Built-In Electric Field and Oxygen Vacancies Synergistically Enhance NiCo-LDH/CeO2 Bifunctional Catalyst.

Abstract

The development of bifunctional electrocatalysts for urea oxidation and oxygen evolution is crucial for stable anodic reactions and efficient cathodic hydrogen production. Herein, a NiCo- (including the 1 μm-scale SEM image in (f))LDH/CeO2 heterostructure catalyst is constructed on nickel foam via two-step electrodeposition. The optimized catalyst exhibits remarkable bifunctional activity. At 100 mA cm-2, the overpotentials are 329 mV for oxygen evolution and 139 mV for urea oxidation. The assembled water-splitting device achieves 500 mA cm-2 at 1.83 V in 1 M KOH. This voltage decreases by 100 mV upon adding 0.33 M urea, with 200 h stability. Mechanistic studies reveal that energy band mismatch induces a built-in electric field. This drives electron transfer from NiCo-LDH to CeO2 and promotes surface reconstruction into highly active NiCoOOH species. CeO2 introduction also significantly increases oxygen vacancy content, facilitating water activation and enhancing reaction kinetics. This work provides a promising strategy for high-performance LDH-based bifunctional electrocatalysts.