Nickel-cobalt oxalate as an efficient non-precious electrocatalyst for an improved alkaline oxygen evolution reaction

The quest for developing next-generation non-precious electrocatalysts has risen in recent times. Herein, we have designed and developed a low cost electrocatalyst by a ligand-assisted synthetic strategy in an aqueous medium. An oxalate ligand-assisted non-oxide electrocatalyst was developed by a simple wet-chemical technique for alkaline water oxidation application. The synthetic parameters for the preparation of nickel-cobalt oxalate (Ni_2.5Co₅C₂O₄) were optimized, such as the metal precursor (Ni/Co) ratio, oxalic acid amount, reaction temperature, and time. Microstructural analysis revealed a mesoporous block-like architecture for nickel-cobalt oxalate (Ni_2.5Co₅C₂O₄). The required overpotential of Ni_2.5Co₅C₂O₄ for the alkaline oxygen evolution reaction (OER) was found to be 330 mV for achieving 10 mA cm_geo ^-2, which is superior to that of NiC₂O₄, CoC₂O₄, NiCo₂O₄ and the state-of-the-art RuO₂. The splendid performance of Ni_2.5Co₅C₂O₄ was further verified by its low charge transfer resistance, impressive stability performance, and 87% faradaic efficiency in alkaline medium (pH = 14). The improved electrochemical activity was further attributed to double layer capacitance (C _dl), which indefinitely divulged the inferiority of NiCo₂O₄ compared to Ni_2.5Co₅C₂O₄ for the alkaline oxygen evolution reaction (OER). The obtained proton reaction order (ρ _RHE) was about 0.80, thus indicating the proton decoupled electron transfer (PDET) mechanism for OER in alkaline medium. Post-catalytic investigation revealed the formation of a flake-like porous nanostructure, indicating distinct transformation in morphology during the alkaline OER process. Further, XPS analysis demonstrated complete oxidation of Ni²⁺ and Co²⁺ centres into Ni³⁺ and Co³⁺, respectively under high oxidation potential, thereby indicating active site formation throughout the microstructural network. Additionally, from BET-normalised LSV investigation, the intrinsic activity of Ni_2.5Co₅C₂O₄ was also found to be higher than that of NiCo₂O₄. Finally, Ni_2.5Co₅C₂O₄ delivered a TOF value of around 3.28 × 10^-3 s^-1, which is 5.56 fold that of NiCo₂O₄ for the alkaline OER process. This report highlights the unique benefit of Ni_2.5Co₅C₂O₄ over NiCo₂O₄ for the alkaline OER. The structure-catalytic property relationship was further elucidated using density functional theory (DFT) study. To the best of our knowledge, nickel-cobalt oxalate (Ni_2.5Co₅C₂O₄) was introduced for the first time as a non-precious non-oxide electrocatalyst for alkaline OER application.