Abstract

Herein, an asymmetric supercapacitor (ASC) device was assembled by employing the pristine CoF2 as active positive electrode material and activated carbon (AC) as negative electrode material. The CoF2 electrode exhibited an outstanding electrochemical behavior with enhanced specific capacitance (Cs) of 872 F/g at 1 A/g current density in three electrode configurations. The reversible Faradaic redox reactions in CoF2 instigate the formation of cobalt-oxyfluorides and generating the mixed valence state of Co (Co2+ and Co3+) which improves its electrical conductivity and electrochemical behaviors. Furthermore, the room temperature paramagnetic nature of CoF2 increases the gradient force of ions which could possibly increase the redox reactions at the electrolyte/electrode interface. The constructed asymmetric device structure of CoF2//AC revealed a quasi-rectangular shaped cyclic voltametric curve and symmetrical semi-triangular shaped galvanostatic charge-discharge profiles, respectively, which affirms the combined electric double layer capacitance and pseudocapacitive nature by its hybrid assembly. Hence, the constructed CoF2//AC ASC demonstrated a remarkable specific capacitance of 141 F/g, energy density of 44.06 Wh.Kg−1, and power density of 422.97 W.Kg−1 at 1 A/g with the high cell voltage of 1.5 V. The CoF2//AC ASC device retained c.a. 92 % of its initial capacitance and attained over 96 % of Coulombic efficiency after 2000 cycles of charge-discharge profiles at 1 A/g, which suggests the high electrochemical stability. This admirable electrochemical performance and the origin towards the magneto-capacitance of CoF2 could pave a new way to explore next generation high-performance supercapacitors.

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