Structural, magneto transport and magnetic properties of Ruddlesden–Popper La2-2xSr1+2xMn2O7 (0.42≤x≤0.52) layered manganites
Author(s) -
Ajay Kumar Saw,
Shalabh Gupta,
Vijaylakshmi Dayal
Publication year - 2021
Publication title -
aip advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.421
H-Index - 58
ISSN - 2158-3226
DOI - 10.1063/9.0000109
Subject(s) - condensed matter physics , magnetoresistance , electrical resistivity and conductivity , variable range hopping , antiferromagnetism , magnetization , materials science , ferromagnetism , charge ordering , rietveld refinement , tetragonal crystal system , colossal magnetoresistance , chemistry , magnetic field , crystal structure , charge (physics) , physics , crystallography , quantum mechanics
The magneto transport of Ruddlesden–Popper, La2-2xSr1+2xMn2O7 (0.42≤x≤0.52), 2-dimensional bilayered manganites have been investigated in a broad temperature range. The samples have been synthesized using the solid-state reaction method. Rietveld refinement of the X-ray diffraction data indicates the tetragonal structure formation with I4/mmm space group. The resistivity curves of the samples present a general characteristic of metal-insulator (MI) transition at certain temperature (TMI). Besides, for samples with x = 0.48, 0.50, and 0.52, at a certain temperature (TCO) well below TMI the charge ordering is also evident. Furthermore, the samples display a shallow upturn in resistivity below Tmin due to the Kondo like spin scattering effect, weak localization and electron-phonon interaction. The high temperature semiconducting (T>TMI) region, the resistivity curve follows the 3D Mott’s variable hopping transport mechanism. The overall suppression of resistivity accounts for a substantial magnetoresistance by applying a magnetic field and the characteristic change in TMI, TCO, and Tmin are discussed. Temperature-dependent magnetization demonstrates the suppression of ferromagnetism and evident of antiferromagnetic nature with an apparent charge ordering with increasing concentration of Sr2+.
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