Hall resistivity in ferromagnetic manganese-oxide compounds

The transport properties of manganese-oxides are studied using the spin correlation fluctuation scattering mechanism. It is shown that the Hall resistivity in a small magnetic field exhibits a maximum near the Curie point, and a strong field shifts the peak position to high temperature and suppresses the peak value; the dependence of the Hall resistivity on the magnetic field above T_c and below T_c is different. These results agree with the experimental curves qualitatively, but disagree quantitatively, which indicates that the spin correlation fluctuation scattering might not be the dominant mechanism of the colossal magnetoresistance. The double polaron mechanism due to strong electron-phonon and electron-spin coupling is proposed to be responsible for the colossal magnetoresistance in manganese-oxides.     

Colossal Magnetoresistance of Layered Manganite La<Subscript>1.2</Subscript>Sr<Subscript>1.8</Subscript>Mn<Subscript>2</Subscript>O<Subscript>7</Subscript> and Its Description by a “Spin–Polaron” Conduction Mechanism

The resistance of a La_1.2Sr_1.8Mn_2(1–z)O₇ single crystal has been studied in magnetic fields from 0 to 90 kOe. The magnetoresistance at temperature T = 75 K, near which a colossal magnetoresistance maximum is observed, has been successfully described in terms of the “spin–polaron” electric conduction mechanism. This value of the colossal magnetoresistance is due to a three-fold increase in the polaron size. The method of separating contributions of various conduction mechanisms to the magnetoresistance developed for materials with activation type of conduction is generalized to compounds in which a metal–insulator transition is observed. It is found that, at a temperature of 75 K, the contribution of the “orientation” mechanism is maximum (≈20%) in a magnetic field of 5 kOe and almost disappears in fields higher than 50 kOe.     

Magnetoresistance of lanthanum manganites with activation-type conductivity

The temperature dependence of the resistivity and magnetic moment of La_0.85Ba_0.15MnO₃ and La_0.85Sr_0.15MnO₃ manganite single crystals in magnetic fields up to 90 kOe is investigated. Analysis of the experimental results shows that the magnetoresistance of lanthanum manganites far from the Curie temperature T _C can be described quantitatively by the s-d model normally used for ferromagnets and taking into account only the exchange interaction between the spins of charge carriers and magnetic moments. These data also show that the features of lanthanum manganites responsible for colossal magnetoresistance (CMR) are manifested in a narrow temperature interval δT ≈ 20 K near T _C. Our results suggest a CMR mechanism analogous to the mechanism of giant magnetoresistance (GMR) observed in Fe/Cr-type multilayers with nanometer layer thickness. The nanostratification observed in lanthanum manganites and required for GMR can be described taking into account the spread in T _C in the CMR range δT.     

La0.7Sr0.3MnO3 film prepared by dc sputtering on silicon substrate: Effect of working pressure

La_0.7Sr_0.3MnO₃ films were prepared by dc sputtering on Si (100) substrate at different working pressure. The possibility of controlling the magnetic and transport properties of colossal magnetoresistance film is investigated, which has attracted great research interest for practical application. The as-grown film shows different magnetic, transport and magnetoresistance change at different working pressure at room temperature, which is quite attractive from technological point of view. Maximum magnetoresistance (MR) of ?5.56%, Curie temperature (T_c) of 325 K and metal insulator transition temperature (T_MI) of 278 K was achieved at room temperature.     

Two-phase paramagnetic-ferromagnetic state of La<Subscript>0.7</Subscript>Pb<Subscript>0.3</Subscript>MnO<Subscript>3</Subscript> single-crystal lanthanum manganite

Two phases, paramagnetic and ferromagnetic, were shown by the magnetic resonance method to coexist below the temperature T _C in La_0.7Pb_0.3MnO₃ single crystals exhibiting colossal magnetoresistance. The magnetic resonance spectra were studied in the frequency range 10–78 GHz. The specific features in the behavior of the spectral parameters were observed to be the strongest at the temperatures corresponding to the maximum magnetoresistance in the crystals. The concentration ratios of the paramagnetic and ferromagnetic phases in the samples were found to be sensitive to variations in temperature and external magnetic field. This behavior suggests realization of the electronic phase separation mechanism in the system under study.     

La1－xPrxMnO3(x=0.1，0.2)薄膜庞磁电阻性质的研究

一种新的庞磁电阻氧化物薄膜La_1-xPr_xMnO₃(x=0.1，0 .2)薄膜用脉冲激光沉积(PLD)方法生长在(100)SrTiO₃单晶基底上.XRD结果显示 薄膜具有很好的外延单晶取向.电输运和磁性质的研究表明薄膜具有显著的庞磁电阻效应(CM R)效应，其中磁电阻比率达95％(在5T的磁场下).X射线光电子能谱(XPS)的结果表明薄膜体 系中Pr离子的价态为+4价，因此该薄膜很可能是电子掺杂的庞磁电阻体系. 关键词： 脉冲激光沉积 1-xPr_xMnO₃')" href="#">La_1-xPr_xMnO₃ 电子 掺杂 庞磁电阻     

Effect of inhomogeneity on magnetic, magnetocaloric, and magnetotransport properties of La0.6Pr0.1Ca0.3MnO3 single crystal

The effect of magnetic inhomogeneity on magnetic, magnetocaloric, and transport properties of the colossal magnetoresistance manganites with first order ferromagnetic-to-paramagnetic phase transition is studied. The experiments were performed on the single-crystalline samples of La_0.6Pr_0.1Ca_0.3MnO₃. The inhomogeneity is described by the Curie temperature distribution function, which is found from the magnetization data. The temperature dependence of the magnetic field induced change in the entropy is shown to be determined by the distribution function and the shift of the transition temperature in a magnetic field. Similarly, magnetoresistance in the transition region is determined by the resistivity at H=0 and the shift of the transition temperature. The maximum entropy change as well as maximum magnetoresistance can be achieved in the magnetic field of order δT_C/B_M where δT_C is the transition width and B_M is the rate of change of the Curie temperature with magnetic field.Our approach to analysis of the effects of inhomogeneity is general and therefore can be used for all compounds with the first order magnetic phase transition.     

Effect of oxygen non-stoichiometry on magnetic and electrical transport properties of La0.67Sr0.33MnO3

The effect of oxygen deficiency and oxygen excess on the magnetic and electrical transport properties of La_0.67Sr_0.33MnO₃ has been investigated. The thermal and isothermal magnetization measurement results show that the Curie temperature and saturation magnetization of oxygen deficient sample (defined as A) are higher than those oxygen excess sample (defined as B). The electrical resistivity of A is lower than that of B in studied temperature range. The magnetoresistance (MR) of B is larger than that of A in the temperature range from 280 to 360 K, which agrees with the magnetic field needed full spin polarization at room temperature. The colossal MR (CMR) around transition temperature from ferromagnetic metal to paramagnetic insulator (T_MI) for A is larger than that for B, which arises from assistance of stronger lattice deformation for A.     

Anomalous influence of an external magnetic field on spin fluctuations in magnetic semiconductors with strong p-d hybridization and the colossal magnetoresistance effect

The colossal magnetoresistance effect in magnetic semiconductors based on lanthanum manganites has been investigated in terms of the model allowing for the effects of p-d hybridization and electronelectron Coulomb correlations. The influence of an external magnetic field on spin fluctuations has been considered under the conditions where the chemical potential is in a narrow heavy-fermion band formed in the hybridization gap. It has been shown that, in the vicinity of the Curie point T _C, the strong spin anharmonicity leads to an anomalously strong suppression of spin fluctuations by the external magnetic field, a phenomenon contributing significantly to the formation of colossal negative magnetoresistance.     

The giant volume magnetostriction and colossal magnetoresistance in Eu<Subscript>0.55</Subscript>Sr<Subscript>0.45</Subscript>MnO<Subscript>3</Subscript> manganite

A doped manganite with the composition Eu_0.55Sr_0.45MnO₃ exhibits giant negative magnetostriction and colossal negative magnetoresistance at temperatures in the vicinity of the magnetic phase transformation (T～41 K). In the temperature interval 4.2 K≤T ≤40 K, the isotherms of magnetization, volume magnetostriction, and resistivity exhibit jumps at the critical field strength H_c1, which decreases with increasing temperature. At 70 K ≤T ≤120 K, the jumps on the isotherms are retained, but the shapes of these curves change and the H_c1 value increases with the temperature. At H<H_c1, the magnetoresistance is positive and exhibits a maximum at 41 K; at H>H_c1, the magnetoresistance becomes negative, passes through a minimum near 41 K and then reaches a colossal value. The observed behavior is explained by the existence of three phases in Eu_0.55Sr_0.45MnO₃, including a ferromagnetic (in which the charge carriers concentrate due to a gain in the s-d exchange energy) and two antiferromagnetic phases (of the A and CE types). The volumes of these phases at low temperatures are evaluated. It is shown that the colossal magnetoresistance and the giant volume magnetostriction are related to the ferromagnetic phase formed as a result of the magnetic-field-induced transition of the CE-type antiferromagnetic phase to the ferromagnetic state.     

Effect of strontium deficiency on the transport and magnetic properties of Pr0.7Sr0.3MnO3

Ceramic samples of Pr_0.7Sr_0.3−x□_xMnO₃ with x⩽0.2 have been investigated by various techniques including ⁵⁵Mn nuclear magnetic resonance, SQUID magnetometry, resistivity and magnetoresistance measurements. On increasing x, the samples remain ferromagnetic at a low temperature with a decreasing Curie temperature, but a metal–insulator transition is observed. Besides, a positive magnetoresistance (MR) at very low temperatures with respect to a negative colossal MR at high temperatures is observed in the Pr_0.7Sr_0.2□_0.1MnO₃ sample.     

Electrical transport and magnetic properties of perovskite-type electron-doped La–Pr–Mn–O epitaxial films

La_1−xPr_xMnO₃ (LPrMO) thin films have been epitaxially grown on (1 0 0)SrTiO₃ single-crystal substrates by pulsed-laser deposition. The films have a perovskite structure and give rise to the colossal magnetoresistance effect with the maximum magnetoresistance ratio of 10³% (at 240 K and 5 T). The electrical transport and magnetic properties have been investigated for the La_0.8Pr_0.2MnO₃ film with thickness 3000 Å. The results indicate that the films have quite a distinctive magnetotransport behavior compared to the bulk. The analysis of X-ray photoemission spectroscopy suggests that the valence state of Pr is 4+ in LPrMO film. Therefore, the epitaxial film is most likely an electron-doped colossal magnetoresistance system.     

Nature of the low-temperature colossal magnetoresistance of La0.35Nd0.35Sr0.3MnO3 epitaxial films

The colossal negative magnetoresistance (approximately 12%) in a field of 8.4 kOe over a wide range of temperatures below the Curie point T _C ≈240 K in a single-crystal La_0.35Nd_0.35Sr_0.3MnO₃ film on a single-crystal (001)ZrO₂(Y₂O₃) wafer substrate is discussed. Isotherms of the magnetoresistance of this film reveal that its absolute value increases with the field, abruptly in the technical magnetization range and almost linearly in stronger fields. For three single-crystal films of the same composition on (001)LaAlO₃, (001)SrTiO₃, and (001)MgO substrates, colossal magnetoresistance only occurred near T _C ≈240 K and at T<T _C it increased weakly, almost linearly, with the field. In the film on a ZrO₂(Y₂O₃) substrate the electrical resistivity was almost 1.5 orders of magnitude higher than that in the other three films. It is shown that this increase is attributable to the electrical resistance of the interfaces between microregions having four types of crystallographic orientations, while the magnetoresistance in the region before technical saturation of the magnetization is attributable to tunneling of polarized carriers across these interfaces which coincide with the domain walls (in the other three films there is one type of crystallographic orientation). The reduced magnetic moment observed for all four samples, being only 46% of the pure spin value, can be attributed to the existence of magnetically disordered microregions which originate from the large thickness of the domain walls which is greater than the size of the crystallographic microregions and is of the same order as the film thickness. The colossal magnetoresistance near T _C and the low-temperature magnetoresistance in fields exceeding the technical saturation level can be attributed to the existence of strong s-d exchange which is responsible for a steep drop in the carrier mobility (holes) and their partial localization at levels near the top of the valence band. Under the action of the magnetic field the carrier mobility increases and they become delocalized from these levels.     

Giant volume magnetostriction and colossal magnetoresistance in La0.7Ba0.3MnO3 at room temperature

In single-crystal La_0.7Ba_0.3MnO₃, giant volume magnetostriction was observed for the first time to reach 2.54 × 10^?4 at room temperature and a still larger level of 4 × 10^?4 at the Curie point T _C = 310 K in a magnetic field of 8.2 kOe. At the same temperatures and magnetic field, this effect is complemented by a colossal magnetoresistance of 15.2 and 22.7%, respectively. The volume magnetostriction ω and magnetoresistance Δρ/ρ follow similar patterns in the proximity of T _C; namely, ω and Δρ/ρ are negative, maxima are observed in the |ω|(T) and |Δρ/ρ|(T) curves, and the ω and Δρ/ρ isotherms do not saturate in the highest fields applied. These phenomena are assigned to the fact that, in the above composition, there exists a two-phase magnetic (ferromagnetic-antiferromagnetic) state induced by strong s–d exchange.     

Study of structural, transport and magneto-resistive properties of La0.7Ca0.3−xCexMnO3 (0≤x≤0.2)

We have synthesized a series of La_0.7(Ca_0.3−xCe_x)MnO₃ (0≤x≤0.2) by standard solid-state reaction method. X-ray diffraction (XRD) measurement was carried out for structural studies and Rietveld refinement was done for structural analysis. The transport properties were studied using four probe technique. The temperature dependence of the resistivity was measured in the temperature range of 20 K to room temperature. It is found that all samples show a systematic variation in metal to insulator transition at transition temperature (T_P) and resistivity (ρ) with the relative concentration of hole and electron doping in the system. The samples showed varying amounts of colossal magnetoresistance depending upon temperature and applied magnetic field. The magnetoresistance values as high as 72% were observed in x=0 sample.     

Magnetorefractive effect in La<Subscript>0.7</Subscript>Ca<Subscript>0.3</Subscript>MnO<Subscript>3</Subscript> in the infrared spectral range

The reflection and magnetic reflection spectra, magnetic resistance, electrical properties, and equatorial Kerr effect in La_0.7Ca_0.3MnO₃ crystals have been complexly investigated. The measurements have been performed in wide temperature and spectral ranges in magnetic fields up to 3.5 kOe. It has been found that magnetic reflection is a high-frequency response in the infrared spectral range to the colossal magnetore-sistance near the Curie temperature. Correlation between the field and temperature dependences of the magnetic reflection and colossal magnetoresistance has been revealed. The previously developed theory of the magnetorefractive effect for metallic systems makes it possible to explain the experimental data at the qualitative level. Both demerits of the theory of the magnetorefractive effect in application to the magnets and possible additional mechanisms responsible for the magnetic reflection are discussed.     

Effect of disorder and isotope on the properties of a two orbital double exchange system

A two-site single electron double exchange model incorporating orbital degeneracy, superexchange and electron-phonon (e-ph) interaction is studied using exact diagonalization method. The core spins are treated quantum mechanically. We study the ground state phase diagram as well as the magnetic susceptibility and the kinetic energy of the system as a function of temperature. Effect of difference in site energies, which mimics the role of site-diagonal disorder, is investigated. The susceptibility shows a peak at a characteristic temperature which we have referred to as T₀. The variation of T₀ with e-ph coupling and that of the isotope-shift exponent (α) with T₀ are obtained. We also investigate the field-induced change in the kinetic energy, which is related to the colossal magnetoresistance (CMR) of the system, and find that the disorder enhances the CMR even for the two-site system.     

Relation between giant volume magnetostriction and colossal magnetoresistance near the Curie temperature of Sm0.55Sr0.45MnO3

The magnetic, transport, and elastic properties of Sm_0.55Sr_0.45MnO₃ have been established to be interrelated. At the Curie point, one observes a large volume compression ΔV/V≈0.1%, a sharp minimum in the temperature dependence of negative volume magnetostriction ω(T), and a maximum in the temperature dependence of the electrical resistivity. Giant negative volume magnetostriction ω=?5×10^?4 has been found in a magnetic field H=0.9 T, which is accompanied by a colossal negative magnetoresistance of 44% in the same field. The results obtained are discussed in terms of a model of electronic phase separation.     

Oxygenation-induced two peaks in the self-doped La0.9MnO3+δ compounds

A series of self-doped La_0.9MnO_3+δ compounds have been fabricated by the solid-state reaction method with different post-annealing and oxygenation processes. The temperature dependence of resistivity measured at several magnetic fields indicated that all of these samples have an insulator–metal transition with a large negative colossal magnetoresistance (CMR) ratio. The resistivity, maximum CMR ratio and peak position are dominated by the oxygen content. As the oxygen content increases, the resistivity decreases, the peak position shifts to higher temperature and the maximum CMR ratio increases, respectively; meanwhile the peak number in the R–T curve is changed from 1 to 2, then from 2 to 1. The temperature dependencies of magnetization and specific heat show the evidence of magnetic phase transition in these samples. We think that two peaks contributed by the different oxygen-induced ferromagnetic phases resulted in the phase separation of the sample.