Measurements of magnetoresistance and magnetization were carried out on ceramic samples of La0.5Pb0.5MnO3 and La0.5Pb0.5MnO3, containing 10 at. % Ag in a dispersed form. The results obtained for the resistivity at zero applied magnetic field exhibit a shallow minimum at the temperature T∼25–30 K which shifts towards lower temperatures upon applying a magnetic field and disappears at a certain field Hcr. Also the resistivity at helium temperature decreases upon applying magnetic fields. It is shown that the model of charge carriers tunneling between antiferromagnetically coupled grains may account for the results observed.
A slight minimum in the zero-field resistivity of a single crystalline La0.8Sr0.2MnO3 and shallow one for ceramic La0.8Sr0.2MnO3 samples were observed at T∼4 K and at T∼25–30 K, respectively. The minimum for the ceramic shifts towards lower temperatures, flattens with increasing magnetic fields (H), and vanishes at some critical H. The above effects are accompanied by an appreciable negative magnetoresistance (MR). On the other hand, the minimum for the single-crystalline sample is almost field independent and the MR in the relevant temperature range is very small. Two different mechanisms were found to account for the results observed in the single crystal and the polycrystalline samples: (i) mesoscopic corrections to the bulk resistivity that include Coulomb interaction and weak localization and (ii) intergranular tunneling. The resistivity of the large-grain ceramic sample comprises both types of behavior. The minimum of the bulk contribution becomes clearly seen under H, which suppresses the ceramic-type minimum.
Above the semiconductor-to-metallic transition (SMT) temperature (Tp), transport properties of the La1−xPbxMnO3+δ (0 ≤ x ≤ 0.5)-type mixed valence oxides with Tp between 230 and 275 K (depending on x) have been thoroughly examined for a small-polaron hopping conduction mechanism of the carriers. Although the variable range hopping (VRH) model was used earlier to fit the entire conductivity data above SMT, we noticed two distinct regions (above and below θD/2; θD is the Debye temperature) where different types of conduction mechanisms are followed. The high temperature (T > θD/2) conductivity data of all the Pb-doped samples follow the adiabatic hopping conduction mechanism, while those of LaMnO3 (x = 0) showing no SMT follow the non-adiabatic hopping conduction mechanism of Mott or Emin with reasonable values of polaron radius, hopping distance, polaron binding energy, activation energy, etc being different for different systems. The VRH model, however, fits the corresponding low temperature (T < θD/2) data of all the samples. Both resistivity ρ(T) and thermoelectric power S(T) follow a similar microscopic theory above Tp supporting the small-polaron hopping mechanism. Thermoelectric power also showed appreciable magnetic field dependence around SMT.
Neutron powder diffraction (NPD), ac susceptibility and electron magnetic resonance (EMR) techniques were employed for studying the crystallographic structure and magnetic ordering in CaMn 1−x Ru x O 3 ͑x ഛ 0.40͒ manganite system. It is shown that CaMn 1−x Ru x O 3 crystallizes in an orthorhombic Pnma perovskite structure within the temperature interval 1.5ഛ T ഛ 300 K independently on the level of Ru-doping ͑x͒. It means that the changes of the magnetic ordering in this system are solely determined by doping of Mn sites with Ru in parent CaMnO 3 compound. The NPD data show also that the long-ranged ferromagnetic (FM) ordering is developed in x ജ 0.10 compounds within antiferromagnetically (AFM) ordered matrix. The volume of this FM phase increases with x at the expense of the AFM one. The ac susceptibility ͑͒ demonstrates broadened peaks on ͑T͒ curves for x = 0.10, 0.15 samples and characteristic two-peak shape for x = 0.40 compound. The frequency dependence of ͑T͒ curves is also observed for x ജ 0.10 compounds. The complementary data of EMR indicate, in addition, the complex character of FM ordering, i.e., appearance of some nonequivalent FM phases, differ on its Curie temperatures and magnetocrystalline anisotropies in x ജ 0.15 samples. The best description of all these results could be done in the frame of the model of phase separated FMϩAFM ground state developing in the considered CaMn 1−x Ru x O 3 system for Ru concentrations x ജ 0.10.
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