We study the multiferroic properties in the distorted tetrahedral quasi-one dimensional spin system Cu$_3$Mo$_2$O$_9$, in which the effects of the low dimensionality and the magnetic frustration are expected to appear simultaneously. We clarify that the antiferromagnetic order is formed together with ferroelectric properties at $T_{rm N}=7.9$ K under zero magnetic field and obtain the magnetic-field-temperature phase diagram by measuring dielectric constant and spontaneous electric polarization. It is found that the antiferromagnetic phase possesses a spontaneous electric polarization parallel to the c axis when the magnetic field $H$ is applied parallel to the a axis. On the other hand, there are three different ferroelectric phases in the antiferromagnetic phase for $H$ parallel to the c axis.
The magnetic and dielectric properties under high magnetic fields are studied in the single crystal of Cu3Mo2O9. This multiferroic compound has distorted tetrahedral spin chains. The effects of the quasi-one dimensionality and the geometrical spin frustration are expected to appear simultaneously. We measure the magnetoelectric current and the differential magnetization under the pulsed magnetic field up to 74 T. We also measure the electric polarization versus the electric field curve/loop under the static field up to 23 T. Dielectric properties change at the magnetic fields where the magnetization jumps are observed in the magnetization curve. Moreover, the magnetization plateaus are found at high magnetic fields.
Static magnetic susceptibility chi, ac susceptibility chi_{ac} and specific heat C versus temperature T measurements on polycrystalline samples of In2VO5 and chi and C versus T measurements on the isostructural, nonmagnetic compound In2TiO5 are reported. A Curie-Wiess fit to the chi(T) data above 175 K for In2VO5 indicates ferromagnetic exchange between V^{4+} (S = 1/2) moments. Below 150 K the chi(T) data deviate from the Curie-Weiss behavior but there is no signature of any long range magnetic order down to 1.8 K. There is a cusp at 2.8 K in the zero field cooled (ZFC) chi(T) data measured in a magnetic field of 100 Oe and the ZFC and field cooled (FC) data show a bifurcation below this temperature. The frequency dependence of the chi_{ac}(T) data indicate that below 3 K the system is in a spin-glass state. The difference Delta C between the heat capacity of In2VO5 and In2TiO5 shows a broad anomaly peaked at 130 K. The entropy upto 300 K is more than what is expected for S = 1/2 moments. The anomaly in Delta C and the extra entropy suggests that there may be a structural change below 130 K in In2VO5.
We report the results of ac and dc magnetization (M) and heat-capacity (C) measurements on the solid solution, Sr$_3$Cu$_{1-x}$Zn$_x$IrO$_6$. While the Zn end member is known to form in a rhombohedral pseudo one-dimensional K$_4$CdCl$_6$ structure with an antiferromagnetic ordering temperature of (T$_N$ =) 19 K, the Cu end member has been reported to form in a monoclinically distorted form with a Curie temperature of (T$_C$ =) 19 K. The magnetism of the Zn compound is found to be robust to synthetic conditions and is broadly consistent with the behavior known in the literature. However, we find a lower magnetic ordering temperature (T$_o$) for our Cu compound (~ 13 K), thereby suggesting that T$_o$ is sensitive to synthetic conditions. The Cu sample appears to be in a spin-glass-like state at low temperatures, judged by a frequency dependence of ac magnetic susceptibility and a broadening of the C anomaly at the onset of magnetic ordering, in sharp contrast to earlier proposals. Small applications of magnetic field, however, drive this system to ferromagnetism as inferred from the M data. Small substitutions for Cu/Zn (x = 0.75 or 0.25) significantly depress magnetic ordering; in other words, T$_o$ varies non-monotonically with x (T$_o$ ~ 6, 3 and 4 K for x = 0.25, 0.5, and 0.67 respectively). The plot of inverse susceptibility versus temperature is non-linear in the paramagnetic state as if correlations within (or among) the magnetic chains continuously vary with temperature. The results establish
We report magnetic susceptibility, specific heat, and Raman scattering investigations of alpha-TeVO4 containing V-O edge-sharing chains. These chains promote a system of ferromagnetic/antiferromagnetic spin-1/2 Heisenberg alternating exchange chains with pronounced spin frustration. The magnetic susceptibility and Raman scattering evidence a crossover at T* = 85 K with different slopes of the reciprocal susceptibility and a magnetic phase transition into a long-range-ordered state at Tc = 16 K. From Raman scattering data a strong mutual coupling between lattice and magnetic degrees of freedom is deduced. A comparison to model calculations and prior Raman scattering on other chain systems yield a plausible interpretation of the microscopic mechanism for the crossover behavior.
We report an investigation on structure and magnetic properties of the $S=3/2$ zigzag spin chain compound BaCoTe$_2$O$_7$. Neutron diffraction measurements reveal BaCoTe$_2$O$_7$ crystallizes in the noncentrosymmetric space group $Ama2$ with a canted $uparrowuparrowdownarrowdownarrow$ spin structure along the quasi-one-dimensional zigzag chain and a moment size of $1.89(2)mu_B$ at 2 K. Magnetic susceptibility and specific heat measurements yield an antiferromagnetic phase transition at $T_N=6.2$ K. A negative Curie-Weiss temperature $Theta_{CW}=-74.7(2)$ K and an empirical frustration parameter of $f=|Theta_text{CW}|/T_text{N}approx12$ is obtained from fitting the magnetic susceptibility, indicating antiferromagnetic interactions and strong magnetic frustration. By employing ultraviolet-visible absorption spectroscopy and first principles calculations, an indirect band gap of 2.68(2) eV is determined. We propose that the canted zigzag spin chain of BaCoTe$_2$O$_7$ may produce a change of the polarization via exchange striction mechanism.
T. Hosaka
,S. Hachiuma
,H. Kuroe
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(2011)
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"Magnetic and electric properties in the distorted tetrahedral spin chain system Cu3Mo2O9"
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Haruhiko Kuroe
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