Lattice-disordered high-entropy metal hydroxide nanosheets as efficient precatalysts for bifunctional electro-oxidation

Electro-oxidation reactions (EORs) are important half reactions in overall and assisted water electrolysis, which are crucial in achieving economic and sustainable hydrogen production and realizing simultaneous wastewater treatment. Current studies indicate that the high-valence metal ions that are locally enriched in the catalysts or generated in situ during the anodic preoxidation process are active species for EORs. Hence, designing (pre)catalysts with enriched local active sites and boosted preoxidation is of great importance. In this work, with a focus on improving the EOR performance toward the oxygen evolution reaction (OER) and the urea oxidation reaction (UOR), we fabricated a lattice-disordered high-entropy FeCuCoNiZn hydroxide nanoarray catalyst that exhibits robust bifunctional OER and UOR behavior. The high-entropy feature could bring in a unique catalytic ensemble effect and remarkably improve the intrinsic OER/UOR activity. The lattice-disordered structure could not only enrich the local high -valence metal ions as active sites but also provide abundant reactive surface sites to accelerate the pre -oxidation process, thus leading to enriched active sites for the OER and UOR. Benefitting from the struc-tural merits, the lattice-disordered high-entropy catalyst exhibits excellent OER and UOR activity with low overpotential, large current density and enhanced intrinsic activity, and no performance degradation but dramatic 35.3% and 88.7% enhancement in activity can be achieved during the long-term OER and UOR tests, respectively. The robust OER and UOR performance makes the lattice-disordered high- entropy catalyst a promising candidate for overall and urea-assisted water electrolysis from industrial, agricultural and sanitary wastewater.(c) 2023 Elsevier Inc. All rights reserved.

Automated summary

A lattice-disordered high-entropy FeCuCoNiZn hydroxide nanoarray catalyst was fabricated, showing robust bifunctional oxygen evolution reaction (OER) and urea oxidation reaction (UOR) behavior. The high-entropy feature and lattice-disordered structure significantly improved the intrinsic activity and enriched the active sites for OER and UOR. The catalyst exhibited excellent OER and UOR activity with low overpotential, large current density, and enhanced intrinsic activity, making it a promising candidate for water electrolysis.