Effects of Particle Size on Electromagnetic and Microwave Absorption Properties of La0.7Sr0.3MnO3±δ‐Epoxy Composite

La_0.7Sr_0.3MnO_3±δ powders were fabricated by solid‐state reaction method at 1473 K for 4 h. The precursors were prepared by ball‐milling raw materials for 3, 6, 9, and 12 h, respectively. The crystal structures, particle size, and morphologies of precursors and prepared La_0.7Sr_0.3MnO_3±δ were characterized by XRD, laser particle size analyzer and SEM, respectively. It is found that La_0.7Sr_0.3MnO_3±δ possessed large particle size by ball‐milling raw materials for a long time. Results indicated that La_0.7Sr_0.3MnO_3±δ, synthesized by ball‐milling raw materials for 3 h, exhibited the optimal microwave absorption properties. The maximum reflection loss was ?28.8 dB, and the ?6 dB absorption bandwidth was 5.80 GHz.     

Influence of Ce addition on the structural,magnetic, and magnetocaloric properties in La0.7−xCexSr0.3MnO3 (0≤x≤0.3) ceramic compound

We report improvement in the magnetocaloric properties of Ce-doped lanthanum manganites. Polycrystalline La_0.7−xCe_xSr_0.30MnO₃ (0≤x≥0.3) samples were prepared using the conventional solid-state reaction method with phase purity and structure confirmed using X-ray diffraction. Temperature dependent magnetization measurements and Arrott analysis reveal second order ferromagnetic transition in parent sample and as well as in doped sample with Curie temperature decreasing progressively with increasing Ce-concentration from ~370 K for x=0.0 to 310 K for x=0.30. Magnetic entropy change (ΔS_M) was calculated by applying the thermodynamic Maxwell equation to a series of isothermal field dependent magnetization curves. A large ΔS_M associated with the ferromagnetic–paramagnetic transition in La_0.7−xCe_xSr_0.30MnO₃ samples has been observed. The value of ΔS_M was found to increase with Ce-doping up to x=0.15 and the highest value of 2.12 J kg⁻¹ K⁻¹ (at ΔH=2 T) was observed for La_0.55Ce_0.15Sr_0.30MnO₃ sample near the Curie temperature of 356 K. Also, improved relative cooling power of ~122 J kg⁻¹ was observed for the same sample. Due to the large magnetic entropy change and high Curie temperature, the La_0.55Ce_0.15Sr_0.30MnO₃ sample is suggested to be used as potential magnetic refrigerants for magnetic refrigeration technology above room temperature.     

Investigation of structural,optical, electrical,and magnetic properties of Fe-doped La0.7Sr0.3MnO3 manganites

In this work, the physical properties of nanocrystalline samples of La_0.7Sr_0.3Mn_1−xFe_xO₃ (0.0 ≤ x ≤ 0.20) perovskite manganites synthesized by the reverse micelle (RM) technique were explored in detail. The phase purity, crystal structure, and crystallite size of the samples were determined using X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. All the samples had rhombohedral crystal structure and crystallite size increased with increase in Fe content in La_0.7Sr_0.3MnO₃. The scanning electron micrographs (SEMs) exhibited smooth surface morphology and nonuniform shape of the particles. The optical properties studied using UV-visible absorption spectroscopy revealed a decrease in the absorbance and optical band gap with an increase in Fe content in La_0.7Sr_0.3MnO₃ compound. The temperature-dependent resistivity measurements revealed semiconducting nature of x = 0 and 0.1 samples up to the studied temperature range, while a metal-to-insulator transition was observed at higher Fe doping. Magnetic studies revealed weak ferromagnetism in all the samples and a reduction in the maximum magnetization with an increase in Fe content. A close correlation between electrical transport and magnetic properties was observed with the doping of Fe ion in La_0.7Sr_0.3MnO₃ at Mn site. These results advocate strong interactions associated with the double exchange mechanism among Fe³⁺ and Mn³⁺ ions.     

Room-temperature large magnetocaloric effect and critical behavior in La0.6Dy0.1Sr0.3MnO3

The effect of dysprosium incorporation in La_0.7Sr_0.3MnO₃ perovskite manganite on its magnetic properties, magnetocaloric effect and critical behavior was investigated. The temperature dependent magnetization data exhibit a sharp paramagnetic–ferromagnetic transition at T_C=307 K, which nature has been identified to be a second-order transition by the scaling laws for magnetocaloric effect. The maximum magnetic entropy change and the relative cooling power are found to be, respectively, 8.314 J/kg K and 187 J/kg for a 5 T magnetic field change without a hysteresis loss, making this material a promising candidate for magnetic refrigeration at room temperature. To study the critical behavior of the paramagnetic–ferromagnetic transition, some related critical exponents (β, γ, and δ) have been also calculated. The values of critical exponents indicate that the present phase transition does not belong to the common transition classes but shows some abnormal variation. We suggest that the induced lattice disordering and magnetic disordering due to Dysprosium incorporation are essential reasons for the presence of a large magnetocaloric effect and of an anomalous ferromagnetic phase transition in the present material     

Modified self-propagating high-temperature synthesis of nanosized La0.7Ca0.3MnO3

A modified solid-state combustion route was developed for the preparation of nanocrystalline manganite La_0.7Ca_0.3MnO₃ in a single-step process, using metal nitrates and glucose/KNO₃ redox mixture. The obtained sample was found to crystallize within O′ type of orthorhombic perovskite structure (space group Pnma), without the presence of other structural phases or impurities. Nanoparticles are found to have particle size in the range 12–35 nm, and to be highly crystalline without the presence of amorphous surface layer. Magnetic measurements show that nanoparticles display bulk-like magnetic properties, with ferromagnetic phase transition at 125 K and the absence of superparamagnetic or spin-glass behavior.     

Magnetic properties of La0.7Sr0.3MnO3 under the pressure and the transport property under the magnetic field

Polycrystalline La_0.7Sr_0.3MnO₃ sample (LSMO) was synthesized by the solid phase reaction; it exhibits the paramagnetic-ferromagnetic transition at T_c = 362 K at the ambient pressure; it is paramagnetic metallic state above T_c and the ferromagnetic metallic state below T_c. It was observed that the pressure effect depends on the temperature range: (a) In the paramagnetic region, the magnetization M hardly changes with the pressure P, that is, ΔM≈0. There exist the antiferromagnetic (AFM) coupled ferromagnetic clusters in the paramagnetic region, and the pressure enhances the AFM coupling. (b) In the temperature range around T_c, the pressure increases M, that is, ΔM > 0, with the concomitant increase in T_c; the average pressure coefficient dT_c/dP is 5.40 K/GPa at P = .74 GPa, much smaller than 15.47 and 15.90 K/GPa for La_0.7Ca_0.3MnO₃ and La_0.9Ca_0.1MnO₃, respectively, due to the different distortion degree of MnO₆ octahedra in Ca and Sr doped manganites. (c) In the temperature region below T_c, the pressure reduces M, that is, ΔM < 0. M is determined by the competition between the Mn³⁺-O-Mn⁴⁺ double exchange and the interparticle dipolar interaction. The pressure enhances the interparticle dipolar interaction, leading to a significant decrease in magnetization. The resistivity of LSMO exhibits the metallic behavior in the temperature range of 5 K~370 K; it decreases as the applied magnetic field H increases from 0 to 7 T, that is, the magnetoresistance effect which is more significant around T_c. The fitting to the low-temperature resistivity shows that the applied magnetic field reduces the scattering from the grain boundary, electron, phonon, and magnon, especially reduces the electron-electron scattering.     

Large increase of Curie temperature in (110)-oriented La0.7Sr0.3MnO3 films

From the perspectives of scientific researches and practical applications, it is desirable to explore high operating temperature ferromagnetic films. The effect of biaxial strain on magnetic properties of (110)-oriented La_0.7Sr_0.3MnO₃ films was studied. High quality La_0.7Sr_0.3MnO₃ films were grown on (110)-oriented perovskite single crystal substrates using pulsed laser deposition, varying substrate-induced misfit strains from ??2.27–0.75%. A remarkable enhancement of Curie temperature has been achieved for (110)-oriented La_0.7Sr_0.3MnO₃ films clamped with small misfit strains (i.e., grown on LAST (110)). The enhanced Curie temperature of (110)-oriented La_0.7Sr_0.3MnO₃ films could be attributed to the misfit strain between the films and the underlying substrates and may have technological implication for applications at high temperature environments.     

Structural,morphological, and magnetic properties of sol-gel derived La0.7Ca0.3MnO3 manganite nanoparticles

La_0.7Ca_0.3MnO₃ (LCMO) manganite nanoparticles are synthesized via a sol-gel route at different annealed temperatures. Their structural, morphological, and magnetic properties are investigated. The X-ray diffraction patterns coupled with electron diffraction confirm that all the LCMO samples are single phase and crystallize in the orthorhombic perovskite structure (Pnma space group). The morphology of the samples observed by TEM, reveals a spherical shape with an average grain size lower than 50 nm. The resolved lattice fringes in high-resolution TEM images also reveal the single crystalline nature of the LCMO nanoparticles. Magnetization measurements versus temperature under low magnetic field (0.01 T) show a paramagnetic - ferromagnetic transition for all the samples. The Curie temperature (T_c) is found to be decreased with increasing the annealed temperature. A bifurcation is observed in the zero field-cooled and field-cooled magnetizations, indicating a competition between ferromagnetic and antiferromagnetic interactions in the nanoparticles at low temperatures. Field-cooled hysteresis measurements suggest a cluster glasslike behavior of the nanoparticles. Room temperature and low temperature M - H loops demonstrate that all the samples exhibit ferromagnetic behavior at 5 K, whereas a paramagnetic behavior at room temperature. Resistivity behavior of the LCMO samples shows that they exhibit a metal - insulator transition. Magnetoresistance of ~ 50% at the field up to 8 T was observed at 2 K in the LSCO samples annealed at 600 °C.     

Structure and properties of (1-x)La0.67Sr0.33MnO3/xMnOδ multicomponent composite

(1-x)La_0.67Sr_0.33MnO₃/xMnO_δ [(1-x)LSMO/xMnO_δ] multicomponent composites were prepared. Their structure and properties were investigated as function of composition. X-ray diffraction and x-ray photoelectron spectroscopy confirmed the coexistence of MnO, Mn₂O₃ and MnO₂. It was found that MnO_δ introduction led to decreased average grain size and metal-insulator transition temperature. But it can increase maximum resistivity and magnetoresistance. The corresponding values were 2.0 μm, 370 K, 0.017 Ω cm, −24.7% (10 K, 2 T) for x = 0 and 0.7 μm, 225 K, 1.899 Ω cm and −25.6% (10 K, 2 T) for x = 0.3. However, the ferromagnetic Curie temperature was almost composition-independent with the value of 305 K. These results indicate that forming multicomponent composite by introducing ferromagnetic second phases can suppress the drawbacks of conventional ferromagnetic materials.     

Structural,magnetic and magnetocaloric study of La0.7−xEuxSr0.3MnO3 (x=0.1, 0.2 and 0.3) manganites

This paper reports the structural, magnetic and magnetocaloric properties of La_0.7−xEu_xSr_0.3MnO₃ (x=0.1, 0.2 and 0.3) polycrystalline manganites elaborated using the solid-state reaction at high temperatures. The X-ray powder diffraction shows that all the prepared compounds are single phase. La_0.6Eu_0.1Sr_0.3MnO₃ is crystallized in the rhombohedral symmetry, whereas a structural transition towards orthorhombic system is observed for x≥0.2. Eu doping was found to induce a decrease of the Curie temperature T_C from 343 K (x=0.1) to 272 K (x=0.3). All compounds undergo a large magnetocaloric effect and have consequently potential applications in magnetic refrigeration domain around room temperature.     

Synthesis of La0.7Sr0.3MnO3 at 800 °C using citrate gel method

Manganite systems have been of considerable interest in the recent past due to their potential to operate in wide property range and also to serve as effective magnetic sensing and storing devices when synthesized using stringent conditions. We report a novel citrate gel method, in which La_0.7Sr_0.3MnO₃ system has been synthesized at temperature 800 °C (LSMO800) with the synthesis duration is 6 h. The results have been compared with the sample synthesized at 1050 °C (LSMO1050). The synthesized bulk polycrystalline sample shows single-phase nature with the increase in particle size from ∼50 nm to 300 nm with the increase in the sintering temperature. The magnetization data for LSMO800 shows well-defined hysteresis with saturation magnetization at around 1800 Oe and Curie temperature at 360 K, which is slightly lower than that of LSMO1050, which is 375 K. The results can be well attributed to the grain boundary effects.     

Enhanced Microwave Absorption Properties of Intrinsically Core/shell Structured La0.6Sr0.4MnO3 Nanoparticles

The intrinsically core/shell structured La_0.6Sr_0.4MnO₃nanoparticles with amorphous shells and ferromagnetic cores have been prepared. The magnetic, dielectric and microwave absorption properties are investigated in the frequency range from 1 to 12 GHz. An optimal reflection loss of −41.1 dB is reached at 8.2 GHz with a matching thickness of 2.2 mm, the bandwidth with a reflection loss less than −10 dB is obtained in the 5.5–11.3 GHz range for absorber thicknesses of 1.5–2.5 mm. The excellent microwave absorption properties are a consequence of the better electromagnetic matching due to the existence of the protective amorphous shells, the ferromagnetic cores, as well as the particular core/shell microstructure. As a result, the La_0.6Sr_0.4MnO₃nanoparticles with amorphous shells and ferromagnetic cores may become attractive candidates for the new types of electromagnetic wave absorption materials.     

Spin dependent transport at oxide La0.7Ca0.3MnO3/YBa2Cu3O7 ferromagnet/superconductor interfaces

We have found large magnetoresistance in ferromagnet/superconductor/ferromagnet heterostructures made of La_0.7Ca_0.3MnO₃ and YBa₂Cu₃O₇. It originates at an increase of the width of the resistive transition when the magnetizations of the ferromagnetic layers are aligned antiparallel. We find that the shape and height of the magnetoresistance peaks are not modified when the angle between current and magnetic field is changed from parallel or perpendicular. Furthermore, we find that the temperature shift of the resistance curves is independent of the current values. This favors the view that the magnetoresistance phenomenon originates at the spin dependent transport of quasiparticles transmitted from the ferromagnetic electrodes into the superconductor, and rules out interpretations in terms of spontaneous vortices or anisotropic magnetoresistance of the ferromagnetic layers.     

The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries

Cathodic material for sodium-ion rechargeable batteries based on Na_xMnO₂ were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na_0.7MnO_2.05 nanoplates were obtained at 850 °C, while 3-D tunnel structured Na_0·4MnO₂ and Na_0·44MnO₂, both with rod-like morphology, were obtained at 800 °C and 900 °C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO₃ solution have shown that Na_0·44MnO₂ obtained at 900 °C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.     

Electrical transport properties of Sm-doped La0.7Ca0.3MnO3 polycrystalline ceramics

Improving the magnetoresistance effect of perovskite ceramic materials under a low applied magnetic field to expand its application range is one of the main research directions of this type of material. In this study, La_0.7Ca_0.3MnO₃ was doped with different levels of Sm by the sol-gel method to yield a series of La_0.7-xSm_xCa_0.3MnO₃ (LSCMO) polycrystalline ceramics. X-ray diffraction (XRD) results revealed that LSCMO ceramics possessed standard perovskite structures. Scanning electron microscopy (SEM) showed grains closely connected without obvious holes. In addition, the grain size gradually decreased with the increase in Sm doping content. The resistivity temperature curves displayed a clear metal-insulator transition behavior of LSCMO accompanied by a steep change from ferromagnetic to paramagnetic behavior (FM-PM). The metal-insulator transition temperature (T_p) values of the as-obtained LSCMO gradually shifted toward lower temperatures with increase in Sm content. Moreover, resistivity temperature coefficient (TCR) and magnetoresistance (MR) values also gradually increased with Sm doping content. The transport properties in polycrystalline ceramics could be adequately explained by the double exchange model, which would be useful for interpreting the CMR effects when used in magnetic devices.     

Effect of microwave absorption properties and morphology of manganese dioxide on catalytic oxidation of toluene under microwave irradiation

A large number of studies had shown that the morphology of the sample had a significant effect on the microwave absorption properties and catalytic activity of the sample. Manganese dioxide with different morphologies was synthesized by hydrothermal method through different precursors. The effects of sample morphology and microwave absorption properties on the catalytic activity of the sample in conventional thermal and microwave fields were studied. The results indicated that compared with the conventional thermal field, the catalytic activity of the samples in microwave field were obviously improved, and the activation energy of the reaction were decreased. Compared with the conventional thermal field, the conversion of toluene in microwave thermal field of MnO₂(Ac), MnO₂(S) and MnO₂(N) increased by 59%, 42% and 12%, and the mineralization rate increased by 36%,11% and 2%, respectively, when the catalytic temperature was 150 °C. Compared with the traditional thermal field, the activation energy of the sample MnO₂(Ac) in the microwave field was reduced by 88.3 KJ. A series of characterization results showed that the sample MnO₂(Ac) had good catalytic activity in the microwave field was due to: MnO₂(Ac) had proper microwave absorption properties, large amount of surface functional groups, large specific surface area and rich pore structure. The analysis results of electromagnetic parameters showed that: the reason that the sample MnO₂(Ac) had good microwave absorption performance was that the MnO₂(Ac) had proper impedance matching, high attenuation constant and Debye dipole relaxation effect.     

Microwave absorption properties of (1 − x)La0.85Ag0.15MnO3/x graphene (x = 0, 3, and 5 wt.%) composites

Composite of (1 − x)La_0.85Ag_0.15MnO₃/x graphene (x = 0, 3, and 5 wt.%) and epoxy resin with a ratio of 4:1 were prepared to investigate the influence of the addition of graphene in (1 − x)La_0.85Ag_0.15MnO₃/x graphene on real and imaginary parts of permittivity, permeability, as well as microwave reflection loss (RL), using a vector network analyzer in the 8–18 GHz of the frequency range. It is found that the value of RL is smaller at x = 3 wt.% (−20.74 dB at 14.85 GHz) and 5 wt.% (−14.81 at 16.50 GHz) compared to at x = 0 wt.% (−8.89 dB at 15.90 GHz). The result indicates that microwave absorption properties significantly improved as a result of the addition of graphene. It is suggested that the addition of graphene enhanced the dielectric loss–related mechanism such as interfacial polarization and conduction loss resulting in an improvement of microwave absorption performance for both x = 3 wt.% and x = 5 wt.% samples. It also shows that the observed enhanced microwave absorption properties may also be influenced by the resistivity of the sample as x = 3 wt.% sample exhibits enhanced microwave absorption properties and the lowest resistivity among the studied samples.     

Synthesis and magnetic properties of complex oxides La0.67Sr0.33MnO3 nanowire arrays

As a new approach of melt-injection-decomposition method, it has been successfully adopted for the synthesis of the complex oxides La_0.67Sr_0.33MnO₃ nanowire arrays. X-ray diffraction studies confirmed the formation of perovskite manganite phase of the sample. Transmission electron microscope and scanning electron microscope characterizations showed a large quantity of one-dimensional nanowires is obtained and the nanowires are continuous, concrete, oriented and rather uniform with an average diameter of 170 nm and length of several tens of micrometers. Magnetic measurements exhibited good ferromagnetic properties at the temperature of 10 K and 300 K respectively. The transition temperature of the complex oxides La_0.67Sr_0.33MnO₃ nanowire arrays is about 350 K, which will endow their great potential applications in magnetoresistance, spintronics or sensor fields at room temperature.     

Insights into the Reactivity of La1?xSrxMnO3 (x?=?0?÷?0.7) in High Temperature N2O Decomposition

Abstract  

In this paper a wide range of La_1−x Sr _x MnO₃ (x = 0–0.7) perovskites was synthesized by Pechini route, characterized by XRD (including high temperature measurements), XPS, differential dissolution phase analysis, TPR H₂, oxygen exchange and tested in N₂O decomposition at 900 °C. At low degree of Sr substitution for La (x ≤ 0.3), high catalytic activity was found for perovskites with hexagonal structure (x = 0.1–0.2) and can be related to fast oxygen mobility caused by the lattice disordering during polymorphic phase transition from the hexagonal to cubic structure. For multiphase samples (x > 0.3) increase of activity and oxygen mobility can be attributed to the formation of the layer-structured perovskite–LaSrMnO₄ on the surface.     

Synthesis of La1−xSrxMnO3 powders by polymerizable complex method: Evaluation of structural, morphological and electrical properties

Lanthanum strontium manganite (La_1−xSr_xMnO₃, LSM) powders were synthesized by polymerizable complex method, based on complexation of metal ions (MI) with citric acid (CA) and polyesterification between CA and ethylene glycol (EG). Firstly, the effect of the molar ratio of CA:MI (=1–3) was investigated on the synthesis of La_0.7Sr_0.3MnO₃ powders, which were characterized by thermal analysis (TGA/DTA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The results indicated that the molar ratio CA:MI = 3 is adequate for a good crystallization of pure perovskite phase after calcination, with nanometric crystallite sizes and porous microstructure. For the La_0.7Sr_0.3MnO₃ sample synthesized with CA:MI ratio of 3, it was investigated the effect of calcination temperature, showing that the perovskite structure is better crystallized at 900 °C, without secondary phase formation. Using this same CA:MI ratio and calcination temperature, powders with different Sr content (x = 0.2–0.4) were synthesized, with surface areas of 4–10 m² g⁻¹. These powders were sintered at 1100 °C to produce porous pellets. The porosity of the sintered pellets and the electrical conductivity, measured by two-probe technique, increased with increasing Sr content.