Electrostatically driven charge-ordering in Fe2OBO3

J. P. Attfield (), A. M. T. Bell, L. M. Rodriguez-Martinez, J. M. Greneche, R. J. Cernik, J. F. Clarke and D. A. Perkins
Additional contact information
J. P. Attfield: University of Cambridge
A. M. T. Bell: University of Cambridge
L. M. Rodriguez-Martinez: University of Cambridge
J. M. Greneche: Laboratoire de Physique de l'Etat Condensé, UPRESA CNRS 6087, Université du Maine
R. J. Cernik: Synchrotron Radiation Source, CLRC Daresbury Laboratory
J. F. Clarke: Chemical Crystallography Laboratory, University of Oxford
D. A. Perkins: Chemical Crystallography Laboratory, University of Oxford

Nature, 1998, vol. 396, issue 6712, 655-658

Abstract: Abstract Charge-ordering is an important phenomenon in conducting metal oxides: it leads to metal–insulator transitions1 in manganite perovskites (which show ‘colossal’ magnetoresistances), and the Verwey2 transition in magnetite (in which the material becomes insulating at low temperatures when the conduction electrons freeze into a regular array). Charge-ordered ‘stripes’ are found in some manganites3,4 and copper oxide superconductors5; in the latter case, dynamic fluctuations of the stripes have been proposed6 as a mechanism of high-temperature superconductivity. But an important unresolved issue is whether the charge-ordering in oxides is driven by electrostatic repulsions between the charges (Wigner crystallization7), or by the strains arising from electron–lattice interactions (such as Jahn–Teller distortions) involving different localized electronic states. Here we report measurements on iron oxoborate, Fe2OBO3, that support the electrostatic repulsion charge-ordering mechanism: the system adopts a charge-ordered state below 317 K, in which Fe2+ and Fe3+ ions are equally distributed over structurally distinct Fesites. In contrast, the isostructural manganese oxoborate, Mn2OBO3, has been previously shown8 to undergo charge-ordering through Jahn–Teller distortions. We therefore conclude that both mechanisms occur within the same structural arrangement.

Date: 1998
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DOI: 10.1038/25309

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