The TNiFe-P@NC presented excellent HER performance with an overpotential of 40 mV at 10 mA cm −2 and excellent stability in KOH solution. An assembled NiFe-P@NC||NiFe-P@NC electrolyzer could drive 100/500 mA cm −2 in alkaline seawater electrolyte at 1.77/1.93 V.
Economical, efficient and stable transition-metal electrocatalysts are considered great candidatures for replacing noble-metal materials for alkaline hydrogen production. Hence, corrosion engineering and mild phosphating processes were adopted to construct NiFe phosphide encapsulated in nitrogen-doped carbon (NiFe-P@NC). The latter presented a hierarchical morphology with an interconnected three-dimensional porous structure. The unique NiFe-P@NC presented excellent hydrogen evolution reaction (HER) performance with an overpotential of 40 mV at 10 mA cm −2 along with excellent stability in KOH solution (1 M). Notably, NiFe-P@NC required low overpotentials of 149 mV and 280 mV to afford 100 mA cm −2 for HER and oxygen evolution reaction (OER) performance in KOH (1 M) + seawater electrolyte, respectively. Furthermore, as a remarkable bifunctional electrocatalyst, the assembled NiFe-P@NC || NiFe-P@NC electrolyzer with low cell voltages of 1.77 V and 1.93 V could drive 100 mA cm −2 and 500 mA cm −2 in alkaline seawater electrolyte. Remarkably, a water-splitting device could be actuated efficiently by sustainable energies to facilitate a source of hydrogen energy.