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Magnetic field dependent cycloidal rotation in pristine and Ge doped CoCr$_2$O$_4$

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 Publication date 2020
  fields Physics
and research's language is English




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We report a soft x-ray resonant magnetic scattering study of the spin configuration in multiferroic thin films of Co$_{0.975}$Ge$_{0.025}$Cr$_2$O$_4$ (Ge-CCO) and CoCr$_2$O$_4$ (CCO), under low- and high-magnetic fields, from 0.2 T up to 6.5 T. A characterization of Ge-CCO at a low magnetic field is performed and the results are compared to those of pure CCO. The ferrimagnetic phase transition temperature $T_C approx 95$ K and the multiferroic transition temperature $T_S approx 27$ K in Ge-CCO are comparable to those observed in CCO. In Ge-CCO, the ordering wave vector $textit{(qq0)}$ observed below $T_S$ is slightly larger compared to that of CCO, and, unlike CCO, the diffraction intensity consists of two contributions that show a dissimilar x-ray polarization dependence. In Ge-CCO, the coercive field observed at low temperatures was larger than the one reported for CCO. In both compounds, an unexpected reversal of the spiral helicity and therefore the electric polarization was observed on simply magnetic field cooling. In addition, we find a change in the helicity as a function of momentum transfer in the magnetic diffraction peak of Ge-CCO, indicative of the presence of multiple magnetic spirals.



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We study $S=1/2$ dimer excitation in a coupled chain and dimer compound Cu$_2$Fe$_2$Ge$_4$O$_{13} by inelastic neutron scattering technique. The Zeeman split of the dimer triplet by a staggered field is observed at low temperature. With the increase of temperature the effect of random field is detected by a drastic broadening of the triplet excitation. Basic dynamics of dimer in the staggered and random fields are experimentally identified in Cu$_2$Fe$_2$Ge$_4$O$_{13}.
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