Spinel ferrites MFe2O4 (M = Co, Cu, Zn) for photocatalysis: theoretical and experimental insights

Abstract

Spinel ferrites exhibit significant promise in photocatalysis and other applications due to their compositional diversity and favourable electronic structure, magnetism, and partially tuneable cation distribution. However, their complex properties, for example, the different behaviour of bulk and nanostructured materials, are not well understood. Here, we combine advanced computational and experimental methods with reactivity measurements to explore the inversion degrees, electronic structures, and photocatalytic activities of MFe₂O₄ spinels (M = Co, Cu, Zn). X-ray diffraction and anomalous X-ray scattering measurements determined bulk inversion degrees of 0.81, 0.91, and 0.26 for CoFe₂O₄, CuFe₂O₄, and ZnFe₂O₄, respectively. Photocatalytic tests showed that only ZnFe₂O₄ is active in the oxygen evolution reaction (OER), which correlates with its favourable band alignment, as determined through electronic structure simulations. Surface-sensitive X-ray Absorption Spectroscopy (XAS) measurements provided insights into the cation distributions at the surfaces, showing significant deviations from bulk properties, particularly in ZnFe₂O₄ in which 52% of the near-surface tetrahedral sites are occupied by Fe cations, compared to 26% in the bulk. DFT simulations of ZnFe₂O₄ illustrated how the surface terminations can alter the thermodynamic preference for cation distribution in comparison with the bulk. Our findings illustrate the complex interplay between surface and bulk properties in spinel ferrites.