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Register a new userMagnetocaloric effect in nano- and polycrystalline manganite $La_{0.7}Ca_{0.3}MnO_3$
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$La_{0.7}Ca_{0.3}MnO_3$ samples were prepared in nano- and polycrystalline forms by sol-gel and solid state reaction methods, respectively, and structurally characterized by synchrotron X-ray diffraction. The magnetic properties determined by ac susceptibility and dc magnetization measurements are discussed. The magnetocaloric effect in this nanocrystalline manganite is spread over a broader temperature interval than in the polycrystalline case. The relative cooling power of the poly- and nanocrystalline manganites is used to evaluate a possible application for magnetic cooling below room temperature.
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In order to analyse the effect of strain on the magnetic properties of narrow-band manganites, the temperature and field dependent susceptibilities of about 8.5 nm thick epitaxial Pr0.7Ca0.3MnO3 films, respectively grown on (001) and (110) SrTiO3 substrates, have been compared. For ultrathin samples grown on (001) SrTiO3, a bulk-like cluster-glass magnetic behaviour is found, indicative of the possible coexistence of antiferromagnetic and ferromagnetic phases. On the contrary, ultrathin films grown on (110) substrates show a robust ferromagnetism, with a strong spontaneous magnetization of about 3.4 mB /Mn atom along the easy axis. On the base of high resolution reciprocal space mapping analyses performed by x-ray diffraction, the different behaviours are discussed in terms of the crystallographic constraints imposed by the epitaxy of Pr0.7Ca0.3MnO3 on SrTiO3. We suggest that for growth on (110) SrTiO3, the tensile strain on the film c-axis, lying within the substrate plane, favours the ferromagnetic phase, possibly by allowing a mixed occupancy and hybridization of both in-plane and out-of-plane eg orbitals. Our data allow to shed some physics of inhomogeneous states in manganites and on the nature of their ferromagnetic insulating state.
Large magnetoresistive materials are of immense interest for a number of spintronic applications by developing high density magnetic memory devices, magnetic sensors and magnetic switches. Colossal magnetoresistance, for which resistivity changes several order of magnitude (${sim10^4 %}$) in an external magnetic field, occurs mainly in phase separated oxide materials, namely manganites, due to the phase competition between the ferromagnetic metallic and the antiferromagnetic insulating regions. Can one further enhance the magnetoresistance by tuning the volume fraction of the two phases? In this work, we report a huge colossal magnetoresistance along with the ultra-sharp metamagnetic transition in half doped ${Sm_{0.5}Ca_{0.25}Sr_{0.25}MnO_3}$ manganite compound by suitably tuning the volume fraction of the competing phases. The obtained magnetoresistance value at 10 K is as large as $sim10^{13}%$ in a 30 kOe external magnetic field and $sim10^{15}%$ in 90 kOe external magnetic field and is several orders of magnitude higher than any other observed magnetoresistance value reported so far. Using model Hamiltonian calculations we have shown that the inhomogeneous disorder, deduced from tunneling electron microscopy, suppresses the CE-type phase and seeds the ferromagnetic metal in an external magnetic field.
We report a detailed study of the electric transport and magnetic properties of the LaNdCaMnO manganite system. Substitution of LaIII by smaller NdIII ions, reduces the mean ionic radius of the A site ion. We have studied samples in the entire range between rich La and rich Nd compounds. Results of DC magnetization and resistivity show that doping destabilize the FM character of the pure La compound and triggers the formation of a phase separated state at intermediate doping. We have also found evidence of a dynamical behaviour within the phase separated state. A phase diagram is constructed, summarizing the effect of chemical substitution on the system.
We investigate the ultra-sharp jump in the isothermal magnetization and the resistivity in the polycrystalline $Sm_{0.5}(Ca_{0.5-y}Sr_{y})MnO_3$ $(y = 0, 0.1, 0.2, 0.25, 0.3, 0.5)$ compounds. The critical field $(H_{cr})$, required for the ultra-sharp jump, decreases with increase of `Sr concentration, i.e. with increase of average A-site ionic radius $langle r_Arangle$. The magnetotransport data indicate that the phase separation increases with the increase of $langle r_Arangle$, i.e. with $y$. The dependency of $H_{cr}$ with magnetic field sweep rate reveals that the ultra-sharp jump from antiferromagnetic (AFM) state to the ferromagnetic (FM) state is of martensitic in nature. Our two-band double exchange model Hamiltonian calculations show that the `Sr doping induces the ferromagnetic clusters in the antiferromagnetic insulating phase and in turn reduces the critical field. In the end we present a phenomenological picture obtained from our combined experimental and theoretical study.
Some possible connection between spin and charge degrees of freedom in magneto-resistive manganites is investigated through a thorough experimental study of the magnetic (AC susceptibility and DC magnetization) and transport (resistivity and thermal conductivity) properties. Measurements are reported in the case of well characterized polycrystalline La_{0.8}Sr_{0.2}MnO_3 samples. The experimental results suggest rather strong field-induced polarization effects in our material, clearly indicating the presence of ordered FM regions inside the semiconducting phase. Using an analytical expression which fits the spontaneous DC magnetization, the temperature and magnetic field dependences of both electrical resistivity and thermal conductivity data are found to be well reproduced through a universal scenario based on two mechanisms: (i) a magnetization dependent spin polaron hopping influenced by a Zeeman splitting effect, and (ii) properly defined thermally excited polaron states which have to be taken into account in order to correctly describe the behavior of the less conducting region. Using the experimentally found values of the magnetic and electron localization temperatures, we obtain L=0.5nm and m_p=3.2m_e for estimates of the localization length (size of the spin polaron) and effective polaron mass, respectively.
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