No Arabic abstract
We investigate the behavior of ultrasharp metamagnetic transitions in La(5/8-y)Nd(y)Ca(3/8)MnO(3) manganites. These compounds change from a low temperature ferromagnetic metallic state at low Nd doping to a charge-ordered antiferromagnetic insulator for high Nd content. At an intermediate doping a phase-separated state is established. At low temperatures (2 K), we observe an avalanche-like field-induced metamagnetic transition, when the entire compound changes abruptly from one phase to the other. We investigate the signatures of this ultrasharp transition using magnetization and specific heat measurements. We observe a first order transition in the specific heat associated with discontinuous jumps in the magnetization. A strong increase of the sample temperature is simultaneously observed. The results are interpret in terms of latent heat release from the field induced enhancement of the ferromagnetic fraction, triggering the avalanche process.
We use femtosecond x-ray diffraction to study the structural response of charge and orbitally ordered Pr$_{1-x}$Ca$_x$MnO$_3$ thin films across a phase transition induced by 800 nm laser pulses. By investigating the dynamics of both superlattice reflections and regular Bragg peaks, we disentangle the different structural contributions and analyze their relevant time-scales. The dynamics of the structural and charge order response are qualitatively different when excited above and below a critical fluence $f_c$. For excitations below $f_c$ the charge order and the superlattice is only partially suppressed and the ground state recovers within a few tens of nanosecond via diffusive cooling. When exciting above the critical fluence the superlattice vanishes within approximately half a picosecond followed by a change of the unit cell parameters on a 10 picoseconds time-scale. At this point all memory from the symmetry breaking is lost and the recovery time increases by many order of magnitudes due to the first order character of the structural phase transition.
We report on the electronic and thermodynamic properties of the antiferromagnetic metal uranium mononitride with a Neel temperature $T_Napprox 53,$K. The fabrication of microstructures from single crystals enables us to study the low-temperature metamagnetic transition at approximately $58,$T by high-precision magnetotransport, Hall-effect, and magnetic-torque measurements. We confirm the evolution of the high-field transition from a broad and complex behavior to a sharp first-order-like step, associated with a spin flop at low temperature. In the high-field state, the magnetic contribution to the temperature dependence of the resistivity is suppressed completely. It evolves into an almost quadratic dependence at low temperatures indicative of a metallic character. Our detailed investigation of the Hall effect provides evidence for a prominent Fermi-surface reconstruction as the system is pushed into the high-field state.
The gigantic reduction of the electric resistivity under the applied magnetic field, CMR effect, is now widely accepted to appear in the vicinity of the insulator to metal transition of the perovskite manganites. Recently, we have discovered the first order transition from ferromagnetic metal to insulator in $rm La_{0.88}Sr_{0.12}MnO_3$ of the CMR manganite. This phase transition induces the tremendous increase of the resistivity under the external magnetic field just near above the phase transition temperature. We report here fairly detailed results from the systematic experiments including neutron and synchrotron X-ray scattering studies.
We present a study of the magnetocaloric effect in La5/8-yPryCa3/8MnO3 (y=0.3) and Pr0.5Ca0.09Sr0.41MnO3 manganites. The low temperature state of both ystems is the result of a competition between the antiferromagnetic and ferromagnetic phases. The samples display magnetocaloric effect evidenced in an adiabatic temperature change during a metamagnetic transition from an antiferromagnetic to a ferromagnetic phase . As additional features, La5/8-yPryCa3/8MnO3 exhibits phase separation characterized by the coexistence of antiferromagnetic and ferromagnetic phases and Pr0.5Ca0.09Sr0.41MnO3 displays inverse magnetocaloric effect in which temperature decreases while applying an external magnetic field. In both cases, a significant part of the magnetocaloric effect appears from non-reversible processes. As the traditional thermodynamic description of the effect usually deals with reversible transitions, we developed an alternative way to calculate the adiabatic temperature change in terms of the change of the relative ferromagnetic fraction induced by magnetic field. To evaluate our model, we performed direct measurement of the samples adiabatic temperature change by means of a differential thermal analysis. An excellent agreement has been obtained between experimental and calculated data. These results show that metamagnetic transition in manganites play an important role in the study of magnetic refrigeration.
We have investigated the metamagnetic-like transition in the triple layer ruthenate Sr4Ru3O10 by means of neutron diffraction from single crystals. The magnetic structure of the compound appears to be determined in a complex way by the two substructures of inequivalent ruthenium ions. At Tc=105K the system has a sharp transition into a ferromagnetic state along the c-axis which is driven by the ruthenium atoms in the central octahedra of the triple layers whereas the substructure of the outer ruthenium atoms tend to align in the ab plane achieving an antiferromagnetic order at the metamagnetic transition T*~50K. Below T* the strong anisotropy along c prevails, the outer ruthenium tend to align along the c-axis and the in-plane antiferromagnetic order disappears. This finding confirms the delicate balance between antiferro and ferromagnetic couplings in the (Sr,Ca)n+1RunO3n+1 family of compounds, and proves the layer dependence of the magnetic anisotropy in Sr4Ru3O10.