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Register a new userAntiferromagnetic Order in Disorder-Induced Insulating Phase of SrRu_{1-x}Mn_xO_3 (0.4<x<0.6)
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We have performed the powder neutron diffraction measurements on the solid solutions of SrRu_{1-x}Mn_xO_3, and found that the itinerant ferromagnetic order observed in pure SrRuO_3 changes into the C-type antiferromagnetic (AF) order with nearly localized d electrons in the intermediate Mn concentration between x=0.4 and 0.6. With increasing x, the AF moment is strongly enhanced from 1.1 mB (x=0.4) to 2.6 mB (x=0.6), which is accompanied by the elongation of the tetragonal c/a ratio. These results suggest that the substitution of Mn for Ru suppresses the itinerant character of the d electrons, and induces the superexchange interaction through the compression in the c plane. We have also found that the magnetic and transport properties observed in our tetragonal samples are quite similar to those of recently reported orthorhombic ones.
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Low-temperature electronic states in SrRu_{1-x}Mn_xO_3 for x <= 0.6 have been investigated by means of specific-heat C_p measurements. We have found that a jump anomaly observed in C_p at the ferromagnetic (FM) transition temperature for SrRuO_3 changes into a broad peak by only 5% substitution of Mn for Ru. With further doping Mn, the low-temperature electronic specific-heat coefficient gamma is markedly reduced from the value at x=0 (33 mJ/K^2 mol), in connection with the suppression of the FM phase as well as the enhancement of the resistivity. For x >= 0.4, gamma approaches to ~ 5 mJ/K^2 mol or less, where the antiferromagnetic order with an insulating feature in resistivity is generated. We suggest from these results that both disorder and reconstruction of the electronic states induced by doping Mn are coupled with the magnetic ground states and transport properties.
We investigated slow relaxations of the magnetostriction and residual magnetostriction of the phase-separated system (Eu$_{1-x}$Gd$_{x}$)$_{0.6}$Sr$_{0.4}$MnO$_3$, in which the metamagnetic transition from a paramagnetic insulating state to a ferromagnetic metallic state is accompanied by a lattice shrinkage. The relaxations are well fitted by a stretched exponential function, suggesting the strong frustraction between the double exchange interaction and Jahn-Teller effect. We have revealed that the Gd substitution suppresses the frozen phase-separated phase at low temperatures and stabilizes the paramagnetic insulating state in the dynamic phase-separated phase at intermediate temperatures. The former origin would be the randomness effect and the latter would be the suppression of the double exchange interaction.
We study and compare magnetic and electron paramagnetic resonance behaviors of bulk and nanoparticles of Nd(1-x)CaxMnO3 in hole doped (x = 0.4;NCMOH) and electron doped (x = 0.6;NCMOE) samples. NCMOH in bulk form shows a complex temperature dependence of magnetization M(T), with a charge ordering (CO) transition at around 250 K, an antiferromagnetic (AFM) transition at around 150 K and a transition to a canted AFM phase/mixed phase at around 80 K. Bulk NCMOE behaves quite differently with just a charge ordering transition at around 280 K, thus providing a striking example of the so called electron-hole asymmetry. While our magnetization data on bulk samples are consistent with the earlier reports, the new results on the nanoparticles bring out drastic effects of size reduction. They show that M(T) behaviors of the two nano samples are essentially similar in addition to the absence of the charge order in them thus providing strong evidence for vanishing of the electron-hole asymmetry in nanomanganites. This conclusion is further corroborated by electron paramagnetic resonance studies which show that the large difference in the g-values and their temperature dependence found for the two bulk samples disappears as they approach a common behavior in the corresponding nano samples.
Effects of x-ray irradiation on the crystal structure and the electrical resistance were examined at low temperatures for the insulating phase of spinel compound CuIr2S4. We found that the resistance decreases by more than five decades by irradiation at 8.5 K. The structural change from triclinic to tetragonal was observed at the same time. The x-ray-induced conductance is deduced to result from the destruction of Ir4+ dimers formed in the insulating phase. Slow relaxation of the resistance in the x-ray-induced state is also reported.
We investigate the effect of Ni${text -}$substitution on the crystalline structure and the critical behavior of $Nd_{0.6}Sr_{0.4}Mn_{1-x}Ni_{x}O_{3}$ (0.00 $leq$ x $leq$ 0.20) perovskite. X${text -}$ray diffraction patterns revealed that the major phase in all samples is the orthorhombic structure with space group $textit{Pnma}$. Rietveld refinement revealed a linear reduction in the lattice parameters along with monotonic reduction in the O2${text -}$Mn${text -}$O2 angel with increasing Ni concentration. The modified Arrott plots and the Kouvel${text -}$Fisher method have been used to analyze the magnetization isotherms near the paramagnetic to ferromagnetic (PM${text -}$FM) phase transition. The obtained critical exponents ($beta$, $gamma$ and $delta$) revealed that the Ni${text -}$free sample is consistent with 3D${text -}$Heisenberg like behavior. However, upon Ni${text -}$substitution, the critical exponents exhibit a mean field like behavior. The reliability of the obtained critical exponent ($beta$, $gamma$ and $delta$) values have been confirmed by the universal scaling behavior of the isothermal magnetization near the transition temperature.
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