No Arabic abstract
We have thoroughly investigated the entire magnetic states of under doped ferromagnetic insulating manganite Nd0.8Sr0.2MnO3 through temperature dependent linear and non linear complex ac magnetic susceptibility measurements. This ferromagnetic insulating manganite is found to have frequency independent ferromagnetic to paramagnetic transition temperature at around 140 K. At around 90 K (approx T_f) the sample shows a second frequency dependent re - entrant magnetic transition as explored through complex ac susceptibility measurements. Non linear ac susceptibility measurements (higher harmonics of ac susceptibility) have also been performed (with and without the superposition of a dc magnetic field) to further investigate the origin of this frequency dependence (dynamic behavior at this re-entrant magnetic transition). Divergence of 3rd order susceptibility in the limit of zero exciting field indicates a spin glass like freezing phenomena. However, large value of spin relaxation time (?0= 10-8 s) and small value of coercivity (~22 Oe) obtained at low temperature (below T_f) from critical slowing down model and dc magnetic measurements, respectively, are in contrast with what generally observed in a canonical spin glass (?0 = 10-12 - 10-14 s and very large value of coercivity below freezing temperature). We have attributed our observation to the formation of finite size ferromagnetic clusters which are formed as consequence of intrinsic separation and undergo cluster glass like freezing below certain temperature in this under doped manganite. The results are supported by the electronic - and magneto - transport data.
The self-organization of strongly interacting electrons into superlattice structures underlies the properties of many quantum materials. How these electrons arrange within the superlattice dictates what symmetries are broken and what ground states are stabilized. Here we show that cryogenic scanning transmission electron microscopy enables direct mapping of local symmetries and order at the intra-unit-cell level in the model charge-ordered system Nd$_{1/2}$Sr$_{1/2}$MnO$_{3}$. In addition to imaging the prototypical site-centered charge order, we discover the nanoscale coexistence of an exotic intermediate state which mixes site and bond order and breaks inversion symmetry. We further show that nonlinear coupling of distinct lattice modes controls the selection between competing ground states. The results demonstrate the importance of lattice coupling for understanding and manipulating the character of electronic self-organization and highlight a novel method for probing local order in a broad range of strongly correlated systems.
A universal linear-temperature dependence of the uniform magnetic susceptibility has been observed in the nonmagnetic normal state of iron-pnictides. This non-Pauli and non-Curie-Weiss-like paramagnetic behavior cannot be understood within a pure itinerant picture. We argue that it results from the existence of a wide antiferromagnetic fluctuation window in which the local spin-density-wave correlations exist but the global directional order has not been established yet.
The low temperature lattice structure and magnetic properties of Co$_{2.75}$Fe$_{0.25}$O$_4$ ferrite have been investigated using experimental results from synchrotron x-ray diffraction (SXRD), dc magnetization, ac susceptibility, neutron diffraction and neutron depolarization techniques. The samples have been prepared by chemical co-precipitation of the Fe and Co nitrates solution in high alkaline medium and subsequent thermal annealing of the precipitates in the temperature range of 200- 900 $^circ$C. Rietveld refinement of the SXRD patterns at room temperature indicated two-phased cubic spinel structure for the samples annealed at temperatures 200-600 $^circ$C. The samples annealed at temperatures 700 $^circ$C and 900 $^circ$C (CF90) have been best fitted with single phased lattice structure. Refinement of the neutron diffraction patterns in the temperature range of 5-300 K confirmed antiferromagnetic (AFM) Co$_3$O$_4$ and ferrimagnetic (FIM) Co$_{2.75}$Fe$_{0.25}$O$_4$ phases for the sample annealed at 600 $^circ$C and single FIM phase of Co$_{2.75}$Fe$_{0.25}$O$_4$ for the CF90 sample. Magnetic measurements have shown a non-equilibrium magnetic structure, consisting of the high temperature FIM phase and low temperature AFM phase. The magnetic phases are sensitive to magnetic fields, where high temperature phase is suppressed at higher magnetic fields by enhancing the low temperature AFM phase, irrespective of annealing temperature of the samples.
UCoGe is one of the few compounds showing the coexistence of ferromagnetism and superconductivity at ambient pressure. With T_Curie = 3 K and T_SC = 0.6 K it is near a quantum phase transition; the pressure needed to suppress the magnetism is slightly higher than 1 GPa. We report simultaneous resistivity and ac-susceptibility measurements under pressure on a polycrystal with very large single-crystalline domains and a resistivity ratio of about 6. Both methods confirm the phase diagram established before by resistivity measurements on a polycrystal. The ferromagnetic phase is suppressed for P approximately 1.2 GPa. Astonishingly, the superconductivity persists at pressures up to at least 2.4 GPa. In other superconducting and ferromagnetic heavy fermion compounds like UGe2 and URhGe, the superconducting state is situated only inside the larger ferromagnetic region. Therefore, UCoGe seems to be the first example where superconductivity extends from the ferromagnetic to the paramagnetic region.
Calcium ruthenate ($CaRuO_3$) is widely believed to be located close to a quantum critical point due to the strong non-Fermi-liquid behavior expressed in the temperature dependence of electronic transport, specific heat, optical conductivity, etc. However, the corresponding anomalous behavior, marking crossover temperature regimes in the magnetic response of $CaRuO_3$, is still lacking. Here we report detailed AC and DC magnetic susceptibility measurements of $CaRuO_3$ and $CaRu_{0.97}Ti_{0.03}O_3$. The AC magnetic susceptibility measurements of the $CaRuO_3$ show a slight dependence on the frequency of AC magnetic field below ~ 40 K, and an additional subtle change of curvature around 12 K. We interpret these results as a critical slowing down of spin fluctuations towards T=0 K. We confirm these observations by magnetic measurements of $CaRu_{0.97}Ti_{0.03}O_3$, which show a pronounced magnetic response corresponding to the above temperatures.