Abstract
To address the growing demand of highly Ragone efficient electrochemical energy storage devices, we have innovated a synthetic design strategy and employed a tartrate-mediated kinetic precipitation process to fabricate an ultraporous ribbon-like hierarchical microstructure of Ni-, Mn-, and Co-based ternary oxide, i.e., NiO/MnCo2O4, and employed it as a battery-type positive electrode material to assemble an ASSHSC (all-solid-state hybrid supercapacitor) device with nitrogen-doped reduced graphene oxide (N-rGO) as the positive electrode material. NiO/MnCo2O4 exhibits distinct crystallographic phase, near-perfect elemental stoichiometry, evident bulk porosity, and rich nanocrystallite assembly in the randomly arranged microstructure of near-uniform size and shape. Thorough electrochemical studies corroborate that the battery-type NiO/MnCo2O4 exhibits remarkable electrochemical reversibility during charge transfer, high efficiency in supercapacitive charge storage, low charge transfer, series and diffusion resistance. The NiO/MnCo2O4||N-rGO ASSHSC device assembled with the PVA-KOH film as the separator electrolyte offers rich charge storage physiognomies, which accentuates excellent electromicrostructural compatibility between the electrode materials in the device. The NiO/MnCo2O4||N-rGO ASSHSC device shows low charge transfer and diffusion resistance, and it also delivers high mass and areal specific capacitance/capacity, energy and power density, Ragone efficiency (∼131 Wh kg-1 at ∼2134 W kg-1 and ∼31 Wh kg-1 at ∼5005 W kg-1), and extended operational durability (98.2% specific capacitance retention after 12,000 successive GCD cycles) under high-rate working conditions. The present optimized approach to design highly efficient multiple transition-metal-based oxides as battery-type electrode materials and fabricate rich Ragone-efficient ASSHSC devices can be widely adopted in the future development of high-performance hybrid supercapacitors, which may be largely integrated in various pioneering technologies.
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