Journal
SURFACE & COATINGS TECHNOLOGY
Volume 410, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.surfcoat.2021.126933
Keywords
Nickel-cobalt oxide; Nickel-cobalt sulfide; Supercapacitor; Water-splitting; Electrocatalysts
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With advancements in technology, the demand for green energy production and storage has been increasing annually. Supercapacitors, particularly those utilizing nickel and cobalt-based materials, have shown significant potential for energy storage applications like water splitting and urea oxidation reaction. The conversion from nickel-cobalt oxide to nickel-cobalt sulfide has demonstrated enhanced energy storage capacity and improved electrochemical properties, showcasing promising outcomes for sustainable energy solutions.
With the advancement in technology, the demand for green energy production and storage is increasing year by year. To meet the increasing demand for green energy, there has been continuous research in a bid to find better materials and efficient ways to store energy. Supercapacitors continue to show a promising green energy storage capacity with their modified and improved electrode materials, which show better electrochemical properties. Transition metals such as Fe, Mo, Ni, etc. based materials have shown great potential for electrode materials in supercapacitors, electrocatalysts for water splitting, and urea oxidation reaction (UOR). In this work, nanostructured nickel-cobalt oxide and nickel-cobalt sulfide were synthesized using a facile hydrothermal method for their applications in a supercapacitor, water splitting, and urea oxidation reaction. It was observed that the properties of nickel-cobalt oxide improved significantly after converting it to nickel-cobalt sulfide. The energy storage capacity of nickel-cobalt sulfide was significantly enhanced compared to nickel-cobalt oxide. Additionally, nickel-cobalt sulfide showed an overpotential of 282 mV, while nickel-cobalt oxide displayed an overpotential of 379 mV to generate a current density of 10 mA/cm(2), towards oxygen evolution reaction. After the introduction of 0.33 M urea, the potential for oxidation of urea for both nickel-cobalt oxide and nickel-cobalt sulfide was reduced significantly.
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