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Experimental study demonstrates high activity and durability of binder-free NiFeCo2O4 nanorods in anion exchange membrane water electrolyzers, highlighting viable precious-metal-free anodes.
Platinum‐group‐metal‐free catalysts represent a necessary economic choice for industrial‐scale anion exchange membrane (AEM) electrolyzers. A three‐dimensional binder‐free spinel Ni 1 − x Fe x Co 2 O 4 (x = 0.1–0.4) electrocatalyst is synthesized directly on nickel felt via a urea‐mediated sono‐hydrothermal method. The nanorod‐shaped morphology is chosen to reduce mass‐transfer limitations while maintaining catalyst activity. NiFeCo‐2 (20% Fe) offers the optimal balance of iron content, lattice modification, homogeneous nanorod coverage, and surface area, showing the best oxygen evolution reaction (OER) activity, giving 282 mV overpotential at 10 mA cm − 2 and 53 mV dec − 1 Tafel slope. As the anode in an anion exchange membrane water electrolyzer (AEMWE), NiFeCo‐2 reaches 1.748 V at 1 A cm − 2 , 1.92 V at 2 A cm − 2 , and 2.09 V at 4 A cm − 2 in wet cathode mode, and sustains stable operation through two 72‐h accelerated stress test sequences under both wet and dry cathode feeding. Operation starting in dry cathode mode shows better performance retention than in wet mode. Post‐test electron microscopy and textural analysis confirm that the nanorod catalyst layer remains largely preserved, indicating that the observed voltage increase is consistent with resistance growth rather than catalyst loss. These results highlight binder‐free Ni 1 − x Fe x Co 2 O 4 as a promising, affordable anode for AEM water electrolysis.
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Niyati et al. (2026) studied this question.
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