Magnetic phase transitions and magnetoresistance in the La0.7Ba0.3(Mn1−xMex)O3 (Me=Fe,Al) single crystals and La0.7Sr0.3(Mn1−xMex)O3 (Me=Fe,Cr, Al) ceramics

The single crystals of La_0.7Ba_0.3(Mn_1−xFe_x)O₃ (x⩽0.28) and La_0.7Ba_0.3(Mn_1−xAl_x)O₃ (x⩽0.15) compositions were grown using flux method and characterized by X-ray, electrical and magnetization measurements. The Fe-doping above x=0.2 destroys a long range ferromagnetic order thus leading to a spin glass state. It is found that insulating spin glasses exhibit a large magnetoresistance in the paramagnetic region which is comparable to that for ferromagnetic crystals showing metal–insulator transition close to T_C. The magnetic behavior of La_0.7Ba_0.3(Mn_1−xMe_x)O₃ (Me=Fe, Cr, Al) ceramics is in agreement with superexchange magnetic interactions via oxygen.     

La0.7Ca0.3Mn1-xCrxO3的激光超声研究

运用激光超声的方法测定了五种不同掺杂的巨磁锰氧化物La0.7Ca0.3Mn1-xCrxO3(0.01≤x≤0.60)室温(300 K)下的超声纵波声速.结合热导率的数据,对声速随掺杂浓度的变化原因进行了深入的分析.得到在顺磁绝缘态Cr3 离子的掺入造成了晶格局部涨落的变化,低掺杂使得晶格局部涨落增强,声子U散射弛豫时间减小.     

Dielectric and piezoelectric properties of (1−x)Ba0.7Sr0.3TiO3−xBa0.7Ca0.3TiO3 perovskites

Dielectric and piezoelectric properties of (1?x)Ba_0.7Sr_0.3TiO₃?xBa_0.7Ca_0.3TiO₃ (BST?xBCT) (x=0.2–0.9) perovskite ceramics have been investigated. BCT has fully incorporated into BST lattice, forming a complete perovskite solid solution, whose lattice constant χ decreases almost linearly with increase in x from 0.2 to 0.4, while showing an anomalous expansion at 0.4<x≤0.6. This, together with the deviation of tetragonal–orthorhombic phase transition temperature (T_O–T) from the linear relation T_O–T (K)=?103.7x+239.3 at x=0.5, suggests that a small amount of Ca²⁺ has substituted for Ti⁴⁺. Curie temperature T_C increases linearly with increase in x from 0.2 to 0.9, which is mainly contributed to the increase of the Ba/Sr ratio. The calculated degree of relaxation (γ) is in the range of 1.41–1.53, indicating that the BST–xBCT ceramics are ferroelectric materials with diffuse phase transition. Strain and piezoelectric constant (d₃₃) decrease with increasing x, whereas planar electromechanical coefficient (k_p) reaches a maximum (17.0%) at x=0.6.     

Spin Glass Behaviour and Spin-Dependent Scattering in La0.7Ca0.3Mn0.9Cr0.1O3 Perovskites

The magnetic, electrical and thermal transport properties of the perovskite La0.7Ca0.3Mn0.9 Cr0.1O3 have been investigated by measuring dc magnetization, ac susceptibility, the magnetoresistance and thermal conductivity in the temperature range of 5-300 K. The spin glass behaviour with a spin freezing temperature of 70 K has been well confirmed for this compound, which demonstrates the coexistence and competition between ferromagnetic and antiferromagnetic clusters by the introduction of Cr. Colossal magnetoresistance has been observed over the temperature range investigated. The introduction of Cr causes the ““double-bump““ feature in electrical resistivity ρ(T). Anomalies on the susceptibility and the thermal conductivity associated with the double-bumps in ρ(T)are observed simultaneously. The imaginary part of ac susceptibility shows a sharp peak at the temperature of insulating-metallic transition where the first resistivity bump was observed, but it is a deep-set valley near the temperature where the second bump in ρ(T) emerges. The thermal conductivity shows an increase below the temperature of the insulating-metallic transition, but the phonon scattering is enhanced accompanying the appearance of the second peak of double-bumps in ρ(T). We relate those observed in magnetic and transport properties of La0.7Ca0.3Mn0.9Cr0.1O3 to the spin-dependent scattering. The results reveal that the spin-phonon interaction may be of more significance than the electron (charge)-phonon interaction in the mixed perovskite system.     

La0.3Ca0.7Mn1-xWxO3体系电荷有序的建立与融化

用标准的固相反应法制备了La0.3Ca0.7Mn1-xWxO3(0.00≤X≤0.15)多晶样品.通过对样品磁化强度-温度(M-T)曲线、磁化强度-磁场强度(MH)曲线及ESR谱的测量,研究了Mn位W掺杂对La0.3Ca0.7Mn1-xWxO3体系的磁相变的影响.结果表明,随着W掺杂量的增加,体系磁相变发生了复杂的变化过程.当掺杂量为0.00≤X≤0.08时,体系存在电荷有序(CO)相,反铁磁(AFM)/C0态共存于相变温度以下,电荷有序温度(Tco)随着W掺杂量的增加而增加.x≥0.12时,体系电荷有序态逐渐减弱并融化,在极低温度下存在顺磁-铁磁(PM-FM)相变.     

Magnetic and electrical properties of weakly doped manganese-deficient La1 − x Ca x Mn1 − z O3 manganites

Samples of La_{1 ? x} Ca _x Mn_{1 ? z} O_{3 + δ} (x = 0.05?0.15) with deficient manganese and excess oxygen δ do not pass into a metallic state and have low spin ordering temperatures T _C at acceptor Mn⁴⁺ concentrations near the percolation threshold. These results are explained by carrier localization in clusters near cation vacancies. A break in the carrier transport chain Mn-O-Mn in the form of absent manganese favors cluster formation and decreases the double exchange energy and T _C of the samples. Closeness to the percolation threshold results in strong (more than four orders of magnitude) changes in the electrical resistivity in a magnetic field. The changes in the cluster sizes with the temperature and the magnetic field that are determined from the magnetotransport properties are satisfactorily described in the model of phase separation into small-radius metallic droplets in a dielectric paramagnetic and an antiferromagnetic matrices.     

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.     

Ionic and electronic conductivity in CaTi1−xFexO3−δ (x=0.1–0.3)

Electrical conductivity measurements on CaTi_1?xFe_xO_3?δ (x=0.1, 0.2, 0.3) were performed on polycrystalline pressed and sintered tablets using the van der Pauw four point method in controlled atmospheres. The results were interpreted to reflect n-type, ionic and p-type conductivity at different oxygen partial pressures. An increasing iron content increases the number of oxygen vacancies and increases the ionic conductivity at high temperatures, but also increases the tendency of ordering, which suppresses the ionic conductivity at more moderate temperatures. These findings are in accordance with the phase diagram of the system CaTiO₃-CaFeO_2.5 based on X-ray and Mössbauer studies.     

Ultrafast optical probes of dynamic behavior in La0.7Sr0.3MnO3/YBa2Cu3O7 − δ/La0.7Sr0.3MnO3 heterostructure

Ultrafast pump-optical probe spectroscopy was used to analyze carriers dynamics behavior in La_0.7Sr_0.3MnO₃/YBa₂Cu₃O_{7 ? δ}/La_0.7Sr_0.3MnO₃ heterostructure. Our results show the pump signal ΔR/R for higher laser power (such as 21 and 41 mW), below T _c , first goes positive, then crosses zero and goes negative, before relaxing back to equilibrium over a time scale of a few ten picoseconds. We extract the characteristic relaxation time of the different process by fitting the data at these powers with a three-exponential decay. For higher laser power, the long characteristic relaxation time are obtained, which implies the competition between FM order and SC order in the La_0.7Sr_0.3MnO₃/YBa₂Cu₃O_{7 ? δ}/La_0.7Sr_0.3MnO₃ heterostructure.     

Ultrafast Photoelectric Effects in Heterojunctions of La0.7Sr0.3MnO3 and Si

Ultrafast photoelectric effects have been observed in p-n heterojunctions of La0.7Sr0.3MnO3(LSMO)/Si and LSMO/SrTiO3_/Si for the first time. The rise time was about 1 ns and the full width at half maximum was about 2ns for the photovoltaic pulse when the heterojunction was irradiated by a laser of -25 ps pulse duration and 1064 nm wavelength. The photovoltaic sensitivity was as large as 435 mV//mJ for a 1064 nm laser pulse. No such pulse was observed with irradiation from a pulsed 10.6 μm CO2 laser.     

Enhancement in multiferroic properties of Bi0.7−xLaxDy0.3FeO3 system with removal of La

La doping at Bi Site in multiferroic BiFeO₃ (BFO) is known to stabilize the ferroelectric perovskite phase and reduce the leakage current. It has been observed that in Dy modified BFO sample, La is not required for the said reason. In fact, the removal of La from Dy modified BFO system leads to the reduction in leakage current. Moreover, the magnetic properties are enhanced by order of magnitude in the absence of La in the system. Remarkably, a similar trend in properties has been also observed in thin films grown on Pt/TiO₂/SiO₂/Si substrate by using the pulsed laser deposition technique. This significant variation in the properties after removal of La from the system could be attributed to the change in lattice parameters, bond lengths and Fe–O–Fe bond angle as determined by powder x-ray and neutron diffraction study.     

In-plane and out-of-plane anisotropic magnetoresistances in La1 − x Pb x MnO3 thin films

The temperature and field dependences of in-plane (IP) and out-of-plane (OP) anisotropic magnetoresistances (AMRs) have been measured in La_{1 ? x} Pb _x MnO₃ (LPMO) thin films having different microstructures, namely the single-crystal (SC), nanocrystalline (NC) and polycrystalline (PC) microstructures. The OP AMR, irrespective of the microstructure, is found to be considerably larger than the IP AMR. The magnetization data show that the larger OP AMR arises because magnetization is favoured in the film plane owing to strain anisotropy. In addition, the temperature and field dependences of both IP and OP AMRs are governed by the crystallinity of the films, indicating that the AMRs are strongly influenced by the magnetization process.     

La0.7-xGdxSr0.3MnO3体系中的相分离

采用固相反应法制备了样品La0.7-xGdxSr0.3MnO3(x=0.00,0.20,0.30,0.40,0.50).通过测量样品的M～T曲线,ESR曲线,研究了La0.7-xGdxSrO0.3MnO3,体系中的相分离现象及相分离与CMR之间关系.结果表明:当x=0.30,0.40时,在PM-FM相变区产生相分离,并且磁电阻MR得到增强.研究结果表明:La0.7-xGdx Sr0.3MnO3中的相分离与Gd在A位的占位情况紧密相关,磁电阻MR的增强是在外磁场作用下,铁磁区扩大顺磁区减小引起的.     

Structural and magnetic characterisation of the perovskite oxides La0.7Ca0.3−x Na x MnO3

X-ray powder diffraction (XRD) and magnetic measurements were performed in order to investigate the effect of Na⁺ ion substitution for Ca²⁺ ions on the crystallographic structure, the character of magnetic ordering, and the effect of transition temperature in La_0.7Ca_0.3−x Na _x MnO₃ manganites series (0 ⩽ × ⩽ 0.2). All samples crystallise in an orthorhombic structure with the Pnma space group. We have found a strong dependence of structural and magnetic properties on the cation-size disorder parameter σ ². The temperature dependence of magnetization of all samples obeys the Bloch T ^3/2 law. The values of the spin wave constant at low temperature B increase with the increase of x and the Curie temperature decreases. It is concluded that the substitution of Ca by Na⁺ ions causes a decrease in total exchange integral Aof the samples.      

Magnetic ordering and magnetoresistive effect in La1−x Srx(Mn1−y Mey)O3 perovskites (Me = Nb, Mg)

Perovskites of composition La_1?x Sr_x(Mn_1?x/2Nb _x/2)O₃ and La_0.49Sr_0.51(Mn_1?y Nb_y)O₃ have been synthesized and investigated. The substitution of nonmagnetic niobium ions for manganese was shown to lead to a transition from the metallic into the insulating state due to a decrease in the number of dissimilar (different-valence) manganese atoms in the lattice. In spite of the high resistivity, the niobium-containing perovskites exhibit a large magnetoresistive effect and ferromagnetic ordering. Small additions of Nb⁵⁺ to La_0.49Sr_0.51MnO₃ stimulate the transition from the antiferromagnetic into the ferromagnetic state, whereas the substitution of Mg²⁺ for Mn stabilizes the antiferromagnetic state. It is supposed that the ferromagnetism in the insulating perovskites at hand is due to the positive superexchange of the Mn³⁺-O-Mn³⁺ type, and the magnetoresistive effect owes to the intergranular transfer of spin-polarized charge carriers and the suppression of magnetic nonuniformities by an applied magnetic field near T _C.     

Deoxygenation Enhanced Double-Resistivity-Peak Properties in Polycrystalline La0.7Ca0.3Mn0.92Cr0.08O3-δ

Influences of deoxygenation on the resistivity and the magnetic properties of La0.7Ca0.3Mn0.92Cr0.08O3-δ(M =Al, Cr) are compared to understand the peculiar doping effect of chromium in the ferromagnetic manganites. It is found that the double resistivity bumps exhibited by the Cr-doped compounds can be tuned by the oxygen content. We have related the double-bump feature with the well-known inefficiency of Cr in lowering Tc, and interpreted both the features consistently in terms of large-scale phase separation. It is suggested that the largescale phase separation is a general characteristic of Cr-doped manganites, and many unusual phenomena exhibited by Cr doping are directly related to the large-scale phase separation.