Zinc oxide/tin oxide nanoflower-based asymmetric supercapacitors for enhanced energy storage devices

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Abstract

Research on energy storage devices has focused on improving asymmetric supercapacitors (ASCs) by utilizing two different electrode materials. In this work, we have successfully prepared a unique material, ZnO/SnO2 nanoflower, via the hydrothermal method. Graphene oxide (GO) was synthesized by applying the modified Hummers' technique. The ZnO/SnO2 nanoflower was deposited on a polypyrrole (PPY) nanotube/graphene oxide composite (ZS/GP) in two steps: in situ chemical polymerization, followed by a hydrothermal method. Electrochemical properties of the prepared material nanocomposite were analyzed by applying cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) techniques. An asymmetric supercapacitor (ASC) was constructed using ZS/GP nanocomposite as the positive electrode and Caesalpinia pod-based carbonaceous material as the negative electrode material, and its performance was investigated. As a result, the fabricated ASCs were found to have an excellent specific capacitance of 165.88 F g−1 at 1.4 V, with an energy density of 5.12 W h kg−1 and a power density of 2672 W kg−1. The prepared nanocomposite material for the ASC showed a cycle stability of 17k cycles at a current density of 5 A g−1. This study revealed that the electrode material ZS/GP nanocomposite is highly suitable for supercapacitor applications. The ASC device's extended cycle life experiments for 17k cycles produced a coulombic efficiency of 97% and a capacitance retention of 73%, demonstrating the promising potential of the electrode materials for greener as well as efficient energy storage applications while converting abundant bio waste into effective energy.

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APA

Molahalli, V., Soman, G., Bhat, V. S., Shetty, A., Alodhayb, A., & Hegde, G. (2024). Zinc oxide/tin oxide nanoflower-based asymmetric supercapacitors for enhanced energy storage devices. RSC Advances, 14(44), 32314–32326. https://doi.org/10.1039/d4ra05340k

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