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Register a new userSuppression of charge order and antiferromagnetic to ferromagnetic switchover in Nd_0.5 Ca_0.5 MnO_3 nanoparticles
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Nd_0.5 Ca_0.5 MnO_3 (NCMO) nanoparticles (average diameter ~ 20 and 40 nm) are synthesized by polymeric precursor sol-gel method and characterized by X- ray diffraction, transmission electron microscopy (TEM), selective area electron diffraction (SAED), superconducting quantum interference device (SQUID) magnetometery and resistivity measurements. Both single crystalline and polycrystalline particles are present in the samples and they are found to retain the orthorhombic structure of the bulk NCMO. However, most strikingly, in the 20 nm particles, the charge ordered (CO) and the antiferromagnetic phases observed in the bulk at 250 K and 160 K respectively are completely absent. Instead, a ferromagnetic (FM) transition is observed at 95 K followed by an insulator to metal transition at 75 K. In the 40 nm particles, though a weak, residual CO phase is observed, transition to FM state also occurs, but at a slightly higher temperature of 110 K. The magnetization is found to increase with the decrease of particle size.
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CaCo2As2 is a unique itinerant system having strong magnetic frustration. Here we report the effect of electron doping on the physical properties resulting from Ni substitutions for Co. The A-type antiferromagnetic transition temperature TN = 52 K for x = 0 decreases to 22 K with only 3 percent Ni substitution and is completely suppressed for x > 0.11. For 0.11 < x < 0.52 strong ferromagnetic (FM) fluctuations develop as revealed by magnetic susceptibility chi(T) measurements. Heat-capacity Cp(T) measurements reveal the presence of FM quantum spin fluctuations for 0.11 < x < 0.52. Our density-functional theory (DFT) calculations confirm that FM fluctuations are enhanced by Ni substitutions for Co. The Sommerfeld electronic heat-capacity coefficient is enhanced for x = 0, 0.21, and 0.42 by about a factor of two compared to DFT calculations of the bare density of states at the Fermi energy. The crystals with x > 0.52 do not exhibit FM spin fluctuations or magnetic order, which was found from the DFT calculations to arise from a Stoner transition. Neutron-diffraction studies of crystals with x = 0.11 and 0.16 found no evidence of A-type ordering as observed in CaCo2As2 or of other common magnetic structures.
Nanowires of Pr_0.57 Ca_0.41 Ba_0.02 MnO_3 (PCBM) (diameter ~ 80-90 nm and length ~ 3.5 mm) were synthesized by a low reaction temperature hydrothermal method. Single-phase nature of the sample was confirmed by XRD experiments. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to characterize the morphology and microstructures of the nanowires. While the bulk PCBM is known to exhibit charge order (CO) below 230 K along with a ferromagnetic transition at 110 K, SQUID measurements on the nanowires of PCBM show that the charge order is completely absent and a ferromagnetic transition occurs at 115 K. However, the magnetization in the nanowires is observed to be less compared to that in the bulk. This observation of the complete melting of the charge order in the PCBM nanowires is particularly significant in view of the observation of only a weakening of the CO in the nanowires of Pr_0.5 Ca_0.5 MnO_3. Electron paramagnetic resonance experiments were also carried out on the PCBM nanowires using an X-band EPR spectrometer. Characteristic differences were observed in the line width of nanowires when compared with that of the bulk.
Nanoparticles (dia ~ 5 - 7 nm) of Bi_0.5 X_0.5(X=Ca,Sr)MnO_3 are prepared by polymer assisted sol-gel method and characterized by various physico-chemical techniques. X-ray diffraction gives evidence for single phasic nature of the materials as well as their structures. Mono dispersed to a large extent, isolated nanoparticles are seen in the transmission electron micrographs. High resolution electron microscopy shows the crystalline nature of the nanoparticles. Superconducting quantum interferometer based magnetic measurements from 10 K to 300 K show that these nanomanganites retain the charge ordering (CO) nature unlike Pr and Nd based nanomanganites. The CO in Bi based manganites is thus found to be very robust consistent with the observation that magnetic field of the order of 130 T are necessary to melt the CO in these compounds. These results are supported by electron magnetic resonance measurements.
A lightly doped perovskite mangantite La_{0.88}Sr_{0.12}MnO_3 exhibits a phase transition at T_{OO}=145 K from a ferromagnetic metal (T_C=172 K) to a novel ferromagnetic insulator.We identify that the key parameter in the transition is the orbital degree of freedom in e_g electrons. By utilizing the resonant x-ray scattering technique, orbital ordering is directly detected below T_{OO}, in spite of a significant diminution of the cooperative Jahn-Teller distortion. The new experimental features are well described by a theory treating the orbital degree of freedom under strong electron correlation. The present experimental and theoretical studies uncover a crucial role of the orbital degree in the metal-insulator transition in lightly doped manganites.
X-ray scattering by multiferroic LuFe2O4 is reported. Below 320 K, superstructure reflections indicate an incommensurate charge order with propagation close to (1/3,1/3,3/2). The corresponding charge configuration, also found by electronic structure calculations as most stable, contains polar Fe/O double-layers with antiferroelectric stacking. Diffuse scattering at 360 K, with (1/3,1/3,0) propagation, indicates ferroelectric short-range correlations between neighboring double-layers. The temperature dependence of the incommensuration indicates that charge order and magnetism are coupled.
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