Active Site Implantation for Ni(OH)2 Nanowire Network Achieves Superior Hybrid Seawater Electrolysis at 1 A cm−2 with Record‐Low Cell Voltage

Abstract Direct seawater electrolysis provides a grand blueprint for green hydrogen (H 2 ) technology, while the high energy consumption has severely hindered its industrialization. Herein, a promising active site implantation strategy is reported for Ni(OH) 2 nanowire network electrode on nickel foam substrate by Ru doping (denoted as RuNi(OH) 2 NW 2 /NF), which can act as a dual‐function catalyst for hydrazine oxidation and hydrogen evolution, achieving an ultralow working potential of 114.6 mV to reach 1000 mA cm −2 and a small overpotential of 30 mV at 10 mA cm −2 , respectively. Importantly, using the two‐electrode hydrazine oxidation assisted seawater electrolysis, it can drive a large current density of 500 mA cm −2 at 0.736 V with over 200 h stability. To demonstrate the practicability, a home‐made flow electrolyzer is constructed, which can realize the industry‐level rate of 1 A cm −2 with a record‐low voltage of 1.051 V. Theoretical calculations reveal that the Ru doping activates Ni(OH) 2 by upgrading d ‐band centers, which raises anti‐bonding energy states and thus strengthens the interaction between adsorbates and catalysts. This study not only provides a novel rationale for catalyst design, but also proposes a feasible strategy for direct alkaline seawater splitting toward sustainable, yet energy‐saving H 2 production.