Hierarchical FeO(OH)-CoCeV (Oxy)hydroxide as a Water Cleavage Promoter

The search for a bifunctional electrocatalyst having water cleavage promoting ability along with the operational stability to efficiently generate oxygen and hydrogen could lead to robust systems for applications. These fundamental ideas can be achieved by designing the morphology, tuning the electronic structure, and using dopants in their higher oxidation states. Herein, we have fabricated a binder-free FeO(OH)-CoCeV-layered triple hydroxide (LTH) bifunctional catalyst by a two-step hydrothermal method, in which the nanograin-shaped FeO-(OH) coupled with CoCeV-LTH nanoflakes provides more electro-catalytically active sites and enhances the charge-transfer kinetics for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The composition-optimized electrocatalyst (FeO-(OH)-Co0.5Ce0.05V0.15-LTH) acts as an efficient water cleavage composite by virtue of its favorable oxidation states leading to cyclic redox couples, which yields an overpotential of 53 mV for HER and 227 mV for OER to drive 10 mA/cm(2) current density in 1 M KOH with a corresponding Tafel slope of 70 mV/dec for HER and 52 mV/dec for OER. Furthermore, for the overall water splitting reaction, the heterostructure FeO(OH)-Co0.5Ce0.05V0.15-LTH acts as a dual-functional electrocatalyst, which requires a cell voltage of 1.52 V versus RHE to drive 10 mA/cm(2) current density.

Automated summary

This study successfully fabricated a bifunctional electrocatalyst with high operational stability for efficient generation of hydrogen and oxygen. By designing the morphology and optimizing the composition, it achieved overpotentials of 53 mV for HER and 227 mV for OER under 10 mA/cm(2) current density in 1 M KOH.