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  • 1
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The novel compounds Nd3Fe29−xTx (T=V and Cr) have been successfully synthesized. Their x-ray patterns can be indexed with a monoclinic symmetry and the A2/m space group. The Curie temperatures of Nd3Fe29−xTx are 455 and 413 K for T=V and Cr, the saturation magnetization at 4.2 K and room temperature are 54.7 and 46.8 μB/f.u. for T=V and 49.9 and 32.2 μB/f.u. for T=Cr, and the anisotropy fields at 4.2 K and room temperature are 12.8 and 2.4 T for T=V and 9.1 and 1.2 T for T=Cr, respectively. The spin reorientations of the easy magnetization direction of Nd3Fe29−xTx are observed at around 230 K for T=V and 135 K for T=Cr, respectively. After nitrogenation the relative volume expansion was about 6%, Curie temperature of each nitride increased about 50%, and the transition temperature Tsr of the spin reorientations of the nitride also increased 145 K for T=V and 250 K for T=Cr, respectively, compared with its parent compound. Nitrogenation resulted in remarkable improvements in the saturation magnetization and anisotropy fields at 4.2 K and room temperature. Magnetohistory effects for Nd3Fe29−xTx and Nd3Fe29−xTxN4 (T=V and Cr) in a low field have been observed. © 1997 American Institute of Physics.
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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.
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  • 3
    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.
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 70 (1991), S. 4973-4975 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A theoretical and experimental investigation of coupling effects in triple quantum wells is presented. Photoluminescence spectra of various triple coupled well structures prepared by metalorganic chemical vapor deposition show the effects of the well width on the electron to heavy hole transition energy and on the full width of half maximum. Also, the experimental results are compared to the time-independent solutions of the Schrödinger equation obtained by the inverse power method.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 1529-1538 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Fe K-edge extended x-ray absorption fine structure (EXAFS) data are presented for ferric neutralized Nafion membranes treated in various ways. The transmission experiments were performed at room temperature. Some complementary Mössbauer data are also provided. Attention is focused on the second major peak in the EXAFS radial structure functions. In ferric neutralized Nafion, whether dehydrated in air or under reduced pressure, this peak is attributed to the neighboring Fe of an oxo-bridged dimer, Fe–O–Fe. This dimer transforms into a dihydroxo-bridged dimer Fe OHOH Fe upon heating to 150 °C in vacuo. If the heat treatment is done in water then microcrystalline Fe2O3 is formed. Immersion of the ferric neutralized Nafion membrane in KCl, K2CO3, KOH aqueous solutions, or even exposure to NH4OH vapor, results in precipitation of iron inside the membrane. The precipitate has a Fe–O distance of 1.94±0.02 A(ring) and a Fe–Fe distance of 3.11±0.05 A(ring). Edge-sharing FeO6 octahedra form the basis of the precipitate structure.
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  • 6
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 52 (1988), S. 138-140 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Thin layers of ZnO were grown on (0001) oriented sapphire by organometallic chemical vapor deposition. Low-temperature photoluminescence indicates that near-band-edge luminescence dominates the spectrum. In contrast to bulk grown material deep level luminescence for the layers is relatively weak.
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 83 (1998), S. 4366-4372 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A systematic investigation of crystallographic and magnetic properties of nitride R3Fe29−xCrxN4 (R=Y, Ce, Nd, Sm, Gd, Tb, and Dy) has been performed. The lattice constants and unit cell volume decrease with increasing rare earth atomic number from Nd to Dy, reflecting the lanthanide contraction. After nitrogenation the relative volume expansion of each nitride is around between 5% and 7%. The nitrogenation results in a good improvement in the Curie temperature, the saturation magnetization and anisotropy fields at 4.2 K, and room temperature for R3Fe29−xCrxN4. Magnetohistory effects of R3Fe29−xCrxN4 and R3Fe29−xCrx (R=Nd and Sm) are observed in a low field of 0.04 T. First order magnetization process occurs in Sm3Fe24.0Cr5.0N4 in magnetic fields of 2.8 T at 4.2 K. After nitrogenation, the easy magnetization direction of Sm3Fe24.0Cr5.0 is changed from the easy-cone structure to the uniaxial. The good intrinsic magnetic properties of Sm3Fe24.0Cr5.0N4 make this compound a hopeful candidate for new high-performance hard magnets. © 1998 American Institute of Physics.
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  • 8
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 33 (1994), S. 2996-3003 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 34 (1962), S. 1356-1356 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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