Demonstrates improved oxygen evolution efficiency in catalytic electrodes, suggesting a new approach for water electrolysis.
Developing low-cost, corrosion-resistant catalytic electrodes for the oxygen evolution reaction (OER) is essential for efficient and durable hydrogen production via anion exchange membrane water electrolysis (AEMWE). Herein, we report a polydopamine (PDA)-coated Fe,Cr codoped NiS 2 self-supporting electrode (PDA-Fe,Cr-NiS 2 @NF). The nitrogen-rich functional groups of PDA establish robust M-N coordination bonds with active metal centers, thereby suppressing metal dissolution during anodic reconstruction. In parallel, the conductive PDA layer regulates interfacial electron redistribution and optimizes the hydrogen-bond network of interfacial water, lowering the OER activation energy. Its conformal protective layer further enhances catalyst stability. The optimized electrode delivers an OER overpotential of only 247 mV at 1 A cm –2 . When integrated as the anode with a PtNiC cathode in an AEMWE cell, the system reaches a current density of 1 A cm –2 at only 1.737 V at 70 °C and operates stably for 1000 h, with a voltage decay rate of only 0.1 mV h –1, an electrolysis efficiency of 71.96%, and an energy consumption of 4.157 kWh Nm 3– H 2 . This work establishes a viable coordination-protection strategy for constructing durable, high-performance OER electrodes for industrial-scale water electrolysis.
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Duan et al. (2026) studied this question.
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