We studied the effect of naturally formed homointerfaces on the magnetic and electric transport behavior of a heavily twinned, 40 nm thick, pseudomorphic epitaxial film of La0.7Sr0.3MnO3 deposited by molecular beam epitaxy on ferroelastic LaAlO3(001) substrate. As proved by high resolution X-ray diffraction analysis, the lamellar twin structure of the substrate is imprinted in La0.7Sr0.3MnO3. In spite of the pronounced thermomagnetic irreversibility in the DC low field magnetization, spin-glass-like character, possibly related to the structural complexity, was ruled out, on the base of AC susceptibility results. The magnetic characterization indicates anisotropic ferromagnetism, with a saturation magnetization M-S = 3.2 mu(B)/Mn, slightly reduced with respect to the fully polarized value of 3.7 mu(B)/Mn. The low field DC magnetization vs temperature is non bulklike, with a two step increase in the field cooled M-FC(T) branch and a two peak structure in the zero field cooled M-ZFC(T) one. Correspondingly, two peaks are present in the resistivity vs temperature rho(T) curve. With reference to the behavior of epitaxial manganites deposited on bicrystal substrates, results are discussed in terms of a two phase model, in which each couple of adjacent ferromagnetic twin cores, with bulklike T-C = 370 K, is separated by a twin boundary with lower Curie point T-C = 150 K, acting as barrier for spin polarized transport. The two phase scenario is compared with the alternative one based on a single ferromagnetic phase with the peculiar ferromagnetic domains structure inherent to twinned manganites films, reported to be split into interconnected and spatially separated regions with in-plane and out-of-plane magnetization, coinciding with twin cores and twin boundaries respectively. (C) 2016 Elsevier B.V. All rights reserved.

Effect of natural homointerfaces on the magnetic properties of pseudomorphic La0.7Sr0.3MnO3 thin film: Phase separation vs split domain structure

Maritato Luigi;Orgiani Pasquale;
2016

Abstract

We studied the effect of naturally formed homointerfaces on the magnetic and electric transport behavior of a heavily twinned, 40 nm thick, pseudomorphic epitaxial film of La0.7Sr0.3MnO3 deposited by molecular beam epitaxy on ferroelastic LaAlO3(001) substrate. As proved by high resolution X-ray diffraction analysis, the lamellar twin structure of the substrate is imprinted in La0.7Sr0.3MnO3. In spite of the pronounced thermomagnetic irreversibility in the DC low field magnetization, spin-glass-like character, possibly related to the structural complexity, was ruled out, on the base of AC susceptibility results. The magnetic characterization indicates anisotropic ferromagnetism, with a saturation magnetization M-S = 3.2 mu(B)/Mn, slightly reduced with respect to the fully polarized value of 3.7 mu(B)/Mn. The low field DC magnetization vs temperature is non bulklike, with a two step increase in the field cooled M-FC(T) branch and a two peak structure in the zero field cooled M-ZFC(T) one. Correspondingly, two peaks are present in the resistivity vs temperature rho(T) curve. With reference to the behavior of epitaxial manganites deposited on bicrystal substrates, results are discussed in terms of a two phase model, in which each couple of adjacent ferromagnetic twin cores, with bulklike T-C = 370 K, is separated by a twin boundary with lower Curie point T-C = 150 K, acting as barrier for spin polarized transport. The two phase scenario is compared with the alternative one based on a single ferromagnetic phase with the peculiar ferromagnetic domains structure inherent to twinned manganites films, reported to be split into interconnected and spatially separated regions with in-plane and out-of-plane magnetization, coinciding with twin cores and twin boundaries respectively. (C) 2016 Elsevier B.V. All rights reserved.
2016
Istituto Superconduttori, materiali innovativi e dispositivi - SPIN
thin films
manganite
oxide
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/331733
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