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Mixed-valence iron oxides

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Cation Ordering and Electron Transfer

Part of the book series: Structure and Bonding ((STRUCTURE,volume 61))

Abstract

Mixed valence has been considered with reference to three model systems: Fe3O4 (magnetite) is a representative of the ferrospinels and the iron oxides with spinel-related structures, Fe1−δO (wüstite) illustrates a system with random defects and clustering, CaFeO3 (a perovskite) illustrates the consequences of strong Fe4+-O-Fe4+ interactions. The influence of counter cations is particularly marked in systems like the spinels Fe2SnO4 and Fe2MoO4; more subtle effects are illustrated by a comparison of CaFeO3 with SrFeO3. The time τh for an electron transfer between cations of different valence has been considered relative to two times: the period ωR −1⋍10−12s of an optical-mode lattice vibration that traps a mobile electron and the time τn for a Mössbauer nuclear excited state to decay to its ground state. The full range of electron-transfer times τh<10−12s to τh>10−8s has been found for both Fe-Fe interactions across shared site edges or faces and Fe-O-Fe interactions across shared site corners. Perturbations of the periodic potential of an iron array by lattice defects or substitutional ions is shown to increase τh. Moreover, electron-lattice interactions were found to induce cooperative Jahn-Teller distortions in some compounds and charge-density waves (CDW) in others. In the mixed-valent compound Fe3O4, electrostatic interactions between mobile ions combine with electron-lattice interactions to produce, with increasing temperature, transitions from ionic ordering (or a static CDW) in the temperature interval 120<T ≲250 to correlated electron jumps below 120K to uncorrelated electron jumps above 250K and from no spin degeneracy below a magnetic-ordering temperature Tc⋍850K to a spin degeneracy above Tc for the minority-spin electrons. Thus the physical properties induced by mixed valence in iron oxides is seen to be complicated by the fact that the mobile electrons may be either localized or itinerant; in fact localized and itinerant 3d electrons may co-exist at the same ion.

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  1. Laboratoire de Chimie du Solide Minéral, Associé au CNRS, Université de Nancy I, Boite Postale 239, F-54506, Vandœuvre les Nancy, Cedex

    C. Gleitzer

  2. Inorganic Chemistry Laboratory, University of Oxford, South Parks Road, OX1 3QR, Oxford, Great Britain

    J. B. Goodenough

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Gleitzer, C., Goodenough, J.B. (1985). Mixed-valence iron oxides. In: Cation Ordering and Electron Transfer. Structure and Bonding, vol 61. Springer, Berlin, Heidelberg. https://doi.org/10.1007/BFb0111192

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