The development of NiCo2O4/PVP/PANI heterogeneous nanocomposites as an advanced battery-type electrode material for high-performing supercapacitor application

超级电容器 纳米复合材料 聚苯胺 材料科学 电极 化学工程 电池(电) 储能 纳米技术 电容 导电聚合物 聚合物 化学 复合材料 量子力学 聚合 物理 工程类 物理化学 功率(物理)
作者
Jihyeon Park,Seungju Jo,Narasimharao Kitchamsetti,Shakir Zaman,Daewon Kim
出处
期刊:Journal of Alloys and Compounds [Elsevier]
卷期号:926: 166815-166815 被引量:22
标识
DOI:10.1016/j.jallcom.2022.166815
摘要

Recently, various electroactive materials composed of binary transition metal oxides (TMOs), and conducting polymers have been extensively studied, with the materials demonstrating great potential in high-performing battery-type electrodes. Furthermore, the development of heterogeneous nanocomposites is a versatile approach because of their well-defined surface morphology and the significant synergistic effect of the various species. In this study, NiCo2O4 (NCO) combined with polyvinyl pyrrolidone (PVP) and polyaniline (PANI) hybrid nanocomposites of NCO/PVP/PANI are newly developed using a facile hydrothermal method. The NCO in combination with PVP and PANI species provides the interconnected hierarchical characteristics by offering large electroactive sites that facilitate the charge transfer. The NCO/PVP/PANI1.5 nanocomposites had a high areal capacity of 698.44 µAh cm−2 at a current density of 4 mA cm–2 and a remarkable capacitance retention of 86 % over 4,000 galvanostatic charge/discharge (GCD) cycles owing to its excellent synergistic effect of the rich faradaic redox reaction kinetics of metallic species, and highly conductive materials. Moreover, the proposed NCO/PVP/PANI1.5 battery-type positive electrode was successfully assembled with an activated carbon negative electrode, resulting a hybrid device with a high energy density of 27.60 Wh kg−1 at a power density of 874.9 W kg−1 and excellent cycling stability. This research holds the significant promise for advanced heterogeneous materials in energy storage systems by describing the newly developed nanocomposites.
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