We review the dynamical mean-field theory of strongly correlated electron systems which is based on a mapping of lattice models onto quantum impurity models subject to a self-consistency condition. This mapping is exact for models of correlated electrons in the limit of large lattice coordination (or infinite spatial dimensions). It extends the standard mean-field construction from classical statistical mechanics to quantum problems. We discuss the physical ideas underlying this theory and its mathematical derivation. Various analytic and numerical techniques that have been developed recently in order to analyze and solve the dynamical mean-field equations are reviewed and compared to each other. The method can be used for the determination of phase diagrams (by comparing the stability of various types of long-range order), and the calculation of thermodynamic properties, one-particle Green's functions, and response functions. We review in detail the recent progress in understanding the Hubbard model and the Mott metal-insulator transition within this approach, including some comparison to experiments on three-dimensional transition-metal oxides. We present an overview of the rapidly developing field of applications of this method to other systems. The present limitations of the approach, and possible extensions of the formalism are finally discussed. Computer programs for the numerical implementation of this method are also provided with this article.

Dynamical mean-field theory of strongly correlated fermion systems and the limit of infinite dimensions

Multiferroic magnetoelectrics are materials that are both ferromagnetic and ferroelectric in the same phase. As a result, they have a spontaneous magnetization that can be switched by an applied magnetic field, a spontaneous polarization that can be switched by an applied electric field, and often some coupling between the two. Very few exist in nature or have been synthesized in the laboratory. In this paper, we explore the fundamental physics behind the scarcity of ferromagnetic ferroelectric coexistence. In addition, we examine the properties of some known magnetically ordered ferroelectric materials. We find that, in general, the transition metal d electrons, which are essential for magnetism, reduce the tendency for off-center ferroelectric distortion. Consequently, an additional electronic or structural driving force must be present for ferromagnetism and ferroelectricity to occur simultaneously.

Why Are There so Few Magnetic Ferroelectrics

http://sces.phys.utk.edu/mostcited/mc1_1114.pdf

Colossal Magnetoresistant Materials: The Key Role of Phase Separation

Colossal magnetoresistance1—an unusually large change of resistivity observed in certain materials following application of magnetic field—has been extensively researched in ferromagnetic perovskite manganites. But it remains unclear why the magnetoresistive response increases dramatically when the Curie temperature (T C) is reduced. In these materials, T C varies sensitively with changing chemical pressure; this can be achieved by introducing trivalent rare-earth ions of differing size into the perovskite structure2,3,4, without affecting the valency of the Mn ions. The chemical pressure modifies local structural parameters such as the Mn–O bond distance and Mn–O–Mn bond angle, which directly influence the case of electron hopping between Mn ions (that is, the electronic bandwidth). But these effects cannot satisfactorily explain the dependence of magnetoresistance on T C. Here we demonstrate, using electron microscopy data, that the prototypical (La,Pr,Ca)MnO3 system is electronically phase-separated into a sub-micrometre-scale mixture of insulating regions (with a particular type of charge-ordering) and metallic, ferromagnetic domains. We find that the colossal magnetoresistive effect in low-T C systems can be explained by percolative transport through the ferromagnetic domains; this depends sensitively on the relative spin orientation of adjacent ferromagnetic domains which can be controlled by applied magnetic fields.

Percolative phase separation underlies colossal magnetoresistance in mixed-valent manganites

We review recent experimental work falling under the broad classification of colossal magnetoresistance (CMR), which is magnetoresistance associated with a ferromagnetic-toparamagnetic phase transition. The prototypical CMR compound is derived from the parent compound, perovskite LaMnO 3. When hole doped at a concentration of 20–40% holes/Mn ion, for instance by Ca or Sr substitution for La, the material displays a transition from a high-temperature paramagnetic insulator to a low-temperature ferromagnetic metal. Near the phase transition temperature, which can exceed room temperature in some compositions, large magnetoresistance is observed and its possible application in magnetic recording has revived interest in these materials. In addition, unusual magneto-elastic effects and charge ordering have focused attention on strong electron–phonon coupling. This coupling, which is a type of dynamic extended-system version of the Jahn–Teller effect, in conjunction with the double-exchange interaction, is also viewed as essential for a microscopic description of CMR in the manganite perovskites. Large magnetoresistance is also seen in other systems, namely Tl 2Mn2O7 and some Cr chalcogenide spinels, compounds which differ greatly from the manganite perovskites. We describe the relevant points of contrast between the various CMR materials.

REVIEW ARTICLE: Colossal magnetoresistance

Pressure response device

Articles according to the invention comprise a superconductive cuprate (e.g., YBa 2 Cu 3 O 7 ) body containing elongate grains measuring at least about 10 μm along the long axis and having an aspect ratio of at least 10:1. Bodies according to the invention can have relatively high critical current density, as compared to analogous non-textured bodies.

Article comprising textured superconductive cuprate material

Production of superconductor

Significantly improved flux-pinning has been achieved in bulk YBa2Cu3O7-δ superconductor (‘123’ compound) containing fine-scale defects (<~50 A thick). The measured Jc(magn.) of ~l05 A/cm2 at 77K, H = 0.9T is about ten times higher than the typical values for bulk Y-Ba-Cu-O. The improved structure was produced by rapid decomposition at 920°C of the YBa2Cu4O8 (‘124’) precursor.

Significantly Enhanced Flux-Pinning in Y-Ba-Cu-O by Simple Processing

Some mechanical, electrical, and thermal properties of high T c superconductors such as (Ba, Y) cuprates can be substantially improved by the dispersal of an appropriate metal in the superconductive body. For instance, mixing Ag particles with superconductive powder of nominal composition Ba2YCu3O7 and processing the mixture in the conventional manner can produce superconductive bodies having T c of about 93K and substantially greater fracture strength and normal state electrical and thermal conductivity than otherwise identical bodies that do not contain Ag particles.

Thomas Henry Tiefel

Papers

Pressure response device

Article comprising textured superconductive cuprate material

Production of superconductor

Significantly Enhanced Flux-Pinning in Y-Ba-Cu-O by Simple Processing

Superconductive body having improved properties, and apparatus and systems comprising such a body