Abstract

Metal-insulator transition is observed in the La0.8Sr0.2MnO3 thin films with thickness larger than 5 unit cells. Insulating phase at lower temperature appeared in the ultrathin films with thickness ranging from 6 unit cells to 10 unit cells and it is found that the Mott variable range hopping conduction dominates in this insulating phase at low temperature with a decrease of localization length in thinner films. A deficiency of oxygen content and a resulting decrease of the Mn valence have been observed in the ultrathin films with thickness smaller than or equal to 10 unit cells by studying the aberration-corrected scanning transmission electron microscopy and electron energy loss spectroscopy of the films. These results suggest that the existence of the oxygen vacancies in thinner films suppresses the double-exchange mechanism and contributes to the enhancement of disorder, leading to a decrease of the Curie temperature and the low temperature insulating phase in the ultrathin films. In addition, the suppression of the magnetic properties in thinner films indicates stronger disorder of magnetic moments, which is considered to be the reason for this decrease of the localization length.

Highlights

  • MethodsLSMO films were deposited on (001) cut TiO2-terminated STO substrates by a computer-controlled laser molecular beam epitaxy (Laser-MBE) equipped with an in situ reflection high-energy electron diffraction (RHEED) system (PASCAL) allowing for precise control of the thickness at the atomic scale

  • The surface topography of the films is further characterized by the atomic force microscopy (AFM) and an atomically flat step-and-terrace surface can be seen in the AFM image of the 10 u.c. film (Fig. 1b)

  • The crystal structure of the LSMO thin films is characterized by the high-resolution transmission electronic microscopy (TEM), and the high-angle annular dark-field (HAADF) micrograph of the 10 u.c

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Summary

Methods

LSMO films were deposited on (001) cut TiO2-terminated STO substrates by a computer-controlled laser molecular beam epitaxy (Laser-MBE) equipped with an in situ reflection high-energy electron diffraction (RHEED) system (PASCAL) allowing for precise control of the thickness at the atomic scale. A XeCl 308 nm excimer laser was used with an energy density of 2.18 J/cm[2] and a repetition rate of 2 Hz. The films were deposited at 930 °C with the oxygen pressure of 30 Pa. After deposition, the samples were in-situ annealed for 10 min, and cooled down to room temperature. The surface morphology of the LSMO films was recorded using a commercial atomic force microscopy (AFM) system (Asylum Research MFP3D)

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