Electrocatalytic Oxidation of Urea and Ethanol on Two-Dimensional Amorphous Nickel Oxide Encapsulated on N-Doped Carbon Nanosheets

Hydrogen production from water electrolysis is of great interest for attaining sustainable clean energy storage and conversion, but the required working voltage (>1.23 V) in water splitting limits its applications in industrial expansion. Therefore, replacing the oxygen evolution reaction (OER) with a more favorable anodic oxidation reaction, which can provide more valuable products and less working voltage, will be of great significance for the upcoming expansion of hydrogen production in industrial applications. In this report, a two-dimensional (2D) amorphous sheet-like nickel oxide encapsulated on the nitrogen-doped carbon (NiO x /CN x ) composite was synthesized for the urea oxidation reaction (UOR) and ethanol oxidation reaction (EOR). Remarkably, the catalyst shows 1.647, 1.378, and 1.354 V vs. reversible hydrogen electrode (RHE) potential at 10 mA/cm 2 current density for OER, UOR, and EOR, respectively, with good stability. The overall water, urea, and ethanol electrolyses of NiO x /CN x were carried out by coupling with commercial Pt/C as a cathode which shows only 1.626, 1.43, and 1.414 V cell potential at 20 mA/cm 2 current density. The catalyst also shows excellent chronopotentiometric and dynamic stability toward all the electrolyses. The high catalytic activity of NiO x /CN x may be attributed to the synergistic interaction between the support and materials, amorphous structure, 2D sheet-like morphology, porous structure, and high electrochemical surface area. This finding shows that NiO x /CN x nanosheets can replace noble metal-based catalysts for efficient anodic oxidation reactions.