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

Authors :
Hall, Charlotte A.
Ferrer, Pilar
Grinter, David C.
Kumar, Santosh
da Silva, Ivan
Rubio-Zuazo, Juan
Bencok, Peter
de Groot, Frank
Held, Georg
Grau-Crespo, Ricardo
Source :
Journal of Materials Chemistry A; 11/21/2024, Vol. 12 Issue 43, p29645-29656, 12p
Publication Year :
2024

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 MFe<subscript>2</subscript>O<subscript>4</subscript> 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 CoFe<subscript>2</subscript>O<subscript>4</subscript>, CuFe<subscript>2</subscript>O<subscript>4</subscript>, and ZnFe<subscript>2</subscript>O<subscript>4</subscript>, respectively. Photocatalytic tests showed that only ZnFe<subscript>2</subscript>O<subscript>4</subscript> 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 ZnFe<subscript>2</subscript>O<subscript>4</subscript> in which 52% of the near-surface tetrahedral sites are occupied by Fe cations, compared to 26% in the bulk. DFT simulations of ZnFe<subscript>2</subscript>O<subscript>4</subscript> 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20507488
Volume :
12
Issue :
43
Database :
Complementary Index
Journal :
Journal of Materials Chemistry A
Publication Type :
Academic Journal
Accession number :
180716655
Full Text :
https://doi.org/10.1039/d4ta04941a