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We compute the equilibrium crystal structure and phase stability of iron at the α(bcc)-γ(fcc) phase transition as a function of temperature, by employing a combination of ab initio methods for calculating electronic band structures and dynamical mean-field theory. The magnetic correlation energy is found to be an essential driving force behind the α-γ structural phase transition in paramagnetic iron. [ABSTRACT FROM AUTHOR]

To explore the nature of the metallic state near the transition to a Mott insulator, we investigate the t-J model with random exchange interaction in d=∞ dimensions. A numerically exact solution is obtained by an extension of the continuous-time quantum Monte Carlo method to the case of a vector bosonic field coupled to a local spin. We show that the paramagnetic solution near the Mott insulator describes an incoherent metal with a residual moment, and that single-particle excitations produce an additional band, which is separated from the Mott-Hubbard band.

We calculate the spectra and spin susceptibilities of a Hubbard model with two bands having different bandwidths but the same on-site interaction, with parameters close to the orbital-selective Mott transition, using dynamical mean-field theory. If the Hund's rule coupling is sufficiently strong, one common energy scale emerges which characterizes both the location of kinks in the self-energy and extrema of the diagonal spin susceptibilities. A physical explanation of this energy scale is derived from a Kondo-type model. We infer that for multiband systems local spin dynamics rather than spectral functions determine the location of kinks in the effective band structure.

We introduce a well-defined and unbiased measure of the strength of correlations in quantum many-particle systems which is based on the relative von Neumann entropy computed from the density operator of correlated and uncorrelated states. The usefulness of this general concept is demonstrated by quantifying correlations of interacting electrons in the Hubbard model and in a series of transition-metal oxides using dynamical mean-field theory.

Employing a rigorous theoretical method for the construction of exact many-electron ground states we prove that interactions can be employed to tune a bare dispersive band structure such that it develops a flat band. Thereby, we show that pentagon-chain polymers with electron densities above half filling may be designed to become ferromagnetic or half metallic.

The magnetic ground state phase diagram of the disordered Hubbard model at half-filling is computed in dynamical mean-field theory supplemented with the spin resolved, typical local density of states. The competition between many-body correlations and disorder is found to stabilize paramagnetic and antiferromagnetic metallic phases at weak interactions. Strong disorder leads to Anderson localization of the electrons and suppresses the antiferromagnetic long-range order. Slater and Heisenberg antiferromagnets respond characteristically differently to disorder. The results can be tested with cold fermionic atoms loaded into optical lattices.

The effect of binary alloy disorder on the ferromagnetic phases of f-electron materials is studied within the periodic Anderson model. We find that disorder in the conduction band can drastically enhance the Curie temperature T{c} due to an increase of the local f moment. The effect may be explained qualitatively and even quantitatively by a simple theoretical ansatz. The emergence of an alloy Kondo insulator at noninteger filling is also pointed out.

Exact ground states of interacting electrons on the diamond Hubbard chain in a magnetic field are constructed which exhibit a wide range of properties such as flat-band ferromagnetism and correlation-induced metallic, half-metallic, or insulating behavior. The properties of these ground states can be tuned by changing the magnetic flux, local potentials, or electron density.

The phase diagram of correlated, disordered electron systems is calculated within dynamical mean-field theory using the geometrically averaged ("typical") local density of states. Correlated metal, Mott insulator, and Anderson insulator phases, as well as coexistence and crossover regimes, are identified. The Mott and Anderson insulators are found to be continuously connected.

We present a class of exact ground states of a three-dimensional periodic Anderson model at 3/4 filling. Hopping and hybridization of d and f electrons extend over the unit cell of a general Bravais lattice. Employing novel composite operators combined with 55 matching conditions the Hamiltonian is cast into positive semidefinite form. A product wave function in position space allows one to identify stability regions of an insulating and a conducting ground state. The metallic phase is a non-Fermi liquid with one dispersing and one flat band.

A detailed study of the paramagnetic to ferromagnetic phase transition in the one-band Hubbard model in the presence of binary-alloy disorder is presented. The influence of the disorder (with concentrations x and 1-x of the two alloy ions) on the Curie temperature T(c) is found to depend strongly on electron density n. While at high densities, n>x, the disorder always reduces T(c); at low densities, n

The electronic properties of paramagnetic V2O3 are investigated by the computational scheme LDA+DMFT(QMC). This approach merges the local density approximation (LDA) with dynamical mean-field theory (DMFT) and uses quantum Monte Carlo simulations (QMC) to solve the effective Anderson impurity model of DMFT. Starting with the crystal structure of metallic V2O3 and insulating (V0.962Cr0.038)2O3 we find a Mott-Hubbard transition at a Coulomb interaction U approximately 5 eV. The calculated spectrum is in very good agreement with experiment. Furthermore, the orbital occupation and the spin state S = 1 determined by us agree with recent polarization dependent x-ray-absorption experiments.