Theory of Ionic Ordering, Crystal Distortion, and Magnetic Exchange Due to Covalent Forces in Spinels

J. B. Goodenough and A. L. Loeb
Phys. Rev. 98, 391 – Published 15 April 1955
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Abstract

Elastic- and electrostatic-energy considerations are insufficient for an explanation of cation ordering between tetrahedral and octahedral sites in spinels. Tetrahedral, octahedral, and square covalent bonds are also important when cations are to be accommodated in these sites. The square bonds in octahedral sites can cause the tetragonal distortion observed in Mn3O4 γ-Mn2O3, ZnMn2O4, CuFe2O4, CuCr2O4, CaIn2O4, CdIn2O4, and metallic indium. A new magnetic exchange mechanism, "semicovalent exchange," which is consistent with the covalent model, is used to explain the magnetic properties of spinels.

  • Received 1 September 1954

DOI:https://doi.org/10.1103/PhysRev.98.391

©1955 American Physical Society

Authors & Affiliations

J. B. Goodenough and A. L. Loeb

  • Lincoln Laboratory, Massachusetts Institute of Technology, Lexington, Massachusetts

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Issue

Vol. 98, Iss. 2 — April 1955

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