Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/202317
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Título

Nanoscale magnetic and charge anisotropies at manganite interfaces

AutorCarreira, Santiago J.; Aguirre, Myriam H. CSIC ORCID; Briatico, Javier; Steren, Laura B.
Fecha de publicación2019
EditorRoyal Society of Chemistry (UK)
CitaciónRSC Advances 9(66): 38604-38611 (2019)
ResumenStrong correlated manganites are still under intense research owing to their complex phase diagrams in terms of Sr-doping and their sensitivity to intrinsic and extrinsic structural deformations. Here, we performed X-ray absorption spectroscopy measurements of manganite bilayers to explore the effects that a local Sr-doping gradient produce on the charge and antiferromagnetic anisotropies. In order to gradually tune the Sr-doping level along the axis perpendicular to the samples we have grown a series of bilayers with different thicknesses of low-doped manganites (from 0 nm to 6 nm) deposited over a La0.7Sr0.3MnO3 metallic layer. This strategy permitted us to resolve with high accuracy the thickness region where the charge and spin anisotropies vary and the critical thickness tc over which the out of plane orbital asymmetry does not have any further modifications. We found that the antiferromagnetic spin axis points preferentially out of the sample plane regardless the capping layer thickness. However, it tilts partially into the sample plane far from this critical thickness, owing to the combined contributions of the external structural strain and electron doping. Furthermore, we found that the doping level of the capping layer strongly affects the critical thickness, giving clear evidence of the influence exerted by the electron doping on the orbital and magnetic configurations. These anisotropic changes induce subtle modifications on the domain reorientation of La0.7Sr0.3MnO3, as evidenced from the magnetic hysteresis cycles.
Versión del editorhttps://doi.org/10.1039/C9RA06552K
URIhttp://hdl.handle.net/10261/202317
DOI10.1039/C9RA06552K
E-ISSN2046-2069
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