Abstract
Layered intercalating V(2)O(5) (vanadium pentoxide) is a durable battery-type electrode material exploited in supercapacitors. The advancement of V(2)O(5) nanomaterials synthesized from non-aqueous organic solvents holds significant potential for energy storage applications. Liquid-phase synthesis of orthorhombic V(2)O(5) cathode material corroborated its compatibility with quartet glycols and allowed examination of their explicit roles in faradic charge storage efficacy. V(2)O(5) was found to be an intercalative material in all the quartet glycols. The crystalline, rod-like morphology and monodisperse V(2)O(5) electrode were ascribed to the effects of ethylene, diethylene, triethylene, and tetraethylene glycols. Notable differences were observed in the electrochemical analysis of the prepared V(2)O(5) (EV, DV, TV, and TTV). In a three-electrode cell setup, the DV electrode demonstrated a superior specific capacity of 460.2 C/g at a current density of 1 A/g. From the Trasatti analysis, the DV electrode exhibited 961.53 C/g of total capacitance, comprising a diffusion-controlled contribution of 898.19 C/g and a surface-controlled contribution of 63.34 C/g. The aqueous asymmetric device DV//AC exhibited a maximum energy density of 65.72 Wh/kg at a power density of 1199.97 W/kg. The glycol-derived electrodes were anticipated to bepromising materials for supercapacitors and have the potential to meet electrochemical energy needs.