High-entropy oxides (HEOs) are of interest for their
unique physical
and chemical properties. Significant lattice distortions, strain,
and tolerance for high-vacancy concentrations set HEOs apart from
single-metal or mixed-metal oxides. Herein, we synthesized and characterized
the structures and compositions, along with the optical, magnetic,
and electrocatalytic properties, of two families of high-entropy mixed-metal
tungsten and molybdenum oxides, AWO4 and B2Mo3O8, where A and B are 3d transition metals. The
HEOs A6WO4 (A = Mn, Fe, Co, Ni, Cu, and Zn)
and B2
5Mo3O8 (B = Mn,
Fe, Co, Ni, and Zn), as well as all accessible single-metal AWO4 and B2Mo3O8 parent compounds,
were synthesized using high-temperature solid-state methods. X-ray
photoelectron spectroscopy analysis of the surfaces revealed that
the HEOs largely had the metal oxidation states expected from the
bulk chemical formulas, but in some cases they were different than
in the parent compounds. A6WO4 exhibited antiferromagnetic
(AFM) ordering with a Néel temperature of 30 K, which is less
than the average of its AFM parent compounds, and had a narrow band
gap of 0.24 eV, which is much lower than all of its parent compounds.
B2
5Mo3O8 was paramagnetic,
despite the existence of AFM and ferromagnetic ordering in several
of its parent compounds and had no observable band gap, which is analogous
to its parent compounds. Both A6WO4 and B2
5Mo3O8 exhibited superior
catalytic activity relative to the parent compounds for the oxygen
evolution reaction, the oxidation half reaction of overall water splitting,
under alkaline conditions, based on the overpotential required to
reach the benchmark surface area normalized current density. Consistent
with literature predictions of OER durability for ternary tungsten
and molybdenum oxides, A6WO4 and B2
5Mo3O8 also exhibited stable performance
without significant dissolution during 10 h stability experiments
at a constant current.