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Register a new userEnhanced grain surface effect on magnetic properties of nanometric La0.7Ca0.3MnO3 manganite : Evidence of surface spin freezing of manganite nanoparticles
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We have investigated the effect of nanometric grain size on magnetic properties of single phase, nanocrystalline, granular La0.7Ca0.3MnO3 (LCMO) sample. We have considered core-shell structure of our LCMO nanoparticles, which can explain its magnetic properties. From the temperature dependence of field cooled (FC) and zero-field cooled (ZFC) dc magnetization (DCM), the magnetic properties could be distinguished into two regimes: a relatively high temperature regime T > 40 K where the broad maximum of ZFC curve (at T = Tmax) is associated with the blocking of core particle moments, whereas the sharp maximum (at T = TS) is related to the freezing of surface (shell) spins. The unusual shape of M (H) loop at T = 1.5 K, temperature dependent feature of coercive field and remanent magnetization give a strong support of surface spin freezing that are occurring at lower temperature regime (T < 40 K) in this LCMO nanoparticles. Additionally, waiting time (tw) dependence of ZFC relaxation measurements at T = 50 K show weak dependence of relaxation rate [S(t)] on tw and dM/dln(t) following a logarithmic variation on time. Both of these features strongly support the high temperature regime to be associated with the blocking of core moments. At T = 20 K, ZFC relaxation measurements indicates the existence of two different types of relaxation processes in the sample with S(t) attaining a maximum at the elapsed time very close to the wait time tw = 1000 sec, which is an unequivocal sign of glassy behavior. This age-dependent effect convincingly establish the surface spin freezing of our LCMO nanoparticles associated with a background of superparamagnetic (SPM) phase of core moments.
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We report active control of the friction force at the contact between a nanoscale asperity and a La$_{0.55}$Ca$_{0.45}$MnO$_3$ (LCMO) thin film using electric fields. We use friction force microscopy under ultrahigh vacuum conditions to measure the friction force as we change the film resistive state by electric field-induced resistive switching. Friction forces are high in the insulating state and clearly change to lower values when the probed local region is switched to the conducting state. Upon switching back to an insulating state, the friction forces increase again. Thus, we demonstrate active control of friction without having to change the contact temperature or pressure. By comparing with measurements of friction at the metal-to-insulator transition and with the effect of applied voltage on adhesion, we rule out electronic excitations, electrostatic forces and changes in contact area as the reasons for the effect of resistive switching on friction. Instead, we argue that friction is limited by phonon relaxation times which are strongly coupled to the electronic degrees of freedom through distortions of the MnO6 octahedra. The concept of controlling friction forces by electric fields should be applicable to any materials where the field produces strong changes in phonon lifetimes.
The structure, electronic, and magnetic properties of the Mo-doped perovskite La0.7Ca0.3Mn1-xMoxO3 (x < 0.1) have been studied. A significant increase in resistivity and lattice parameters were observed with Mo doping. A marginal decrease in the Curie temperature Tc and the associated metal-insulator transition Tp were observed. Magnetization data reveal that long-range ferromagnetic ordering persists in all samples studied and the saturation moment decreases linearly as x increases. Enhancement in magnetoresistance at near Tc in the Mo-doped compounds with an optimum doping value x = 0.05 was observed. The overall experimental results can be explained by considering the induced Mn2+ ions with Mo6+ in the Mo-doped systems, with the strong FM coupling between Mn4+/2+- O - Mn3+.
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