Fabrication of Ultra-Durable and Flexible NiPx-Based Electrode toward High-Efficient Alkaline Seawater Splitting at Industrial Grade Current Density

Designing nonprecious metal-based electrocatalysts to yield sustainable hydrogen energy by large-scale seawater electrolysis is challenging to global emissions of carbon neutrality and carbon peaking. Herein, a series of highly efficient, economical, and robust Ni-P-based nanoballs grown on the flexible and anti-corrosive hydrophobic asbestos (NiPx@HA) is synthesized by electroless plating at 25 degrees C toward alkaline simulated seawater splitting. On the basis of the strong chemical attachment between 2D layered substrate and nickel-rich components, robust hexagonal Ni5P4 crystalline modification, and fast electron transfer capability, the overpotentials during hydrogen/oxygen evolution reaction (HER/OER) are 208 and 392 mV at 200 mA cm(-2), and the chronopotentiometric measurement at 500 mA cm(-2) lasts for over 40 days. Additionally, the versatile strategy is broadly profitable for industrial applications and enables multi-elemental doping (iron/cobalt/molybdenum/boron/tungsten), flexible substrate employment (nickel foam/filter paper/hydrophilic cloth), and scalable synthesis (22 cm x 22 cm). Density functional theory (DFT) also reveals that the optimized performance is due to the fundamental effect of incorporating O-source into Ni5P4. Therefore, this work exhibits a complementary strategy in the construction of NiPx-based electrodes and offers bright opportunities to produce scalable hydrogen effectively and stably in alkaline corrosive electrolytes.

Automated summary

In this study, highly efficient and robust Ni-P-based nanoballs (NiPx@HA) grown on hydrophobic asbestos were synthesized for alkaline simulated seawater electrolysis. The strong chemical attachment between the substrate and nickel-rich components, as well as the hexagonal Ni5P4 crystalline modification and fast electron transfer capability contribute to the excellent performance. The versatile strategy allows for multi-elemental doping, flexible substrate employment, and scalable synthesis.