Crystal chemistry and electronic properties of the N = 2 Ruddlesden-Popper manganates: Unconventional CMR materials

Battle, P.D. and Blundell, S.J. and Cox, D.E. and Green, M.A. and Millburn, J.E. and Radaelli, P.G. and Rosseinsky, M.J. and Singleton, J. and Spring, L.E. and Vente, J.F. (1997) Crystal chemistry and electronic properties of the N = 2 Ruddlesden-Popper manganates: Unconventional CMR materials. In: Proceedings of the 1996 MRS Fall Symposium, Pittsburgh, PA, United States, Boston, MA, USA. (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided)

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Abstract

The crystallography and electronic properties of the Ln2-xSr1+xMn2O7 manganese oxides adopting the n = 2 Ruddlesden-Popper (RP) structure are discussed, focusing on the structural phase diagrams and electronic properties in the vicinity of the Mn +3.5 oxidation state and in particular the ease of synthesis of single phases of these materials.

Item Type: Conference or workshop item (Proceeding)
Additional information: Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Mater Res Soc Symp Proc [Field not mapped to EPrints] AD - Univ of Oxford, Oxford, United Kingdom [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints] A4 - MRS [Field not mapped to EPrints] C3 - Materials Research Society Symposium - Proceedings [Field not mapped to EPrints]
Uncontrolled keywords: Crystallography, Electronic properties, Magnetoresistance, Manganese, Oxidation, Oxides, Phase diagrams, Synthesis (chemical), Colossal magnetoresistance (CMR), Ruddlesden-Popper manganates, Ferromagnetic materials
Subjects: Q Science > QC Physics > QC173.45 Condensed Matter
Q Science > QD Chemistry > QD478 Solid State Chemistry
Divisions: Faculties > Sciences > School of Physical Sciences > Functional Materials Group
Depositing User: Giles Tarver
Date Deposited: 21 Oct 2015 14:10 UTC
Last Modified: 23 Oct 2015 11:57 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/51159 (The current URI for this page, for reference purposes)
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