Magnetic ordering in the rare earth intermetallic compound Tb2Ti3Ge4: Magnetization and neutron diffraction studies

被引:0
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作者
Malik, S. K. [1 ]
Lamsal, Jagat [2 ]
de Almeida, R. L. [1 ]
Quezado, S. [1 ]
Yelon, W. B. [3 ,4 ]
Garlea, V. O. [5 ]
Morozkin, A. V. [6 ]
Nirmala, R. [7 ]
机构
[1] Univ Brasilia, ICCMP, BR-70904970 Brasilia, DF, Brazil
[2] Univ Missouri, Dept Phys & Astron, Columbia, MO 65211 USA
[3] Missouri Univ Sci & Technol, Dept Chem, Rolla, MO 65409 USA
[4] Missouri Univ Sci & Technol, Mat Res Ctr, Rolla, MO 65409 USA
[5] Oak Ridge Natl Lab, Neutron Scattering Sci Div, Oak Ridge, TN 37831 USA
[6] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119899, Russia
[7] Indian Inst Technol, Dept Phys, Madras 600036, Tamil Nadu, India
关键词
ER;
D O I
10.1063/1.3063073
中图分类号
O59 [应用物理学];
学科分类号
摘要
Magnetization and neutron diffraction studies on a polycrystalline Tb2Ti3Ge4 sample (orthorhombic Sm5Ge4-type structure, space group Pnma, No. 62) have been carried out. This compound is found to order antiferromagnetically at similar to 18 K (T-N). The magnetization (M) versus field (H) isotherms obtained at 2, 3, 5, and 10 K indicate a field-induced antiferromagnetic to ferromagnetic transition in fields of the order of 0.5 T. The saturation magnetization value at 2.5 K (M extrapolated to 1/H -> 0) is only similar to 5.6 mu(B)/Tb3+, suggesting the possible presence of crystal field effects with or without a persisting antiferromagnetic component. Neutron powder diffraction data at 10 K confirm the existence of a magnetic long range order. Modeling of the magnetic scattering reveals a complex and incommensurate antiferromagnetic spin structure below T-N. (C) 2009 American Institute of Physics. [DOI: 10.1063/1.3063073]
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页数:3
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