Annealing core@shell nanoparticles (NPs) yields high-entropy alloy NPs. Owing to their dispersed Pt/Pd content and low elemental diffusivity, they exhibit enhanced electrocatalytic performance and durability for the oxygen reduction reaction.

Metal heteroanionic compounds such as oxynitrides, oxysulfides, and oxyhalides have emerged as promising photocatalysts for water splitting, owing to their reduced band gaps compared to conventional oxides. Nonetheless, many of these compounds undergo self-oxidation of the non-oxide anions by photogenerated holes. Herein, we present new metal oxychloride intergrowths based on Bi4TaO8Cl–Bi2GdO4Cl as stable visible light photocatalysts. These intergrowths were prepared using a halide flux method, with their crystal structures analyzed by Rietveld refinement of powder X-ray diffraction data and high-resolution scanning transmission electron microscopy. These analyses support intergrowth formation. The Ta/Gd molar ratio was systematically varied in the intergrowths to rationalize the effect of charge separation and changes in band structure toward photocatalytic water-splitting activity. Furthermore, these intergrowths are capable of sustained overall water splitting in a Z-scheme with Ru/SrTiO3/Rh as a hydrogen evolution catalyst. The high stability of these intergrowth materials is attributed to O 2p orbitals at the valance band edge rather than Cl 3p orbitals, as discerned from electronic structure calculations. These results provide new strategies for designing durable artificial photosynthetic systems by rational modulation of crystal and electronic structure.

Colloidally prepared core@shell nanoparticles (NPs) were converted to monodisperse high entropy alloy (HEA) NPs by annealing, including quinary, senary, and septenary phases comprised of PdCuPtNi with Co, Ir, Rh, Fe, and/or Ru. Intraparticle heterogeneity, i.e., subdomains within individual NPs with different metal distributions, was observed for NPs containing Ir and Ru, with the phase stabilities of the HEAs studied by atomistic simulations. The quinary HEA NPs were found to be durable catalysts for the oxygen reduction reaction, with all but the PdCuPtNiIr NPs presenting better activities than commercial Pt. Density functional theory (DFT) calculations for PdCuPtNiCo and PdCuPtNiIr surfaces (the two extremes in performance) found agreement with experiment by weighting the adsorption energy contributions by the probabilities of each active site based on their DFT energies. This finding highlights how intraparticle heterogeneity, which we show is likely overlooked in many systems due to analytical limitations, can be leveraged toward efficient catalysis.

Pd-Based nanoparticles are excellent alternatives to the typically used Pt-based materials that catalyze fuel cell reactions.