TY - JOUR
T1 - Synthesis and Magnetic, Optical, and Electrocatalytic Properties of High-Entropy Mixed-Metal Tungsten and Molybdenum Oxides
AU - Katzbaer, Rowan R.
AU - Vincent, William M.
AU - Mao, Zhiqiang
AU - Schaak, Raymond E.
N1 - Publisher Copyright:
© 2023 American Chemical Society. All rights reserved.
PY - 2023/5/22
Y1 - 2023/5/22
N2 - 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, AWO4and B2Mo3O8, where A and B are 3d transition metals. The HEOs A6WO4(A = Mn, Fe, Co, Ni, Cu, and Zn) and B25Mo3O8(B = Mn, Fe, Co, Ni, and Zn), as well as all accessible single-metal AWO4and B2Mo3O8parent 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. A6WO4exhibited 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. B25Mo3O8was 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 A6WO4and B25Mo3O8exhibited 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, A6WO4and B25Mo3O8also exhibited stable performance without significant dissolution during 10 h stability experiments at a constant current.
AB - 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, AWO4and B2Mo3O8, where A and B are 3d transition metals. The HEOs A6WO4(A = Mn, Fe, Co, Ni, Cu, and Zn) and B25Mo3O8(B = Mn, Fe, Co, Ni, and Zn), as well as all accessible single-metal AWO4and B2Mo3O8parent 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. A6WO4exhibited 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. B25Mo3O8was 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 A6WO4and B25Mo3O8exhibited 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, A6WO4and B25Mo3O8also exhibited stable performance without significant dissolution during 10 h stability experiments at a constant current.
UR - http://www.scopus.com/inward/record.url?scp=85159789881&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85159789881&partnerID=8YFLogxK
U2 - 10.1021/acs.inorgchem.3c00541
DO - 10.1021/acs.inorgchem.3c00541
M3 - Article
C2 - 37163751
AN - SCOPUS:85159789881
SN - 0020-1669
VL - 62
SP - 7843
EP - 7852
JO - Inorganic chemistry
JF - Inorganic chemistry
IS - 20
ER -