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Title

On the origin of the magnetism of Mn-Zn-O systems: Structural, electronic, and magnetic study of exotic MnO 2-δ/ZnO thin films

AuthorsCéspedes, Eva ; Laguna-Marco, M. A.; Jiménez-Villacorta, Félix ; Chaboy, Jesús; Boada, R.; Guglieri, C.; Andrés, Alicia de ; Prieto, C.
Issue Date2011
PublisherAmerican Chemical Society
CitationJournal of Physical Chemistry C 115(49): 24092-24101 (2011)
AbstractThe structural, electronic, and magnetic characterization of sputtered MnO 2-δ/ZnO films showing room temperature ferromagnetism has been carried out by a number of techniques. To elucidate the origin of the ferromagnetic order, a novel approach by studying XAS and XMCD signals at both Mn and Zn K edges in combination with the macroscopic magnetization measurements has been performed. The analysis of the XAS profile at the Mn edge indicates the coexistence of Mn 4+/Mn 3+ with a slightly distorted MnO 2-δ environment. The XMCD signal at the Zn K edge indicates the existence of an intrinsic magnetic moment in Zn. The Zn edge dichroic intensity is, however, 1 order of magnitude lower than in the case of Mn, being the magnetic moment of Mn, 2.1-2.4 μ B per Mn cation participating in the ferromagnetic phase, the main contribution to the total magnetization. The ferromagnetic phase has been assigned to high-density regions of Mn cations with a MnO 2-δ distorted environment, mainly allocated at the nonstoichiometric and highly defective ZnO grain boundaries, with a sufficient extension to overcome the thermal energy over room temperature. The ferromagnetic coupling has been related to modifications of the Mn-O-Mn bonds, distances, and angles, promoted by neighboring ZnO and forming stable magnetic configurations that lead to new forms of exchange interaction: ferromagnetic superexchange or a double-exchange mechanism between the Mn 4+ and Mn 3+. Highly defective regions and structural distortions, together with complex Mn oxidation states, appear to be key features in the magnetic properties of Mn-Zn-O. © 2011 American Chemical Society.
URIhttp://hdl.handle.net/10261/53595
DOI10.1021/jp208929w
Identifiersdoi: 10.1021/jp208929w
issn: 1932-7447
e-issn: 1932-7455
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