A corrosion-engineered transition metal multi-anionic interface for efficient electrocatalysis toward overall water splitting

Rational design and controllable synthesis of transition metal multi-anionic structures to cooperatively catalyze the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) remain a great challenge due to the requirements of high current density and long-term durability for water splitting. Herein, a self-supported sheet-on-sheet hierarchical interface was synthesized via a facile corrosion engineering strategy, where the Ni3S2 microsheet arrays were pre-grown on nickel foam and they provided abundant surface active sites to grow FeOOH nanosheets vertically. The obtained FeOOH/Ni3S2 heterostructure exhibited well-defined dimensions and intimate interface contact with oxygen and a sulfur anion structure, which can modulate the electronic structure of interfacial active sites. Hence, the optimized FeOOH/Ni3S2 required overpotentials of 345 mV and 269 mV to achieve a current density of 100 mA cm-2 for the HER and the OER, respectively. Moreover, it required a voltage of 1.855 V to achieve overall water splitting at a current density of 100 mA cm-2. The interfacial electronic interaction and multi-anionic hierarchical structure not only facilitate the electron transfer between the FeOOH/Ni3S2 surface and intermediate species but also accelerate the kinetic rate. This paper provides a new avenue to design multi-anionic hierarchical structures as cost-effective and highly stable electrocatalysts for practical overall water splitting. FeOOH/Ni3S2 heterostructure was fabricated via a corrosion engineering strategy, which can steadily catalyze overall water splitting at high current density.

Automated summary

This study successfully synthesized FeOOH/Ni3S2 heterostructure via a corrosion engineering strategy, which features a multi-anionic hierarchical structure and interfacial electronic interaction. The obtained heterostructure can catalyze overall water splitting reaction with low overpotentials at high current density.