4.7 Article

Helical magnetic structure and hyperfine interactions in FeP studied by 57Fe Mossbauer spectroscopy and 31P NMR

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 675, Issue -, Pages 277-285

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2016.03.123

Keywords

Iron phosphide; Mossbauer spectroscopy; Noncollinear magnetism; NMR

Funding

  1. Russian Science Foundation [14-13-00089]
  2. Russian Foundation for Basic Research [15-03-99628]
  3. German Research Society DFG (Augsburg) [TRR80]
  4. German Research Society DFG (Munich) [TRR80]
  5. Russian Science Foundation [14-13-00089] Funding Source: Russian Science Foundation

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We report results of Fe-57 Mossbauer and P-31 NMR studies of a phosphide FeP powder sample performed in a wide temperature range including the point (T-N approximate to 120 K) of magnetic phase transitions. The Fe-57 Mossbauer spectra at low temperatures T < T-N present a very complex Zeeman pattern with line broadenings and sizeable spectral asymmetry. It was shown that the change of the observed spectral shape is consistent with the transition into a space-modulated helicoidal magnetic structure. Analysis of the experimental spectra was carried out assuming an anisotropy of the magnetic hyperfine field H-hf at the Fe-57 nuclei when the Fe3+ magnetic moment rotates with respect to the principal axis of the electric field gradient (EFG) tensor. The obtained large temperature independent anharmonicity parameter m approximate to 0.96 of the helicoidal spin structure results from easy-axis anisotropy in the plane of the iron spin rotation. It was assumed that a very low maximal value of H-hf(11 K) approximate to 36 kOe and its high anisotropy Delta H-anis(11 K) approximate to 30 kOe can be attributed to the stabilization of iron cations in the low-spin state (S-Fe = 1/2). The 31P NMR measurements demonstrate an extremely broad linewidth reflecting the spatial distribution of the transferred internal magnetic fields of the Fe3+ ions onto P sites in the magnetically ordered state. (C) 2016 Elsevier B.V. All rights reserved.

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