Al-etching-induced defect engineering in NiAl LDHs for promoting multifunctional electrocatalytic oxidations: Water oxidation and urea oxidation

Electrocatalytic water splitting is a promising avenue to produce green hydrogen for future sustainable development. Developing multifunctional catalysts with high-performance toward urea oxidation reaction (UOR) and oxygen evolution reaction (OER) offers a unique approach for simultaneously achieving the degradation of urea- containing wastewater and energy-saving hydrogen production. Ni-based materials are a kind of promising materials for electrocatalysis, since its abundant reserve and tolerance. However, low intrinsic activity and catalytic efficiency hinder its wide application. Here, a defect engineering strategy is developed to create vacancies on NiAl layer double hydroxides (LDHs) catalysts by selectively etching Al ions in strong alkaline solution. The obtained NiAl LDHs with rich defects (D-NiAl LDHs) exhibit good OER performance with overpotential of 264 mV to achieve a current density of 10 mA cm- 2 and a Tafel slope of 39.8 mV dec-1.- 1 . In addition, the D-NiAl LDHs catalysts also show excellent UOR activity using a potential of 1.328 V vs . RHE @ 10 mA cm- 2 in alkaline solution. In comparation to NiAl LDHs, the enhanced performance of D-NiAl LDHs toward oxidation of small-molecule OH-- and urea could be attributed to electronic regulation of defects and a larger electrochemical surface area. Partially replacing the OER with the UOR, the driving voltage of overall water splitting reduces effectively from 1.856 V to 1.688 V at a current of 100 mA cm- 2 .