Free-standing high-entropy alloy plate for efficient water oxidation catalysis: structure/composition evolution and implication of high-valence metals

We herein report free-standing FeCoNiCrMo high-entropy alloy (HEA) plate as an excellent oxygen evolution reaction (OER) catalyst with activity and durability superior to benchmarking NiFe layered double hydroxide (LDH). It requires overpotentials of 303 and 372 mV to reach current densities of 100 and 700 mA cm  2, respectively, and maintains its activity for at least 120 h in alkaline media. Its dynamic structural/compositional evolution is uncovered, in which Mo metals are rapidly oxidized and dissolved into electrolyte, provoking the concomitant Cr leakage and leaving behind reconstructed active NiFeCo oxyhydroxide nanostructures on the surface. Its enhanced OER (intrinsic) activity is found to be associated with the absorption of resultant Mo oxoanion (MoO42-) and the persistence of trace Cr atoms in surficial NiFeCo oxyhydroxide phase. This work offers useful insights into the origin of high OER activity of HEA catalysts and also provides a feasible way for massproduction of active OER catalysts.

Automated summary

We report a free-standing FeCoNiCrMo high-entropy alloy (HEA) plate that acts as an excellent oxygen evolution reaction (OER) catalyst, showing higher activity and durability compared to the benchmarking NiFe layered double hydroxide (LDH). The HEA catalyst requires overpotentials of 303 and 372 mV to reach current densities of 100 and 700 mA cm  2, respectively, and maintains its activity for at least 120 hours in alkaline media. The enhanced OER activity of the HEA catalyst is attributed to the absorption of Mo oxoanions and the persistence of trace Cr atoms in the surficial NiFeCo oxyhydroxide phase.