Magnetic properties of Nd0.5Pb0.5-xSrxMnO3 materials

The structure and magnetic properties of Nd0.5Pb0.5-xSrxMnO3 (0≤x≤0.4) manganites were systematically investigated. Significant changes in Curie temperature and metal-insulator (MI) transition temperature of the samples were observed. All samples exhibited a transition from paramagnetic semiconducting to ferromagnetic metallic state.Curie temperature Tc and the MI transition temperature Tp increased with increasing Sr content. We attributed these behaviours to the enhancing of both the double exchange mechanism and the Jahn-Teller electron-phonon coupling.     

Effect of cooling method on the electrochemical performance of 0.5Li2MnO3·0.5LiNi0.5Mn0.5O2 cathodes

0.5Li₂MnO₃·0.5LiNi_0.5Mn_0.5O₂ powders were synthesized by coprecipitation, and high temperature sintered with different cooled methods, such as cooled with furnace material, water material, and in liquid nitrogen (N-material). The effect of cooling methods on physical and electrochemical properties are discussed through the characterizations of X-ray diffraction (XRD), scanning electron microscopy, electrochemical impedance spectroscopy (EIS), and discharge, cyclic, and rate tests. XRD results show that all samples exhibit layered characteristics. The electrochemical performance results indicate that the N-material has the best electrochemical performance. The discharge capacity at 0.1 and 5 C are 279 and 99 mAhg^?1, respectively. The coulomb efficiency is highest, 78.4 %. The capacity retention after 50 cycles at 0.2 C is 97.1 %. EIS results show that the charge transfer resistance of N-materials is lowest, which is responsible for higher rate capacity.     

Thermal,Raman and dielectric study of 0.5K0.5Bi0.5TiO3–0.5PbTiO3 ceramics

The 0.5K_0.5Bi_0.5TiO₃–0.5PbTiO₃ ceramics were prepared by following a standard solid-state method. The Raman, thermal and dielectric properties of these ceramics were investigated. The X-ray measurements showed that samples have single perovskite-type structure with tetragonal symmetry. Dielectric study revealed that the dielectric behaviour of the investigated ceramics is rather of normal ferroelectrics with large thermal hysteresis. The transition temperature observed by means of differential scanning calorimetry measurements is in good agreement with that obtained from dielectric study.     

Magnetic properties of Nd0.5Pb0.5—xSrxMnO3 materials

The structure and magnetic properties of Nd_{0.5}Pb_{0.5-x}Sr_xMnO_3 (0≤x≤0.4) manganites were systematically investigated. Significant changes in Curie temperature and metal-insulator (MI) transition temperature of the samples were observed. All samples exhibited a transition from paramagnetic semiconducting to ferromagnetic metallic state. Curie temperature T_C and the MI transition temperature T_p increased with increasing Sr content. We attributed these behaviours to the enhancing of both the double exchange mechanism and the Jahn－Teller electron－phonon coupling.     

Structure evolution and microwave dielectric response of (Ca0.5+xSr0.5−x)[(Al0.5Nb0.5)0.5Ti0.5]O3 solid solutions

The phase assemblage, crystal structure evolution and microwave dielectric response of (Ca_0.5+xSr_0.5−x)[(Al_0.5Nb_0.5)_0.5Ti_0.5]O₃ ceramics (abbreviated as CSANT hereafter) are investigated. Single perovskite solid solution is formed in the CSANT ceramics in Sr-rich composition range of x < −0.05, however, Ca₄Ti₃O₁₀-type layered perovskite phase begins to segregate after x = −0.05. The CSANT perovskites crystallized in Fm3m cubic symmetry in the composition range of x ≤ −0.2, however, as the Ca²⁺ content in A-site increased, the oxygen octahedral began to be anti-phase tilted at x = −0.1 and the crystal structure transited to P2₁/n pseudo-orthorhombic space group thereafter. The microwave dielectric response of the CSANT ceramics is elaborately discussed in terms of their crystallographic structure and chemical composition. When sintered at 1500 °C for 4 h, a dielectric constant ɛ_r of 52.5, a Qf product of 28000 GHz and a τ_f of +25.4 ppm/°C microwave dielectric ceramic can be obtained in the CSANT ceramics at x = 0.3.     

Diffuse dielectric anomaly of （Na0.5K0.5Bi）0.5TiO3 crystal at high temperature

This paper investigates the dielectric properties of (Na_0.5K_0.5Bi)_0.5TiO₃ crystal at intermediate frequencies (1kHz \le f \le 1MHz) in the temperature range of 30--560℃. A pronounced high-temperature diffuse dielectric anomaly has been observed. This dielectric anomaly is shown to arise from a Debye-like dielectric dispersion that slows down following an Arrhenius law. The activation energy E_r obtained in the fitting process is about 0.69eV. It proposes that the dielectric peak measured at low frequency above 400℃ is not related to the phase transition but to a space-charge relaxation.     

μ+SR study of Ising spin-glass Fe0.5Mn0.5TiO3

A typical Ising spin-glass Fe_0.5Mn_0.5TiO₃ has been investigated by ⁺ spin relaxation measurements. It is found that the local magnetic fields at the ⁺ stopping sites appear at a temperature twice as high asT _SG. The directional distribution of the local magnetic fields is nearly isotropic, indicating the existence of the transverse spin components. It is clearly demonstrated that the spins fluctuate belowT _SG and even at 4 K. Taking into account the results obtained by other methods, the main part of the fluctuations is inferred to be due to the transverse spin components and the fluctuation limes at 4 K are driven into a range between 10^–5 and 10^–7 s.     

Grain-Size Effect on the Dielectric Properties of Bi0.5Na0.5TiO3

We prepared bismuth sodium titanate (Bi0.5Na0.5TiO3)ultrafine powders by the sol-gel method.The dielctric properties of the pressed pellets and fired ceramics with different grain sizes as a function of tempernature at various frequencies were studied.With decreasing grain size,the dielecric anomaly around 200℃ increases,while the dielectric thermal hysteresis decreases,All the samples with grain sizes larger than 100nm show dielectric peaks at temperature of about 350℃.The very little change in Tm observed down to the critical size indicates that Bi0.5Na0.5TiO3 is an order-disorder system above 200℃,In addition,the dielectric peak becomes lower with decreasing grain size and the ferroelectric critical size of Bi0.5Nan0.5TiO3 was eventually determined to be about 100nm according to the disappearance of dielectric peak.     

First Principles Study on Electronic Structure of PbFe0.5Nb0.5O3

The full potential linearized augmented plane wave (FLAPW) method is used to study the crystal structure and electronic structure properties of PbFeo.5 Nbo.5O3 (PFN). The optimized crystal structure, density of states, band structure and electron density distribution have been obtained to understand the ferroelectric behaviour of PFN.The analysis result of the density of states shows there is an obvious change of Nbd states in the paraelectric-to-ferroelectric phase transition. The polarization result shows that the contribution to ferroelectricity of Nb atoms is larger than that of Fe atoms. In ferroelectric phase there is a hybridization of Fed-Op and Nbd-Opin ferroelectric PFN. This is consistent with the result of the electronic band structure. This hybridization is responsible for the tendency to its ferroelectricity.     

Effect of oxygen content on the magnetic state of La0.5Ca0.5MnO3−γ perovskites

The magnetization and magnetoresistance are studied in La_0.5Ca_0.5MnO_3−γ as a function of oxygen content. It is found that as the oxygen content is decreased, this compound undergoes a sequence of transitions from an antiferromagnetic to a ferromagnetic state (γ⩾0.04), from the ferromagnetic to a spin-glass state (γ ⩾0.14), and from the spin glass to an inhomogeneous ferromagnetic state (γ⩾0.25). Strongly reduced samples (γ⩾0.25) show a large magnetoresistance despite the absence of Mn³⁺–Mn⁴⁺ pairs. It is suggested that the oxygen vacancies in the strongly reduced samples (γ⩾0.25) are long-range ordered. Pis’ma Zh. éksp. Teor. Fiz. 70, No. 9, 583–587 (10 November 1999) Published in English in the original Russian journal. Edited by Steve Torstveit.     

Microstructure and electrical properties of Bi0.5Na0.5TiO3–Bi0.5K0.5TiO3–LiNbO3 lead-free piezoelectric ceramics

Lead-free piezoelectric ceramics of (1?x?y)Bi_0.5Na_0.5TiO₃–xBi_0.5K_0.5TiO₃–yLiNbO₃ (BNT–BKT–LN-x/y) have been fabricated by a conventional solid-state reaction method, and their microstructure and electrical properties have been investigated. The results of X-ray diffraction (XRD) measurement show that K⁺, Li⁺ and Nb⁵⁺ diffuse into the Bi_0.5Na_0.5TiO₃ lattices to form a solid solution with a pure perovskite structure. The BKT and LN addition has no remarkable effect on the crystal structure. However, a significant change in grain size took place. Simultaneously, with increasing amount of LN, the temperature for a ferroelectric–antiferroelectric phase transition is clearly reduced. The temperature dependence of dielectric properties suggests that the ceramics have diffuse-type phase transition characteristics. The piezoelectric constant d₃₃ and the electromechanical coupling factor k_p of the ceramics attain maximum values of 195 pC/N and 0.336 at x=0.18 and y=0.01.     

Influence of Bi3+ doping on electronic transport properties of La0.5−xBixCa0.5MnO3 manganites

Electronic transport properties of La_0.5?xBi_xCa_0.5MnO₃ (x=0, 1/16, 1/8, 1/4, 3/8 and 1/2) compounds have been studied systematically to investigate their charge ordering (CO) behaviors. The results show that the CO temperature increases with the substitution of Bi³⁺ ion for La³⁺ ion, suggesting that the charge ordering is enhanced. This is attributed to the special role of the 6s² lone pair of Bi³⁺. It is found that for all the samples the adiabatic small polaronic conduction mechanism is responsible for the transport behavior above CO transition, whereas Mott's variable range hopping mechanism dominates below the CO transition. In addition, the electronic transport behavior of La_0.5?xBi_xCa_0.5MnO₃ compounds is high sensitive to an external magnetic field, which could raise fresh opportunities for application in magnetic sensors.     

Ferroelectric relaxor properties of (1 − x)K0.5Na0.5NbO3–xBa0.5Ca0.5TiO3 ceramics

The Ba_0.5Ca_0.5TiO₃ (BCT) composition dependent dielectric and structural properties of (1?x)K_0.5Na_0.5NbO₃–xBa_0.5Ca_0.5TiO₃ powders were investigated. Room temperature x-ray diffraction revealed the powder structure to transform from orthorhombic to cubic with increasing BCT composition. The frequency dependent dielectric constant measurements revealed a shift in the temperature of the maximum dielectric constant for at frequencies, suggesting that the system exhibits ferroelectric relaxor behavior. The system containing 15% BCT showed the closest calculated Curie–Weiss exponent to 2, which the exponent for a relaxor ferroelectric.     

Microstructure and magnetic characteristics of nanocrystalline Ni0.5Zn0.5 ferrite synthesized by a spraying-coprecipitation method

Nanocrystalline Ni0.5Zn0.5 ferrite with average grain sizes ranging from 10 to 100 nm is prepared by using a spraying-coprecipitation method. The results indicate that the nanocrystalline Ni0.5Zn0.5 ferrite is ferromagnetic without the superparamagnetic phenomenon observed at room temperature. Specific saturation magnetization of nanocrystalline Nio.sZno.5 ferrite increases from 40.2 to 75.6 emu/g as grain size increases from 11 to 94nm. Coercivity of nanocrystalline Ni0.5Zn0.5 ferrite increases monotonically when d 〈 62 nm.The relationship between the coercivity and the mean grain size is well fitted into a relation Hc - d^3. A theoretically evaluated value of the critical grain size is 141nm larger than the experimental value 62nm for nanocrystalline Ni0.5Zn0.5 ferrite. The magnetic behaviour of nanocrystalline Ni0.5Zn0.5 ferrite may be explained by using the random anisotropy theory.     

Dielectric and piezoelectric properties of Li-substituted lead-free (Bi0.5Na0.5)TiO3–(Bi0.5K0.5)TiO3–BaTiO3 ceramics

Lead-free 0.79(Bi_0.5Na_0.5)TiO₃–0.14[Bi_0.5(K_0.5−xLi_x)]TiO₃–0.07BaTiO₃ (BNBK79 + xLi, x = 0.0, 0.1, 0.2, 0.25, 0.3, and 0.4) ceramics were prepared by conventional solid state reaction process. The crystalline structures and surface morphologies are investigated by X-ray diffraction method and scanning electron microscopy. Dielectric and piezoelectric properties were measured. With increasing of lithium substitution, the Curie temperatures of BNBK79 + xLi ceramics increase, but the maximum value of the dielectric constant decreases. And a relatively large remnant polarization of 17.6 μC/cm² and 157 pC/N of d₃₃ has been obtained when x = 0.3.     

Effects of A-site disorder on magnetic,electrical and thermal properties of La0.5−xLnxCa0.5−ySryMnO3manganites

The magnetic, electrical and thermal properties in the La_0.5?xLn_xCa_0.5?ySr_yMnO₃ (Ln=Pr, Nd, Sm) bulk system were investigated. Detailed dc magnetization and linear ac susceptibility measurements reveal that the samples first undergo phase transition from paramagnetic to ferromagnetic phase and then to an antiferromagnetic phase upon further cooling. It is found that both the Curie and Neel temperatures decrease systematically with increasing A-site disorder in these manganites. The electrical resistivity exhibits semiconducting behavior throughout the temperature range investigated and the electronic conduction mechanism can be conveniently described within the framework of the variable range hopping model above T=150 K. The Seebeck coefficient (S) in the magnetically ordered regime infers that the complicated temperature dependence of S is an indication of electron–magnon scattering. Specific heat measurements depict a broadened hump in the vicinity of T_C, indicating the existence of magnetic ordering and magnetic inhomogeneity in the samples. The temperature dependence of thermal conductivity, κ(T), reveals a positive dκ/dT in the paramagnetic region, which may be related to the local anharmonic lattice distortions associated with small polarons.     

Suppression of charge ordering and thermal hysteresis of electronic transport and magnetisation in La0.5Ca0.5Mn1−xNixO3

A series of polycrystalline La_0.5Ca_0.5Mn_1?xNi_xO₃ (x = 0.00, 0.025, 0.050, 0.075, 0.100 and 0.125) was synthesised using solid state reaction. Measurements in a cooling and warming cycle between 300 and 80 K were carried out to study the Ni-doping effects on the electrical resistivity, thermopower and magnetisation of single-phase La_0.5Ca_0.5Mn_1?xNi_xO₃. Partial substitution of Ni for Mn leads to the suppression of charge ordering state, the evidence of which is shown by the dramatic decrease in electrical resistivity and thermal hysteresis width in electrical resistivity, thermopower and magnetisation. However, the magnitude of both electrical resistivity and thermopower increases with increasing Ni content. This can be attributed to an increase in the Mn⁴⁺ concentration, which favours the antiferromagnetic state and leads to a gradual disappearance of ferromagnetic double exchange interaction. Besides, the metal–nonmetal transition temperature decreases with increasing Ni content until x = 0.075, which might arise from increased electron–phonon coupling due to less ordered spins at temperatures above ferromagnetic transition. For samples with x greater than 0.075, no metal–nonmetal transition is observed due to the suppression of double exchange mechanism.     

Neutron diffraction studies of the magnetic properties of Pr0.5Sr0.5Co1 ? x Mn x O3 solid solutions

The crystal structure and magnetic properties of a system of Pr_0.5Sr_0.5Co_{1 ? x} Mn _x O₃ solid solutions were studied by neutron diffraction and magnetization measurements. It is shown that, at a low manganese concentration, the structure can be described by the I/2a monoclinic space group; with increasing substitution level x the structure becomes orthorhombic. For x > 0.9 the crystal structure is tetragonal at high temperatures and the symmetry is lowered to orthorhombic with lowering the temperature. The substitution of cobalt for manganese leads to the destruction of long-range ferromagnetic order near x ?? 0.25. A transition from the high-temperature ferromagnetic phase to the A-type low-temperature antiferromagnetic phase is observed at x ?? 0.93 in the temperature range 110?C160 K.