Electron-Redistributed NiCo@NiFe-LDH Core–Shell Heterostructure for Significantly Enhancing Electrochemical Water Splitting

Layered double hydroxides (LDHs) are some of the most promising precursors for the development of economically stable and efficient electrocatalysts for water splitting. An effective strategy for designing excellent performance electrocatalysts is to assemble core–shell heterostructures with a tunable electronic structure. In this work, three core–shell heterostructure electrocatalysts (NiCo@NiFe-LDH100/150/200) are developed by a simple hydrothermal and subsequent electrodeposition method on Ni foam. Among them, NiCo@NiFe-LDH150/NF exhibits the best oxygen evolution reaction electrocatalytic activity and long-term stability with a low overpotential of 197 mV to deliver a current density of 10 mA cm–2. In addition, an efficient and stable alkaline electrolytic cell with NiCo@NiFe-LDH150/NF both as the cathode and anode achieves a voltage of 1.66 V at a current density of 10 mA cm–2 and realization of ultralong stability at current densities of 20 and 200 mA cm–2 for 200 h. Density functional theory calculations reveal the strong electron interaction at the heterogeneous interface of the NiCo@NiFe-LDH150/NF core–shell structure, which effectively improves the intrinsic electron conductivity and ion diffusion kinetics and makes an important contribution to the electrocatalytic performance of the material. This work provides a new idea for the selection of materials for electrochemical water splitting by the construction of heterojunction interfaces.