Polyvinylpyrrolidone-Functionalized NiCo2O4 Electrodes for Advanced Asymmetric Supercapacitor Application

Abstract

Designing advanced electrode architectures with tailored morphology and redox synergy is essential for achieving high-performance supercapacitive energy storage. In this study, a PVP-assisted hydrothermal approach was employed to synthesize binder-free NiCo2O4 nanostructured electrodes directly on nickel foam substrates. By modulating the PVP concentration (0.5-2 wt%), hierarchical flower-like nanosheets were engineered, with the NiCo-P-1 sample (1 wt% PVP) exhibiting an optimized structure, superior electroactive surface area, and enhanced ion accessibility. Comprehensive electrochemical analysis revealed that NiCo-P-1 delivered an outstanding areal capacitance of 36.5 F/cm(2) at 10 mA/cm(2), along with excellent cycling stability over 15,000 cycles with 80.97% retention. Kinetic studies confirmed dominant diffusion-controlled redox behavior with high OH- diffusion coefficients and minimal polarization. An asymmetric pouch-type supercapacitor device (NiCo-P-1//AC) exhibited a wide operating window of 1.5 V, achieving a remarkable areal capacitance of 187 mF/cm(2), energy density of 0.058 mWh/cm(2), and capacitive retention of 78.78% after 5000 cycles. The superior performance is attributed to the synergistic integration of mixed-valence Ni and Co species, engineered nanosheet morphology, and low interfacial resistance. This work underscores the significance of surfactant-directed design in advancing cost-effective, high-performance electrodes for next-generation flexible energy storage technologies.