The effect of A-site substitution on the morphological and electrochemical properties of La1-xSrxMnO3 (x = 0, 0.25, 0.50) perovskites was investigated to evaluate their potential as electrode materials for supercapacitors. X-ray diffraction analysis confirmed the formation of the perovskite structure, with minor peak shifts and distortion of crystal structure induced by Sr substitution. Scanning electron microscopy analysis revealed irregularly shaped particulate morphology across all perovskite compositions. The increasing amount of Sr as in La0.5Sr0.5MnO3 (LSM-50) favored the formation of nanosized particles, and energy dispersive X-ray (EDX) analysis confirmed the presence of all constituent elements; EDX elemental mapping also showed a uniform distribution of all elements in the various perovskite compositions. Among all compositions, La0.75Sr0.25MnO3 (LSM-25) possessed the highest specific capacitance (Csp) of 483 Fg−1 at 1 Ag−1 current density in 3 M KOH electrolyte, as determined by electrochemical analysis. This perovskite material also exhibited a capacitance retention of 87.8% after 5000 charge–discharge cycles. Electrochemical impedance spectroscopy revealed that LSM-25 showed the lowest solution resistance (0.68 Ω*cm2) and charge transfer resistance (1.52 Ω*cm2), indicating strong electrode–electrolyte interaction. Detailed analysis of cyclic voltammetry data revealed that the predominant charge storage mechanism was diffusive in nature, with 88% of the diffusive contribution registered for LSM-25. These findings demonstrate that Sr substitution at the A-site significantly enhances the energy storage performance of LaMnO3, making it a promising candidate for supercapacitor applications.
Rehman et al. (Thu,) studied this question.