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تسجيل مستخدم جديدMagnetic behavior of nano crystals of a spin-chain system, Ca3Co2O6: Absence of multiple steps in the low temperature isothermal magnetization
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We report that the major features in the temperature dependence of dc and ac magnetization of a well-known spin-chain compound, Ca3Co2O6, which has been known to exhibit two complex magnetic transitions due to geometrical frustration (one near 24 K and the other near 10 K), are found to be qualitatively unaffected in its nano form synthesized by high-energy ball-milling. However, the multiple steps in isothermal magnetization - a topic of current interest in low-dimensional systems - known for the bulk form well below 10 K is absent in the nano particles. We believe that this finding will be useful to the understanding of the step magnetization behavior of such spin-chain systems.
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The magnetic behavior of the Ca3Co2O6 spin chain compound is characterized by a large Ising-like character of its ferromagnetic chains, set on triangular lattice, that are antiferromagnetically coupled. At low temperature, T < 7K, the 3D antiferromag
netic state evolves towards a spin frozen state. In this temperature range, magnetic field driven magnetization of single crystals (H//chains) exhibits stepped variations. The occurrence of these steps at regular intervals of the applied magnetic field, Hstep=1.2T, is reminiscent of the quantum tunneling of the magnetization (QTM) of molecular based magnets. Magnetization relaxation experiments also strongly support the occurrence of this quantum phenomenon. This first observation of QTM in a magnetic oxide belonging to the large family of the A3BBO6 compounds opens new opportunities to study a quantum effect in a very different class of materials from molecular magnets.
Using powder neutron diffraction we have discovered an unusual magnetic order-order transition in the Ising spin chain compound Ca3Co2O6. On lowering the temperature an antiferromagnetic phase with propagation vector k=(0.5,-0.5,1) emerges from a hig
her temperature spin density wave structure with k=(0, 0, 1.01). This transition occurs over an unprecedented time-scale of several hours and is never complete.
Using inelastic neutron scattering, we have observed a quasi-one-dimensional dispersive magnetic excitation in the frustrated triangular-lattice spin-2 chain oxide Ca3Co2O6. At the lowest temperature (T = 1.5 K), this magnon is characterized by a lar
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We have recently reported that the Haldane spin-chain system, Er2BaNiO5, undergoing antiferromagnetic order below 32 K, is characterized by the onset of ferroelectricity near 60K due to magnetoelectric coupling induced by short-range magnetic-order w
ithin spin-chains. We have carried out additional magnetic and dielectric studies to understand the properties well below antiferromagnetic ordering temperature. We emphasize here on the following: (i) A strong frequency dependent behaviors of ac magnetic susceptibility and complex dielectric properties have been observed at much lower temperatures (below 8 K), that is, reentrant multiglass-like phenomenon, naturally suggesting the existence of an additional transition well below Neel temperature; ii) Magnetoelectric phase coexistence is observed at very low temperature (e.g., T =2K), where the high-field magnetoelectric phase is partially arrested on returning to zero magnetic field after a cycling through metamagnetic transition.
We study the low-temperature heat transport, as well as the magnetization and the specific heat, of TmMnO_3 single crystals to probe the transitions of magnetic structure induced by magnetic field. It is found that the low-T thermal conductivity (kap
pa) shows strong magnetic-field dependence and the overall behaviors can be understood in the scenario of magnetic scattering on phonons. In addition, a strong dip-like feature shows up in kappa(H) isotherms at 3.5--4 T for H parallel c, which is related to a known spin re-orientation of Mn^{3+} moments. The absence of this phenomenon for H parallel a indicates that the magnetic-structure transition of TmMnO_3 cannot be driven by the in-plane field. In comparison, the magnetothermal conductivity of TmMnO_3 is much larger than that of YMnO_3 but smaller than that of HoMnO_3, indicating that the magnetisms of rare-earth ions are playing the key role in the spin-phonon coupling of the hexagonal manganites.
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