Pressure effects on magnetic and structural properties of pure and substituted SrRuO3

被引:9
|
作者
Pietosa, J. [1 ]
Dabrowski, B. [2 ,3 ]
Wisniewski, A. [1 ]
Puzniak, R. [1 ]
Kiyanagi, R. [4 ]
Maxwell, T. [2 ]
Jorgensen, J. D. [3 ]
机构
[1] Polish Acad Sci, Inst Phys, PL-02668 Warsaw, Poland
[2] No Illinois Univ, Dept Phys, De Kalb, IL 60115 USA
[3] Argonne Natl Lab, Div Mat Sci, Argonne, IL 60439 USA
[4] Argonne Natl Lab, Div Intense Pulsed Neutron Source, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
D O I
10.1103/PhysRevB.77.104410
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
An influence of hydrostatic pressure on phase transition temperature T-C, spontaneous magnetization M-0, coercive field H-C, and remanent magnetization M-R, has been investigated for the parent perovskite SrRuO3 and substituted ruthenates with decreased (La0.2Sr0.8RuO3, SrRu0.9Mn0.1O3) and increased (SrRu0.9Cr0.1O3) Curie temperature. We have observed a decrease of TC with pressure for all of the studied samples, however, the lowering of T-C with pressure (dT(C)/ dP) is not correlated with the value of T-C at ambient pressure. The spontaneous magnetization and coercive field remain unchanged for most of the samples, except the La0.2Sr0.8RuO3 sample, where spontaneous magnetization decreases with increasing pressure. For SrRuO3, structural study by neutron powder diffraction shows clear contraction of the Ru-O bond lengths under external pressure whereas bond angles and the orthorhombic distortion remain constant at 295 and 50 K. The weakening of the ferromagnetic interactions with increasing pressure is consistent with complex band structure effects through a combination of modulation of the hybridization caused by contraction of the Ru-O bonds and with the significant role of the direct Ru-Ru interactions.
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页数:6
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