architecture offered an excellent capacity of 965 C g(-1) (1608 F g(-1)) at 5 mV s(-1) with high coulombic efficiency and a good capacity retention of 94.20% over 5000 cycles, while the single morphology-based electrode showed only 551 C g(-1) (919 F g(-1)) at 5 mV s(-1) with a capacity retention of 90.50% over 5000 cycles under identical conditions. A redox-reaction mechanism is proposed based on ex situ XRD, XPS, and TEM analysis, and it further quantitatively distinguished the pseudocapacitive and diffusion-controlled charge storage proportions of NiFe2O4-NP-NS@CC cathodes in aqueous electrolytes. Additionally, the flexible supercapattery (NiFe2O4-NP-NS@CC//NPC) exhibits an outstanding energy density of 69 W h kg(-1) at a power density of 771 W kg(-1) with highly flexible features, which exceeds that of supercapacitors. These results present the fabricated device as a promising candidate in the field of energy storage.