Changes in the electronic structure and spin dynamics across the metal-insulator transition in La1-xSrxCoO3

被引:2
|
作者
Smith, R. X. [1 ,3 ]
Hoch, M. J. R. [1 ]
Moulton, W. G. [1 ]
Kuhns, P. L. [1 ]
Reyes, A. P. [1 ]
Boebinger, G. S. [1 ]
Zheng, H. [2 ]
Mitchell, J. F. [2 ]
机构
[1] Florida State Univ, Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[2] Argonne Natl Lab, Div Mat Sci, 9700 S Cass Ave, Argonne, IL 60439 USA
[3] Univ Calif Los Angeles, Dept Neurol, Lab FMRI Technol LOFT, Ahmanson Lovelace Brain Mapping Ctr, Los Angeles, CA 90024 USA
基金
美国国家科学基金会;
关键词
NUCLEAR MAGNETIC RELAXATION;
D O I
10.1103/PhysRevB.93.024204
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The magnetoelectronic properties of La1-xSrxCoO3, which include giant magnetoresistance, are strongly dependent on the level of hole doping. The system evolves, with increasing x, from a spin glass insulator to a metallic ferromagnet with a metal-insulator (MI) transition at x(C) similar to 0.18. Nanoscale phase separation occurs in the insulating phase and persists, to some extent, into the just-metallic phase. The present experiments at 4.2 K have used La-139 nuclear magnetic resonance to investigate the transition from hopping dynamics for x < x(C) to Korringa-like ferromagnetic metal behavior for x > x(C). A marked decrease in the spin-lattice relaxation rate is found in the vicinity of x(C) as the MI transition is crossed. This behavior is accounted for in terms of the evolution of the electronic structure and dynamics with cluster size.
引用
收藏
页数:6
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