
Localized to Itinerant Electronic Transition in Perovskite Oxides
Goodenough, John B. (EDT)/ Cooper, S. L./ Egami, T./ Zhou, J. S./ Bard, A./ Dance, I. G./ Day, P. (EDT)/ Ibers, J. A. (EDT)/ Kunitake, T. (EDT)/ Meyer, Thomas J. (EDT)/ Mingos, D. M. P. (EDT)/ Roesky, H. W. (EDT)/ Sauvage, J. P. (EDT)/ Simon, A. (EDT)
Takealot · checked 7 days ago
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- R 9 630.50
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- R 9 088.00
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- R 250.00
- First indexed
- 22 Sep 2026
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Description
Interest in the transition metal oxides with perovskite related structures goes back to the 1950s when the sodium tungsten bronzes NaxWO3 were shown to be metallic 1 ], the system Lal_xSr MnO3 was found to contain a ferromagnetic conductive phase 2], and La0.sSr0.sCoO3 was reported to be a ferromagnetic metal, but with a peculiar magnetization of 1.5 #a/Co atom 3]. Stoichiometric oxide perovskites have the generic formula AMO3 in which the A site is at the center of a simple cubic array of M sites; the oxide ions form (180 4)) M O M bridges to give an MO3 array of corner shared MO6/2 octahedra and the larger A cations have twelvefold oxygen coordination. Mismatch between the A O and M O equilibrium bond lengths introduces internal stresses. A compressive stress on the MO3 array is accommodated by a lowering of the M O M bond angle from 180 to (180 4)); a tensile stress on the M O M bonds is accommodated by the formation of hexagonal polytypes 4].