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Jesche, A.

Publications and source records attributed to Jesche, A..

Ferromagnetism versus slow paramagnetic relaxation in Fe-doped Li 3 N

We report on isothermal magnetization, Mössbauer spectroscopy, and magnetostriction as well as temperature-dependent alternating-current (ac) susceptibility, specific heat, and thermal expansion of single crystalline and polycrystalline Li 2 ( Li 1-x Fe x ) N with x = 0 and x ≈ 0.30 . Magnetic hysteresis emerges at temperatures below T ≈ 50 K with coercivity fields of up to μ 0 H = 11.6 T at T = 2 K and magnetic anisotropy energies of 310 K (27 meV). The ac susceptibility is strongly frequency-dependent (f = 10 – 10 000 Hz) and reveals an effective energy barrier for spin reversal of Δ E ≈ 1100 K (90 meV). The relaxation times follow Arrhenius behavior for T > 25 K . For T < 10 K , however, the relaxation times of τ ≈ 10 10 s are only weakly temperature-dependent, indicating the relevance of a quantum tunneling process instead of thermal excitations. The magnetic entropy amounts to more than 25 J mol -1 Fe K -1 , which significantly exceeds R ln 2 , the value expected for the entropy of a ground-state doublet. Thermal expansion and magnetostriction indicate a weak magnetoelastic coupling in accordance with slow relaxation of the magnetization. The classification of Li 2 ( Li 1-x Fe x ) N as ferromagnet is stressed and contrasted with highly anisotropic and slowly relaxing paramagnetic behavior.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

X-Ray diffraction on large single crystals using a powder diffractometer

Information on the lattice parameter of single crystals with known crystallographic structure allows for estimations of sample quality and composition. In many cases it is sufficient to determine one lattice parameter or the lattice spacing along a certain, high- symmetry direction, e.g. in order to determine the composition in a substitution series by taking advantage of Vegard’s rule. Here we present a guide to accurate measurements of single crystals with dimensions ranging from 200 μm up to several millimeter using a standard powder diffractometer in Bragg-Brentano geometry. The correction of the error introduced by the sample height and the optimization of the alignment are discussed in detail. Finally, in particular for single crystals with a plate-like habit, the described procedure allows for measurement of the lattice spacings normal to the plates with high accuracy on a timescale of minutes.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗