RhCu 3D Nanoframe as a Highly Active Electrocatalyst for Oxygen Evolution Reaction under Alkaline Condition.
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ABSTRACT:
SUBMITTER: Park J
PROVIDER: S-EPMC5054855 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description: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 (Ni2.5Co5C2O4) 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 (Ni2.5Co5C2O4). The required overpotential of Ni2.5Co5C2O4 for the alkaline oxygen evolution reaction (OER) was found to be 330 mV for achieving 10 mA cmgeo -2, which is superior to that of NiC2O4, CoC2O4, NiCo2O4 and the state-of-the-art RuO2. The splendid performance of Ni2.5Co5C2O4 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 Ni2.5Co5C2O4 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 Ni2.5Co5C2O4 was also found to be higher than that of NiCo2O4. Finally, Ni2.5Co5C2O4 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 Ni2.5Co5C2O4 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 (Ni2.5Co5C2O4) was introduced for the first time as a non-precious non-oxide electrocatalyst for alkaline OER application.
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