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تسجيل مستخدم جديدThe effects of Co3O4 on the Structure and Unusual Magnetism of LaCoO3
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Bulk La_wCoO3 particles with w=1.1, 1.0, 0.9, 0.8, and 0.7 were synthesized using starting materials with varying molar ratios of La2O3 and Co3O4. The resulting particles are characterized as LaCoO3 crystals interfaced with a crystalline Co3O4 phase. X-ray and neutron scattering data show little effect on the average structure and lattice parameters of the LaCoO3 phase resulting from the Co3O4 content, but magnetization data indicate that the amount of Co3O4 strongly affects the ferromagnetic ordering at the interfaces below T_C ~89K. In addition to ferromagnetic long-range order, LaCoO3 exhibits antiferromagnetic behavior with an unusual temperature dependence. The magnetization for fields 20 Oe < H < 5 kOe is fit to a combination of a power law ((T-T_C)/T_C)^beta behavior representing the ferromagnetic long-range order and sigmoid-convoluted Curie-Weiss-like behavior representing the antiferromagnetic behavior. The critical exponent beta=0.63 +- 0.02 is consistent with 2D (surface) ordering. Increased Co3O4 correlates well to increased ferromagnetism. The weakening of the antiferromagnetism below T ~ 40K is a consequence of the lattice reaching a critical rhombahedral distortion as T is decreased for core regions far from the Co3O4 interfaces. We introduce a model that describes the ferromagnetic behavior of the interface regions and the unusual antiferromagnetism of the core regions.
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Bulk and nanoparticle powders of LaCoO3 (LCO) were synthesized, and their magnetic and structural properties were studied using SQUID magnetometry and neutron diffraction. The bulk and large nanoparticles exhibit weak ferromagnetism (FM) below T ~ 85
K and a crossover from strong to weak antiferromagnetic (AFM) correlations near a transition expressed in the lattice parameters, To ~ 40K. This crossover does not occur in the smallest nanoparticles; instead, the magnetic behavior is predominantly ferromagnetic. The amount of FM in the nanoparticles depends on the amount of Co3O4 impurity phase, which induces tensile strain on the LCO lattice. A core-interface model is introduced, with the core region exhibiting the AFM crossover and with FM in the interface region near surfaces and impurity phases.
LaCoO3 (LCO) nanoparticles were synthesized and their magnetic and structural properties were examined using SQUID magnetometery and neutron diffraction. The nanoparticles exhibit ferromagnetic long-range order beginning at T_C approximately 87K that
persists to low temperatures. This behavior is contrasted with the ferromagnetism of bulk LCO, which also starts at T_C approximately 87K but is suppressed below a second transition at T_o approximately 37K, due to a structural phase transition. The ferromagnetism in both systems is attributed to the tensile stress from particle surfaces and impurity phase interfaces. This stress locally increases the Co-O-Co bond angle gamma, and competes with the thermal contraction of the lattice. It has recently been shown that LCO loses long-range ferromagnetic order when gamma decreases below the critical value gamma_c = 162.8 degrees. Consistent with this model, we show that gamma in nanoparticles remains larger than gamma_c at low temperatures, likely a consequence of all spins being in close proximity to surfaces or interfaces.
We investigate the structure and magnetic properties of thin films of the LaCoO$_{3}$ compound. Thin films are deposited by pulsed laser deposition on various substrates in order to tune the strain from compressive to tensile. Single-phase (001) orie
nted LaCoO$_{3}$ layers were grown on all substrates despite large misfits. The tetragonal distortion of the films covers a wide range from -2% to 2.8%. Our LaCoO$_{3}$ films are ferromagnetic with Curie temperature around 85 K, contrary to the bulk. The total magnetic moment is below $1mu_{B}$/Co$^{3+}$, a value relatively small for an exited spin-state of the Co$^{3+}$ ions, but comparable to values reported in literature. A correlation of strain states and magnetic moment of Co$^{3+}$ ions in LaCoO$_{3}$ thin films is observed.
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tice distortion from the cubic spinel to a tetragonal I41/amd lattice below TN = 21 K, where powder neutron diffraction confirms the formation of a helical magnetic structure with magnetic moment of 3.04(3) {mu}B at 1.5 K; close to that expected for high-spin Cr3+. MuSR measurements show prominent local spin correlations that are established at temperatures considerably higher (< 100 K) than the onset of long range magnetic order. The stretched exponential nature of the relaxation in the local spin correlation regime suggests a wide distribution of depolarizing fields. Below TN, unusually fast (> 100 {mu}s-1) muon relaxation rates are suggestive of rapid site hopping of the muons in static field. Inelastic neutron scattering measurements show a gapless mode at an incommensurate propagation vector of k = (0 0 0.4648(2)) in the low temperature magnetic ordered phase that extends to 0.8 meV. The dispersion is modelled by a two parameter Hamiltonian, containing ferromagnetic nearest neighbor and antiferromagnetic next nearest neighbor interactions with a Jnnn/Jnn = -0.337.
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ron correlation strength, U. In addition to the correlation effect, spin-orbit interaction is observed to play a significant role in the case of intermediate spin and high spin configurations. The comparison of the calculated Co 3d and O 2p partial density of states with the experimental valence band spectra indicates that at room temperature, Co has dominant intermediate spin state configuration and that the high spin configuration may not be significant at this temperature. The lineshape of the La 5p and O 2s core level spectra could be reproduced well within these ab initio calculations.
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