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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Physics and chemistry of minerals 22 (1995), S. 259-267 
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract Mössbauer measurements on synthetic iron orthosilicate Fe2SiO4 (fayalite) were carried out in the antiferromagnetic spin state below T N ≃65 K. The Mössbauer parameters isomer shift δ, inner magnetic field H(0), angle Θ between H(0) and the z-component of the electric field gradient (efg), quadrupole splitting QS and asymmetry parameter η were determined as a function of temperature. These parameters could be attributed to the two crystallographic sites M1 and M2. The smaller isomer shift on M1 with respect to M2 displays the more covalent character of the Fe-O bond on M1, which is supported by previous neutron diffraction experiments. H(0) shows a Brillouin-type behaviour with different fields on the two crystallographic sites (stronger on M1) and a small discontinuity at T = 23 K which corresponds with previous magnetic measurements. The quadrupole splitting is equal on both sites within error bars, in agreement with previous theoretical results and in contradiction to previous Mössbauer refinements published elsewhere. Single crystal Mössbauer spectroscopy revealed the orientation of the crystallographic c-axis (Pnma) with respect to the axes of the efg. A second parameter set which also holds true for the powder refinement yields the angle between c and H(0) on M1 to be temperature-dependent in quantitative agreement with previous neutron diffraction results and solves an old discrepancy discussed elsewhere. On M2, the angle between c and H(0) is found to be much smaller than 90° in contradiction to symmetry requirements.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2021
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Abstract The present work reports Mössbauer investigations for several temperatures below T N on fayalite single crystal sections cut perpendicularly to the crystallographic a and b-axis (Pnma). The previously detected correspondence between the c-component of the magnetic moment on M1 from neutron diffraction and our own Mössbauer measurements published elsewhere are confirmed for the other principal sections to a large extent. Small humps in the angular dependence of two components of the internal magnetic field H(0) on T below T=23 K are in good agreement with magnetometric and calorimetric data published elsewhere; a reinterpretation of single reflection neutron data has been possible by our results. Moreover, the axes of the electric field gradient (efg) are oriented within the crystallographic axes for the M1-site at low temperatures. The violation of symmetry on the M2 position as a result of our previous investigations could be confirmed for the section ⊥ a, but not with respect to b. A possible explanation in terms of saturation effects of large line intensities at the expense of the small ones is given in the context.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Mineralogy and petrology 43 (1990), S. 73-81 
    ISSN: 1438-1168
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Description / Table of Contents: Zusammenfassung Die Rolle von Fe2+ und Fe3+ in synthetischen Tetraedriten mit Fe-Substitution Tetraedrite mit einer Zusammensetzung zwischen Cu12Sb4S13 and Cu10Fe2Sb4S13 wurden bei 457 °C und 500 °C aus den Elementen synthetisiert und sorgfdltig mit Mössbauer-Spektroskopie von57Fe untersucht. Zwischen Cu12Sb4S13 and Cu11Fe1Sb4S13 ist Eisen überwiegend dreiwertig. Zwischen Cu11Fe1Sb4S13 and Cu11Fe2Sb4S13 ist Eisen überwiegend zweiwertig und besetzt die tetraedrisch koordinierten M1-Plätze.
    Notes: Summary Tetrahedrites with the composition between Cu12Sb4S13 and Cu10Fe2Sb4S13 were synthesized at 457 °C and 500 °C from the elements and carefully studied by Mössbauer spectroscopy of57Fe. Between Cu12Sb4S13 and Cu11Fe1Sb4S13 iron is predominantly ferric. Between Cu11Fe1Sb4S13 and Cu10Fe2Sb4S13 iron is predominantly ferrous and occupies the tetrahedral M1-sites.
    Type of Medium: Electronic Resource
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