Spin and charge ordering in three-leg ladders in oxyborates

We study the spin ordering within the three-leg ladders present in the oxyborate Fe3O2BO3 consisting of localized classical spins interacting with conduction electrons (one electron per rung). We also consider the competition with antiferromagnetic superexchange interactions to determine the magnetic phase diagram. Besides a ferromagnetic phase we find (i) a phase with ferromagnetic rungs ordered antiferromagnetically and (ii) a zigzag canted spin ordering along the legs. We also determine the induced charge ordering within the different phases and the interplay with lattice instability. Our model is discussed in connection with the lattice dimerization transition observed in this system, emphasizing the role of the magnetic structure.     

Double-exchange model: phase separation versus canted spins

We study the competition between different possible ground states of the double-exchange model with strong ferromagnetic exchange interaction between itinerant electrons and local spins. Both for classical and quantum treatment of the local spins the homogeneous canted state is shown to be unstable against a phase separation. The conditions for the phase separation into the mixture of the antiferromagnetic and ferromagnetic/canted states are given. We also discuss another possible realization of the phase-separated state: ferromagnetic polarons embedded into an antiferromagnetic surrounding. The general picture of a percolated state, which emerges from these considerations, is discussed and compared with results of recent experiments on doped manganaties. Received 17 March 1999     

Quantized transport in two-dimensional spin-ordered structures

We study in detail the transport properties of a model of conducting electrons in the presence of double exchange between localized spins arranged on a 2D Kagome lattice, as introduced by Ohgushi, Murakami and Nagaosa. The relationship between the canting angle of the spin texture θ and the Berry phase field flux per triangular plaquette φ is derived explicitly and we emphasize the similarities between this model and Haldane's honeycomb lattice version of the quantum Hall effect. The quantization of the transverse (Hall) conductivity σ _xy is derived explicitly from the Kubo formula and a direct calculation of the longitudinal conductivity σ _xx shows the existence of a metal–insulator transition as a function of the canting angle θ (or flux density φ). This transition might be linked to that observable in the manganite compounds or in the pyrochlore ones, as the spin ordering changes from ferromagnetic to canted.     

Spin, charge and lattice couplings in Cu-deficient oxysulphide BiOCu0.94S

The electrical and magnetic properties of slightly Cu-deficient BiOCu(0.94)S are investigated using neutron diffraction, ac magnetic susceptibility, magnetization and electrical resistivity measurements. The Cu spins order in a ferromagnetic arrangement below T(C) = 250 K. An antiferromagnetic component develops below 180 K when the crystalline unit cell experiences a sharp thermal contraction upon cooling, resulting in a canted ferromagnetic spin arrangement at low temperatures. In the magnetically ordered state the electrical transport can be described using three-dimensional variable range hopping conduction. An applied magnetic field can effectively reduce the hopping barrier. Spin-charge couplings are clearly revealed when the resistivity departs from the hopping conduction and begins to increase with increasing temperatures above 250 K where the Cu spins become disordered.     

Novel aspects of charge and lattice dynamics in the hole-doped manganite La0.67Sr0.33MnO3

Previous infrared studies on the hole-doped manganite La_0.67Sr_0.33MnO₃ (LSMO) have analysed its charge dynamics in terms of one type of charge carrier despite evidence of both electron and hole Fermi surfaces. Here, we investigate the charge dynamics of an LSMO film with infrared and optical spectroscopy in order to provide a complete picture of metallic conduction. In the ferromagnetic metallic phase, the low-frequency optical conductivity is best explained by a two-carrier model comprising electrons and holes. The number densities, effective masses and relaxation response of the delocalized electrons and holes are quantified. We discover that only one-third of the doped charges are coherent and contribute to the dc transport. Metallic LSMO cannot be classified as a bad metal at low temperatures because the mean free path of the coherent, mobile charge carriers exceeds the Ioffe–Regel–Mott limit. The incoherent spectral response of the doped charges manifests itself as a broad mid-infrared feature. We also report the first observation of splitting of an infrared-active phonon due to local Jahn–Teller distortion in the vicinity of the thermally driven transition to the nonmetallic, paramagnetic phase in LSMO. This demonstrates that infrared spectroscopy is capable of detecting the presence of local lattice distortions in correlated electron systems.     

Coexistence of antiferromagnetic and ferromagnetic phase for ferromagnetic Kondo lattice model

To study the proposed phase separations in doped manganites, we performed Monte-Carlo calculations for the ferromagnetic Kondo lattice model with strong Hund's coupling between conduction electrons and localized spins. For the practical calculations, we adopted a one dimensional lattice and treated the spins of the localized t_2g electrons semi-classically. A direct evidence of the phase separation is observed from a snapshot of the spatial dependence of localized spins. No indication of the canted or spiral phases is found in the results of simulations. Further, the calculated results of the spin structure factor in the phase separation region are well compared with recent experiments. Received: 1st September 1998 / Revised: 30 October 1998 / Accepted: 27 November 1998     

Anomalous magnetic field dependence of T AF in La 0.95 Sr 0.05 MnO 3

The magneto-elastic properties of single-crystalline La_0.95Sr_0.05MnO₃ have been studied ultrasonically. Our investigations focussed on the temperature interval where magnetic ordering starts to evolve and results in a spin canted antiferromagnetic ground state. In detail the experiments revealed that the magnetic order parameter in low-doped manganite is only weakly coupled to lattice strains. Furthermore, the anomalous temperature dependence of the order parameter as found resembles highly that in stoichiometric LaMnO₃. However, the main and most surprising finding is that external magnetic fields favor the spin canted phase in La_0.95Sr_0.05MnO₃. It is unclear at present how the exchange interaction can be tuned by magnetic fields in the way observed and we are not aware of existing theoretical concepts which might give a plausible explanation for the unexpected field dependent behavior of the critical temperature. We believe, however, that this behavior primarily results from the fact that the exchange interaction depends sensitively on the orbital configuration of the manganese d electrons. Received 27 March 2000     

Expulsion of charge carriers from quasi-two-dimensional antiferromagnetic structures and formation of spin-liquid droplets in them

In antiferromagnetic semiconductors the charge carrier energy decreases, when the long-range magnetic ordering is destroyed. This leads to the fact that in degenerate quasi-two-dimensional semiconductors to which high-TC superconductors belong, both the collinear and canted antiferromagnetic orderings are unstable at arbitrarily small charge carrier density, if the exchange between carriers and localized moments is not very weak. The condition for instability coincides with condition for formation of an electron self-trapped state inside a ferromagnetic region. This means that the antiferromagnetic structure expulses charge carriers into the ferromagnetic phase. An alternative to it is its expulsion into magnetically disordered phase. Then a new type of the carrier self-trapped state realizes when a carrier disorders magnetically a certain region in the antiferromagnet and stabilizes this region by its localization inside it. It corresponds to antiferromagnetic-spinliquid phase separation on the single-electron level. At sufficiently large carrier densities the canted antiferromagnetic structure induced by carriers may be, atleast, relatively stable.     

Delta doping of ferromagnetism in antiferromagnetic manganite superlattices

We demonstrate that delta doping can be used to create a dimensionally confined region of metallic ferromagnetism in an antiferromagnetic (AFM) manganite host, without introducing any explicit disorder due to dopants or frustration of spins. Theoretical consideration of these additional carriers shows that they cause a local enhancement of ferromagnetic double exchange with respect to AFM superexchange, resulting in local canting of the AFM spins. This leads to a highly modulated magnetization, as measured by polarized neutron reflectometry. The spatial modulation of the canting is related to the spreading of charge from the doped layer and establishes a fundamental length scale for charge transfer, transformation of orbital occupancy, and magnetic order in these manganites. Furthermore, we confirm the existence of the canted, AFM state as was predicted by de Gennes [Phys. Rev. 118, 141 (1960)] but had remained elusive.     

Magnetic ordering in granular system

The conditions of the formation of different magnetic structures with ferromagnetic (FM) and antiferromagnetic (AFM) ordering in granular materials containing a subsystem of ferromagnetic granules are considered within the phenomenological approach. It is supposed that the magnetostatic field and the exchange interaction between conduction electrons and magnetic ions are responsible for the formation of magnetic structure.     

Exchange bias tuned by cooling field in La0.2Ca0.8MnO3 nanoparticles

We report the magnetic properties in the nanosized charge ordering manganite La_0.2Ca_0.8MnO₃ with an average particle size ～50 nm. The sample exhibits ferromagnetism at low temperatures. The exchange bias phenomenon is observed when the sample is cooled down in an external magnetic field. Moreover, the exchange bias field is dependent on the cooling field and shows a maximum of ～520 Oe under a cooling field ～5 kOe. The exchange bias effect can be attributed to the exchange coupling between the ferromagnetic shell and antiferromagnetic core. The decrease of exchange bias field in high cooling field can be attributed to the growth of ferromagnetic component under high cooling field.     

Effect of Y-doping on the magnetic and charge orderings in Nd2/3Ca1/3MnO3

The shifts of the magnetic and charge ordering transition temperatures caused by Nd substitution for Y in Nd_2/3Ca_1/3MnO₃ CMR narrow-band perovskite manganite have been studied. At low temperatures, three different long-range magnetic orderings consistent with a phase separation scenario have been observed in the doped compound (Nd_0.9Y_0.1)_2/3Ca_1/3MnO₃ by neutron-diffraction study: the antiferromagnetic orderings of PCE and DE types existing below ∼110 and ∼60 K, respectively, and the ferromagnetic one of B type existing below ∼42. Magnetic phase transformations temperatures as well as those of charge ordering have been found to be structural-dependent. Y-doping leads to the decrease of the anisotropy of the orthorhombic Pnma crystal lattice b/√2c, which causes a decrease of the indirect exchange parameters in the system and thus a decrease in the magnetic transformation temperatures for 20-30 K in the doped compound. Doping leads as well to the higher level of the coherent Jahn-Teller distortions of the MnO₆ octahedra in the 200-300 K temperature region, which results in the increase of the charge ordering temperature for ∼80 K.     

Electron leakage and double-exchange ferromagnetism at the interface between a metal and an antiferromagnetic insulator: CaRuO3/CaMnO3

Density-functional electronic structure studies of a prototype interface between a paramagnetic metal and an antiferromagnetic (AFM) insulator (CaRuO(3)/CaMnO(3)) reveal the exponential leakage of the metallic electrons into the insulator side. The leaked electrons in turn control the magnetism at the interface via the ferromagnetic (FM) Anderson-Hasegawa double exchange, which competes with the AFM superexchange of the bulk CaMnO3. The competition produces a FM interfacial CaMnO3 layer (possibly canted); but beyond this layer, the electron penetration is insufficient to alter the bulk magnetism.     

Ferromagnetic ground state in the Kondo lattice model

We present a series of rigorous examples of the Kondo lattice model that exhibit full ferromagnetism in the ground state. The models are defined in one-, two- and three-dimensional lattices, and are characterized by a range of hopping terms, specific electron filling, and large ferromagnetic coupling. Our examples show that a sufficient strong but finite exchange coupling between conduction electrons and localized spins could overcome the competition from mobility of a finite density of electrons and drive the system from a paramagnetic phase to a ferromagnetic phase. We also establish a relation of ferromagnetism between the Hubbard model and Kondo lattice model. Meanwhile some rigorous results on ferromagnetism in the corresponding Hubbard model are presented. Received: 10 September 1997 / Revised: 15 October 1997 / Accepted: 17 October 1997     

Effect of strong electron correlations and electron-lattice interaction on the ordering of electron orbitals

The interactions between electrons in degenerate orbitals and between electrons and the lattice degrees of freedom have been treated by the Monte Carlo method taking into account the anharmonicity of ionic vibrations in the framework of the phenomenological model. The existence regions of the ferromagnetic and antiferromagnetic orbital orders have been found. Two critical temperatures have been determined at which the long-range orbital order disappears and the distribution of electrons over the orbitals becomes uniform. The correlation between the orbital ordering types and the thermal expansion coefficient has been established. It has been found that an increase in anharmonicity leads to the stabilization of the antiferromagnetic orbital ordering.     

Phase separation in a manganite La<Subscript>0.95</Subscript>Ba<Subscript>0.05</Subscript>MnO<Subscript>3</Subscript> crystal

The structure and magnetic states of a crystal of lightly doped manganite La_0.95Ba_0.05MnO₃ were studied using thermal-neutron diffraction, magnetic measurements, and electrical resistance data in a wide temperature range. It is shown that, in terms of its magnetic properties, the orthorhombic crystal is characterized by two order parameters, namely, antiferromagnetic (T _N = 123.6 K) and ferromagnetic (T _C = 136.7 K). The results obtained differ in detail from known information on the manganites La_0.95Ca_0.05MnO₃ and La_0.94Sr_0.06MnO₃. Two models of the magnetic state of the La_0.95Ba_0.05MnO₃ crystal are discussed, one of which is a model of a canted antiferromagnetic spin system and another is associated with the phase separation of the manganite. Arguments are advanced in favor of the coexistence in this crystal of the antiferromagnetic phase (about 87%) with a Mn⁴⁺ ion concentration of 0.048 and the 1/16-type charge-ordered ferromagnetic phase (about 13%) with a Mn⁴⁺ ion concentration of 0.0625. The specific features of the manganite studied are due to self-organization of the La_0.95Ba_0.05MnO₃ crystal lattice caused by the relatively large barium ion size.     

Unusual ferromagnetism in nanoparticles of doped oxides and manganites

The observation of unusually large ferromagnetism in the nanoparticles of doped oxides and enhanced ferromagnetic tendencies in manganite nanoparticles have been in focus recently. For the transition metal doped oxide nanoparticles a phenomenological ‘charge transfer ferromagnetism’ model has been recently proposed by Coey et al. From a microscopic calculation with charge transfer between the defect band and mixed valent dopants, acting as reservoir, we show how the unusually high ferromagnetic response develops. The puzzle of nanosize-induced ferromagnetic tendencies in manganites is also addressed within the same framework where lattice imperfections and uncompensated charges at the surface of the nanoparticle are shown to reorganize the surface electronic structures with enhanced double exchange.     

The effect of band Jahn-Teller distortion on the magnetoresistivity of manganites: a model study

We present a model study of magnetoresistance through the interplay of magnetisation, structural distortion and external magnetic field for the manganite systems. The manganite system is described by the Hamiltonian which consists of the s-d type double exchange interaction, Heisenberg spin-spin interaction among the core electrons, and the static and dynamic band Jahn-Teller (JT) interaction in the e(g) band. The relaxation time of the e(g) electron is found from the imaginary part of the Green's function using the total Hamiltonian consisting of the interactions due to the electron and phonon. The calculated resistivity exhibits a peak in the pure JT distorted insulating phase separating the low temperature metallic ferromagnetic phase and the high temperature paramagnetic phase. The resistivity is suppressed with the increase of the external magnetic field. The e(g) electron band splitting and its effect on magnetoresistivity is reported here.     

Helicoidal ordering in iron perovskites

We study the double exchange in transition metal oxides with itinerant and localized electrons. We show that the charge transfer energy Delta and the oxygen-oxygen hopping amplitude t(pp) have a strong effect on magnetic ordering: while for Delta>0 the ground state is ferromagnetic, for negative Delta and large t(pp) the double exchange gives rise to an incommensurate helicoidal ordering of local spins, observed, e.g., in the iron perovskites SrFeO3 and CaFeO3. For negative Delta, the metal-insulator transition into a charge-ordered state has little effect on magnetic ordering. This explains the difference in magnetic and transport properties of ferrates and manganites.