Abstract Fine-tuning both material design and electrolyte interactions is crucial in the race to develop next-generation supercapacitors. Here, we unveil a solvothermal route to engineer MnFe2O4 nanoparticles (NPs) with tailored electrochemical properties. Structural and morphological analyses confirm the formation of well-defined MnFe2O4 NPs, primed with abundant electroactive sites for superior charge storage. When tested in 3.5 M KOH, these NPs delivered a specific capacitance of 817 F/g at 2.5 A/g. Comparative studies with LiOH, NaOH, and KOH showed that ionic mobility strongly influences performance with K⁺ enabling fastest ion transport and superior charge storage. XPS analysis confirmed Mn2+ and Fe3+ oxidation states, linking surface chemistry to electrochemical behavior. An asymmetric device with activated carbon as the negative electrode and MnFe2O4 NPs as the positive electrode delivered 320 mF/g at 0.07 A/g, retained 185 mF/g at 0.13 A/g, and achieved an energy density of 87 mWh/kg at a power density of 363 W/kg. The device maintained ~72% of its capacitance after 7500 cycles. These results highlight the combined effect of controlled NP synthesis and electrolyte optimization in achieving stable, high-performance supercapacitors suitable for practical energy storage applications.
Rani et al. (Fri,) studied this question.