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Register a new userA critical examination of magnetic states of La$_{0.5}$Ba$_{0.5}$CoO$_3$: non-Griffiths phase and interacting ferromagnetic-clusters
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We report detailed dc magnetization, linear and non-linear ac susceptibility measurements on the hole doped disordered cobaltite La$_{0.5}$Ba$_{0.5}$CoO$_3$. Our results show that the magnetically ordered state of the system consists of coexisting non-ferromagnetic phases along with percolating ferromagnetic-clusters. The percolating ferromagnetic-clusters possibly undergo a 3D Hisenberg like magnetic ordering at the Curie temperature of 202(3) K. In between 202 and 220 K, the linear and non-linear ac susceptibility measurements show the presence of magnetic correlations even when the spontaneous magnetization is zero which indicates the presence of preformed short range magnetic-clusters. The characteristics of these short range magnetic-clusters that exist above Curie temperature are quite distinct than that of Griffiths phase e.g the inverse dc susceptibility exhibits an field independent upward deviation, and the second harmonic of ac susceptibility is non-negative. Below Curie temperature the system exhibit spin-glass like features such as irreversibility in the field cooled and zero field cooled magnetization and frequency dependence in the peak of ac susceptibility. The presence of a spin or cluster -glass like state is ruled out by the absence of field divergence in third harmonic of ac susceptibility and zero field cooled memory. This indicates that the observed spin-glass like features are possibility due to progressive thermal blocking of ferromagnetic-clusters which is further confirmed by the Wohlfarths model of superparamagnetism. The frequency dependence of the peak of ac susceptibility obeys the Vogel-Fulcher law with $tau_0approx 10^{-9}$ s. This together with the existence of an AT line in H-T space indicates the existence of significant inter-cluster interaction among these ferromagnetic-clusters.
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We report detailed dc magnetization, linear and non-linear ac susceptibility measurements on the hole doped disordered cobaltite La$_{0.5}$Ba$_{0.5}$CoO$_3$. Our results show that the magnetically ordered state of the system consists of coexisting non-ferromagnetic phases along with percolating ferromagnetic-clusters. The percolating ferromagnetic-clusters possibly start a magnetic ordering at the Curie temperature of 201.5(5)~K. The non-ferromagnetic phases mainly consist of antiferromagnetic-clusters with size smaller than the ferromagnetic-clusters. Below Curie temperature the system exhibits an irreversibility in the field cooled and zero field cooled magnetization and frequency dependence in the peak of ac susceptibility. These dynamical features indicate towards the possible coexistence of spin-glass phase along with ferromagnetic-clusters similar to La$_{1-x}$Sr$_{x}$CoO$_3$ (x$geq$0.18), but the absence of field divergence in third harmonic of ac susceptibility and zero field cooled memory clearly rule out any such possibility. We argue that the spin-glass phase in La$_{1-x}$Sr$_{x}$CoO$_3$ (x$geq$0.18) is associated with the presence of incommensurate antiferromagnetic ordering in non-ferromagnetic phases which is absent in La$_{0.5}$Ba$_{0.5}$CoO$_3$. Our analysis show that the observed dynamical features in La$_{0.5}$Ba$_{0.5}$CoO$_3$ are possibly due to progressive thermal blocking of ferromagnetic-clusters which is further confirmed by the Wohlfarths model of superparamagnetism. The frequency dependence of the peak of ac susceptibility obeys the Vogel-Fulcher law with $tau_0approx10^{-9}$s. This together with the existence of an AT line in H-T space indicates the presence of significant inter-cluster interaction among these ferromagnetic-clusters.
We have used high-resolution Extended X-ray Absorption Fine-Structure and diffraction techniques to measure the local structure of strained La$_{0.5}$Sr$_{0.5}$CoO$_3$ films under compression and tension. The lattice mismatch strain in these compounds affects both the bond lengths and the bond angles, though the larger effect on the bandwidth is due to the bond length changes. The popular double exchange model for ferromagnetism in these compounds provides a correct qualitative description of the changes in Curie temperature $T_C$, but quantitatively underestimates the changes. A microscopic model for ferromagnetism that provides a much stronger dependence on the structural distortions is needed.
We studied the charge-orbital ordering in the superlattice of charge-ordered insulating Pr$_{0.5}$Ca$_{0.5}$MnO$_3$ and ferromagnetic metallic La$_{0.5}$Sr$_{0.5}$MnO$_3$ by resonant soft x-ray diffraction. A temperature-dependent incommensurability is found in the orbital order. In addition, a large hysteresis is observed that is caused by phase competition between insulating charge ordered and metallic ferromagnetic states. No magnetic phase transitions are observed in contrast to bulk, confirming the unique character of the superlattice. The deviation from the commensurate orbital order can be directly related to the decrease of ordered-layer thickness that leads to a decoupling of the orbital-ordered planes along the c axis.
We report the magnetization study of the compound La$_{0.75}$Ba$_{0.25}$CoO$_3$ where Ba$^{2+}$ doping is just above the critical limit for percolation of ferromagnetic clusters. The field cooled (FC) and zero field cooled (ZFC) magnetization exhibit a thermomagnetic irreversibility and the ac susceptibility show a frequency dependent peak at the ferromagnetic ordering temperature (T$_C$$approx$203~K) of the clusters. These features indicate about the presence of a non-equilibrium state below T$_C$. In the non-equilibrium state, the dynamic scaling of the imaginary part of ac susceptibility and the static scaling of the nonlinear susceptibility clearly establish a spin-glass like cooperative freezing of ferromagnetic clusters at 200.9(2)~K. The existence of spin-glass like freezing of ferromagnetic clusters is further substantiated by the ZFC aging and memory experiments. We also observe certain dynamical features which are not present in a typical spin-glass, such as, initial magnetization after ZFC aging first increases and then decreases with the wait time and an imperfect recovery of relaxation in negative temperature cycling experiments. This imperfect recovery transforms to perfect recovery on concurrent field cycling. Our analysis suggests that these additional dynamical features have their origin in inter-cluster exchange interaction and cluster size distribution. The inter-cluster exchange interaction above the magnetic percolation gives a superferromagnetic state in some granular thin films but our results show the absence of typical superferromagnetic like state in La$_{0.75}$Ba$_{0.25}$CoO$_3$.
La$_{1.5}$Sr$_{0.5}$CoMn$_{0.5}$Fe$_{0.5}$O$_{6}$ (LSCMFO) compound was prepared by solid state reaction and its structural, electronic and magnetic properties were investigated. The material forms in rhombohedral $Rbar{3}c$ structure, and the presence of distinct magnetic interactions leads to the formation of a Griffiths phase above its FM transition temperature (150 K), possibly related to the nucleation of small short-ranged ferromagnetic clusters. At low temperatures, a spin glass-like phase emerges and the system exhibits both the conventional and the spontaneous exchange bias (EB) effects. These results resemble those reported for La$_{1.5}$Sr$_{0.5}$CoMnO$_{6}$ but are discrepant to those found when Fe partially substitutes Co in La$_{1.5}$Sr$_{0.5}$(Co$_{1-x}$Fe$_{x}$)MnO$_{6}$, for which the EB effect is observed in a much broader temperature range. The unidirectional anisotropy observed for LSCMFO is discussed and compared with those of resembling double-perovskite compounds, being plausibly explained in terms of its structural and electronic properties.
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