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Ruthenium modulated Ni-Co pyrophosphate architectures enabling accelerated oxygen evolution in anion exchange membrane electrolyzer

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10.1016/j.mtsust.2026.101380
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The development of efficient and durable electrocatalysts remains crucial for sustainable production of hydrogen via water electrolysis. Herein, we report a ruthenium-modified nickel-cobalt pyrophosphate [(NiCo)(P2O7)] catalyst (Ru-NCP) as a class leading oxygen evolution electrode under alkaline conditions and its application in anion exchange membrane water electrolysis (AEMWE). The NiCo2O4 precursor was transformed into a pyrophosphate framework through phosphidation, followed by Ru deposition and thermal reduction under Ar/H2. Structural analyses (XRD, Raman, TEM, XPS) confirmed the formation of the (NiCo)(P2O7) lattice and Ruinduced modulation of metal oxidation states. Electrochemical studies revealed an overpotential of 1.567 V at 100 mA cm- 2 and stable operation at 400 mA cm- 2 for 24 h in 1.0 M KOH. Integrated into an AEMWE, Ru-NCP achieved 1.6 A cm-2 at 4.5 V with extended durability. The superior performance arises from Ru-mediated electronic reconfiguration and enhanced active site accessibility within the pyrophosphate matrix.

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MATERIALS TODAY SUSTAINABILITY

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2589-2347

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openAccess

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