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  • 1995-1999  (7)
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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 79 (1996), S. 7883-7886 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A study on the exchange interaction in R2Fe17 compounds (R represents the heavy rare earth elements) has been performed by means of a mean-field analysis of the high-field magnetization curves, which were measured on the powder samples. Measurements have been carried out on R2Fe17-based quasiternary R2Fe17−xMx compounds with R=Dy, Ho, and Er, M=Al, Ga, and Si. It has been found that the value of the exchange coupling constant decreases with increasing atomic number of R ion of the compound. This behavior is explained by the varying 4f–5d hybridization in the compounds. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 81 (1997), S. 7450-7457 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A systematic investigation of structure and intrinsic magnetic properties of the novel compounds R3(Fe, T)29 (R=Y, Ce, Nd, Sm, Gd, Tb, and Dy; T=V and Cr) has been performed. The lattice constants and unit cell volume decrease with increasing the rare-earth atomic number from R=Nd to Dy, except for Ce, reflecting the lanthanide contraction. The Curie temperature increases from R=Ce to Gd and decreases from Gd to Dy, respectively, with increasing atomic number and Gd3Fe29−xTx has the highest Curie temperature for each series of R3Fe29−xTx (T=V or Cr) compounds. The saturation magnetization of R3Fe29−xTx at 4.2 K decreases gradually from R=Nd to Dy with increasing atomic number, except for Ce, in each series of R3Fe29−xTx. It is suggested that the Ce ion in Ce3Fe29−xTx is valence fluctuated which leads to the unusual magnetic properties. The spin reorientations of the easy magnetization direction of R3Fe29−xTx are observed at around 230, 230, and 160 K for R=Nd, Sm, and Tb when T=V, and at around 230 and 180 K for R=Nd and Tb when T=Cr, respectively. First order magnetization processes are observed around 5.7 T for Sm3Fe26.7V2.3 and 4 T for Sm3Fe24.0Cr5.0 at 4.2 K, 2.0 T for Tb3Fe28.0V1.0, and 2.3 T for Tb3Fe28.0Cr1.0 at room temperature. A phenomenological analysis shows that the saturation magnetization of R3Fe29−xTx compounds with a low T concentration can be roughly calculated based on a combination of those of the 2:17R and 1:12 units in a ratio of 1:1. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 79 (1996), S. 6321-6323 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The temperature dependence of the magnetization of DyCo10−xNixSi2 compounds with x=0, 2, 4, and 6 was measured in fields up to 5.0 T and in the temperature range from 4.2 to 300 K in a SQUID magnetometer. Compensation temperatures were observed for the compounds with x=4 and 6. The values of the R-T exchange interaction obtained by fitting the M-T curves on the basis of two-sublattice molecular-field theory are compared with the values obtained from high-field magnetization measurements on powder particles free to be oriented by the applied field. In all four compounds magnetic transitions are found in the ac-susceptibility measurements which were carried out between 4.2 K and room temperature. The types of magnetic anisotropy were investigated by magnetization measurements on samples that were magnetically aligned at room temperature. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 85 (1999), S. 4684-4686 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Structural and magnetic properties of RFe11.3Nb0.7 compounds with rare-earth elements (R=Y, Sm, Gd, Tb, Dy, Ho, and Er) have been investigated. The Curie temperature increases for R=Sm–Gd, then decreases from R=Gd to Er. In the compound with R=Tb, with increasing temperature, a spin reorientation from an easy magnetization direction in the plane to an easy cone occurs at 365 K. In the compound with R=Er, a spin reorientation from easy plane to easy axis is found at about 40 K. Two spin reorientations take place in the compound with R=Dy, from easy plane to a complex structure at 125 K and from complex structure to easy axis at 210 K. At room temperature, the easy magnetization direction is along the c axis for R=Y, Sm, Gd, Dy, Ho, and Er, and in the plane for R=Tb. Studies of the magnetic anisotropy in YFe11.3Nb0.7 and GdFe11.3Nb0.7 point out that the Fe sublattice anisotropy is of easy axis type. In HoFe11.3Nb0.7, a first-order magnetization process takes place below 150 K when an external magnetic field is applied along the hard magnetization direction. The exchange-interaction constants JR–Fe decreases with increasing atomic number of R, as is generally found in rare-earth transition-metal compounds. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 80 (1996), S. 6898-6902 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The structure and magnetic properties of SmMn2(Ge1−xSix)2 compounds (x=0–1.0) have been investigated. All the compounds crystallize in ThCr2Si2-type structure. Substitution of Si for Ge leads to a linear decrease of the lattice constants and the unit-cell volume. In all compounds a transition from the ferromagnetic to the antiferromagnetic state is observed at a lower temperature T1, which first decreases, goes through a minimum at x=0.4–0.6, and then increases again with Si concentration. As temperature increases, for the compounds with x〈0.3 both a antiferromagnetic–ferromagnetic transition and the ferromagnetic–paramagnetic transitions are observed as well at T2 and at the Curie temperature Tc, respectively. With increasing Si content the Tc decreases, whereas T2 increases from 140 K for x=0 to 215 K for x=0.2. For compounds with x≥0.3 the antiferromagnetic–paramagnetic transition was observed with increasing temperature and the Néel temperature increases with increasing Si content. The saturation magnetization at 1.5 K decreases first, goes through a minimum at x=0.6, and then increases again with increasing Si content. At room temperature, the saturation magnetization decreases monotonically from 3.27 μB/f.u. for x=0 to nearly zero for x=0.3. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 81 (1997), S. 3248-3252 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A systematic investigation of the structure and magnetic properties of novel compounds Tb3(Fe1−xVx)29 (x=0.033, 0.044, 0.056, and 0.061) has been performed. The lattice parameters and Curie temperatures are obtained. The saturation magnetization of Tb3(Fe1−xVx)29 decreases but the anisotropy field increases linearly with increasing V concentration at 4.2 K and room temperature. The spin reorientations of the easy magnetization direction of Tb3(Fe1−xVx)29 occur at around 160 K. A first order magnetization process of Tb3(Fe1−xVx)29 is observed with magnetic field in the range between 2.0 and 1.6 T at room temperature. The saturation magnetization of Tb3Fe29−yVy with a low V concentration at 4.2 K can be roughly calculated based on a combination of that of the Tb2Fe17 and TbFe12−yVy units in a ratio of 1:1. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-2665
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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